CN100391945C - S-(-)-indolyl-2-carboxylic acid synthesizing method - Google Patents
S-(-)-indolyl-2-carboxylic acid synthesizing method Download PDFInfo
- Publication number
- CN100391945C CN100391945C CNB2005100498874A CN200510049887A CN100391945C CN 100391945 C CN100391945 C CN 100391945C CN B2005100498874 A CNB2005100498874 A CN B2005100498874A CN 200510049887 A CN200510049887 A CN 200510049887A CN 100391945 C CN100391945 C CN 100391945C
- Authority
- CN
- China
- Prior art keywords
- carboxylic acid
- indoline
- solvent
- reaction
- synthetic method
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 238000000034 method Methods 0.000 title abstract description 4
- 230000002194 synthesizing effect Effects 0.000 title 1
- 238000010189 synthetic method Methods 0.000 claims abstract description 31
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 claims abstract description 28
- 229960005190 phenylalanine Drugs 0.000 claims abstract description 14
- 239000002994 raw material Substances 0.000 claims abstract description 13
- 239000002904 solvent Substances 0.000 claims description 38
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 36
- QNRXNRGSOJZINA-QMMMGPOBSA-N (2s)-2,3-dihydro-1h-indole-2-carboxylic acid Chemical compound C1=CC=C2N[C@H](C(=O)O)CC2=C1 QNRXNRGSOJZINA-QMMMGPOBSA-N 0.000 claims description 35
- 238000006243 chemical reaction Methods 0.000 claims description 29
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 claims description 20
- 238000001035 drying Methods 0.000 claims description 18
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 18
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 claims description 16
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 14
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 14
- 239000011734 sodium Substances 0.000 claims description 14
- 229910052708 sodium Inorganic materials 0.000 claims description 14
- 238000007363 ring formation reaction Methods 0.000 claims description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 12
- 238000005660 chlorination reaction Methods 0.000 claims description 12
- 238000006722 reduction reaction Methods 0.000 claims description 12
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 10
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims description 10
- 239000000460 chlorine Substances 0.000 claims description 10
- 229910052801 chlorine Inorganic materials 0.000 claims description 10
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical group Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 230000009467 reduction Effects 0.000 claims description 8
- QDGAVODICPCDMU-UHFFFAOYSA-N 2-amino-3-[3-[bis(2-chloroethyl)amino]phenyl]propanoic acid Chemical compound OC(=O)C(N)CC1=CC=CC(N(CCCl)CCCl)=C1 QDGAVODICPCDMU-UHFFFAOYSA-N 0.000 claims description 7
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 6
- 238000013019 agitation Methods 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 6
- 150000001879 copper Chemical class 0.000 claims description 6
- 239000013078 crystal Substances 0.000 claims description 6
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 6
- 238000005406 washing Methods 0.000 claims description 6
- 229960003280 cupric chloride Drugs 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 4
- 230000035484 reaction time Effects 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- 229910021591 Copper(I) chloride Inorganic materials 0.000 claims description 3
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 claims description 3
- 229940045803 cuprous chloride Drugs 0.000 claims description 3
- 150000004820 halides Chemical class 0.000 claims description 3
- 230000000694 effects Effects 0.000 claims description 2
- 230000003301 hydrolyzing effect Effects 0.000 claims description 2
- 238000010992 reflux Methods 0.000 claims description 2
- 239000013557 residual solvent Chemical group 0.000 claims description 2
- 230000008901 benefit Effects 0.000 abstract description 2
- 230000008569 process Effects 0.000 abstract description 2
- 238000003912 environmental pollution Methods 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 16
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 12
- 238000002360 preparation method Methods 0.000 description 12
- 239000003208 petroleum Substances 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- 230000006872 improvement Effects 0.000 description 7
- 230000007062 hydrolysis Effects 0.000 description 5
- 238000006460 hydrolysis reaction Methods 0.000 description 5
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
- 229910001628 calcium chloride Inorganic materials 0.000 description 4
- 239000001110 calcium chloride Substances 0.000 description 4
- 230000006837 decompression Effects 0.000 description 4
- 229960000935 dehydrated alcohol Drugs 0.000 description 4
- 238000003810 ethyl acetate extraction Methods 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000004576 sand Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 238000010792 warming Methods 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 3
- 229960004756 ethanol Drugs 0.000 description 2
- QNRXNRGSOJZINA-UHFFFAOYSA-N indoline-2-carboxylic acid Chemical compound C1=CC=C2NC(C(=O)O)CC2=C1 QNRXNRGSOJZINA-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- IPVQLZZIHOAWMC-QXKUPLGCSA-N perindopril Chemical compound C1CCC[C@H]2C[C@@H](C(O)=O)N(C(=O)[C@H](C)N[C@@H](CCC)C(=O)OCC)[C@H]21 IPVQLZZIHOAWMC-QXKUPLGCSA-N 0.000 description 1
- 229960002582 perindopril Drugs 0.000 description 1
- LOAUVZALPPNFOQ-UHFFFAOYSA-N quinaldic acid Chemical compound C1=CC=CC2=NC(C(=O)O)=CC=C21 LOAUVZALPPNFOQ-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Indole Compounds (AREA)
Abstract
The present invention discloses a synthetic method for (S)-(-)-indolyl-2-carboxylic acid. The (S)-(-)-indolyl-2-carboxylic acid is prepared by chlorinating, cyclizing and reducing the main initial raw material of L-phenylalanine. The synthetic method for (S)-(-)-indolyl-2-carboxylic acid of the present invention has the advantages of no environmental pollution, simple process, low cost and high yield.
Description
Technical field
The present invention relates to a kind of synthetic method of organic compound, particularly the synthetic method of S-(-)-indoline-2-carboxylic acid.
Background technology
S-(-)-indoline-2-carboxylic acid of molecular formula shown in S-1 is the key intermediate of synthetic drugs PERINDOPRIL (molecular formula is shown in S-2).The synthetic method of S-(-)-indoline-2-carboxylic acid is domestic does not still have bibliographical information, and external pertinent literature is also rare.U.S. Pat 4914214, USP4508729 has related to the synthetic method of this material, all be raw material with the Indoline-2-carboxylic acid, obtains splitting behind the racemize indoline-2-carboxylic acid through esterification, reduction, hydrolysis.But these methods all exist expensive raw material price, the not high defective of the chiral purity of resolved product and yield.
Summary of the invention
At the deficiencies in the prior art part, the invention provides the synthetic method of a kind of environmental friendliness, technology is simple, cost is low, yield is high S-(-)-indoline-2-carboxylic acid.
The present invention is for reaching above purpose, and be to realize by such technical scheme: the synthetic method that a kind of S-(-)-indoline-2-carboxylic acid is provided: with the L-phenylalanine is raw material, may further comprise the steps successively:
1), chlorination: with L-phenylalanine, solvent and ethanol under agitation condition, feed chlorine and carry out chlorination reaction, the weight ratio of L-phenylalanine and solvent is 1: 7～1: 12, consumption of ethanol is 10%～31% of a L-phenylalanine amount of substance, temperature of reaction is 10～30 ℃, and the reaction times is 0.5～2 hour; With the hydrochloride crystal of described chlorination reaction gained be hydrolyzed successively, vacuum removal solvent, washing, drying step, L-2,4-dichlorobenzene L-Ala;
2), cyclization: with above-mentioned L-2,4-dichlorobenzene L-Ala carries out ring-closure reaction in solvent, under the effect of copper salt catalyst, L-2, and the weight ratio of 4-dichlorobenzene L-Ala and solvent is 1: 1～1: 3, the weight of copper salt catalyst is L-2,5%～15% of 4-dichlorobenzene L-Ala; Temperature of reaction is 100～140 ℃, 2～6 hours reaction times; After reaction finishes, extract successively again, wash, dry, remove solvent step, S-indoline-6-chloro-2-carboxylic acid;
3), reduction: above-mentioned S-indoline-6-chloro-2-carboxylic acid and sodium, the trimethyl carbinol are carried out back flow reaction in solvent, the weight ratio of described S-indoline-6-chloro-2-carboxylic acid and solvent is 1: 4～1: 8.2, and the consumption of the sodium and the trimethyl carbinol is 1～3 times of amount of substance of S-indoline-6-chloro-2-carboxylic acid; Solvent step is filtered, removed to reaction after finishing again successively.
A kind of improvement as S-of the present invention (-)-indoline-2-carboxylic acid synthetic method: earlier S-indoline-6-chloro-2-carboxylic acid is mixed with partial solvent in the reduction reaction of step 3), be made into concentration and be S-indoline-6-chloro-2-carboxylic acid solution of 49%, described S-indoline-6-chloro-2-carboxylic acid solution is added in the mixture that sodium, the trimethyl carbinol, residual solvent forms in the mode that drips carry out back flow reaction again.
Further improvement as S-of the present invention (-)-indoline-2-carboxylic acid synthetic method: the reflux time of step 3) is 2～6 hours.
Further improvement as S-of the present invention (-)-indoline-2-carboxylic acid synthetic method: be hydrolyzed with frozen water in the hydrolysing step of step 1).
Further improvement as S-of the present invention (-)-indoline-2-carboxylic acid synthetic method: solvent for use is a halides in the chlorination reaction of step 1), for example chloroform or tetracol phenixin.
As S-of the present invention (-)-draw the further improvement of diindyl quinoline-2-carboxylic acid synthetic method: used copper salt catalyst is cupric chloride or cuprous chloride in ring-closure reaction step 2).
Further improvement as S-of the present invention (-)-indoline-2-carboxylic acid synthetic method: solvent for use is a diethanolamine in ring-closure reaction step 2).
Further improvement as S-of the present invention (-)-indoline-2-carboxylic acid synthetic method: solvent for use is a tetrahydrofuran (THF) in the reduction reaction of step 3).
Reaction formula is as follows:
The synthetic method of S-of the present invention (-)-indoline-2-carboxylic acid, with chiral organic compound---the L-phenylalanine is a raw material, through the synthetic S-(-) of superchlorination, cyclization and reduction three-step reaction-indoline-2-carboxylic acid.Route of the present invention, has omitted splitting step, has simplified technological operation so building-up process does not need to split because to have adopted the compound that has an identical configuration with target product be raw material.Raw material L-phenylalanine at present can scale operation, therefore can reduce production costs.The synthetic method of S-of the present invention (-)-indoline-2-carboxylic acid is compared with the technology that in the past synthetic racemic modification splits again, have that operational path is short, yield is high (in the L-phenylalanine, high energy reaches 36.5%), the advantage that the products obtained therefrom optical activity is high.
Embodiment
Raw material L-phenylalanine specific rotation is
(c=2.0, H
2O)
The synthetic method of embodiment 1:S-(-)-indoline-2-carboxylic acid is main starting raw material with the L-phenylalanine, makes through following step successively:
(1) chlorination, i.e. L-2, the preparation of 4-dichlorobenzene L-Ala:
Add 208g (1.26mol) L-phenylalanine and 1600g in the there-necked flask of 2000ml with the dry tetracol phenixin of crossing of Calcium Chloride Powder Anhydrous, add 7.2ml (0.126mol) dehydrated alcohol again, under agitation condition, feed chlorine about 10 ℃, begin to separate out crystal of hydrochloride this moment, continue to stop to feed behind the logical chlorine 1h.The gas except that HCl is caught up with in heating, adds 400ml frozen water hydrolysis hydrochloride again; Separate out L-2 behind the vacuum removal solvent, 4-dichlorobenzene L-Ala solid, the petroleum ether after drying gets this step product 130g, 243～245 ℃ of fusing points (dec.), yield 44%.
(2) cyclization, the i.e. preparation of S-indoline-6-chloro-2-carboxylic acid:
Add diethanolamine 100g in the 1000ml there-necked flask, cupric chloride 5g adds 100g (0.42mol) L-2 after stirring is warming up to 100 ℃ in batches, and 4-dichlorobenzene L-Ala after the dissolving, keeps 100 ℃ to continue reaction 4h fully.Finish the reaction back with the 200ml ethyl acetate extraction, extraction phase with the 100ml water washing after with anhydrous sodium sulfate drying, decompression removes solvent, get pale solid-S-indoline-6-chloro-2-carboxylic acid, the petroleum ether after drying, get this step product 25g, 203～204 ℃ of fusing points (dec.), yield 30%.
(3) reduction, i.e. the preparation of S-(-)-indoline-2-carboxylic acid:
Add 75g tetrahydrofuran (THF) and 8.5g (0.37mol) sodium sand in the 500ml there-necked flask, add the new trimethyl carbinol 27.5g (0.37mol) that steams under the violent stirring and make mixture.At this moment, Dropwise 5 0g is dissolved with the tetrahydrofuran solution of 24.5g (0.125mol) S-indoline-6-chloro-2-carboxylic acid (promptly by the tetrahydrofuran (THF) mixing gained of 24.5g S-indoline-6-chloro-2-carboxylic acid with 25.5g in said mixture in 30 minutes, concentration is S-indoline-6-chloro-2-carboxylic acid solution of 49%), back flow reaction 2 hours.Reaction finishes after-filtration and removes unreacted sodium, remove behind the solvent product S-(-)-indoline-2-carboxylic acid, drying, the 14g product, 184～186 ℃ of fusing points,
(c=1.0, DMSO), yield 68.3%.
The synthetic method of embodiment 2:S-(-)-indoline-2-carboxylic acid is main starting raw material with the L-phenylalanine, makes through following step successively:
(1) chlorination, i.e. L-2, the preparation of 4-dichlorobenzene L-Ala:
Add 208g (1.26mol) L-phenylalanine and 2000g in the there-necked flask of 2000ml with the dry tetracol phenixin of crossing of Calcium Chloride Powder Anhydrous, add 14.4ml (0.256mol) dehydrated alcohol again, under agitation condition, feed chlorine about 20 ℃, begin to separate out crystal of hydrochloride this moment, continue to stop to feed behind the logical chlorine 1.5h.The gas except that HCl is caught up with in heating, adds 400ml water hydrolysis hydrochloride again.Separate out L-2 behind the vacuum removal solvent, 4-dichlorobenzene L-Ala solid, the petroleum ether after drying gets this step product 188g, 243～245 ℃ of fusing points (dec.), yield 63.2%.
(2) cyclization, the i.e. preparation of S-indoline-6-chloro-2-carboxylic acid:
Add diethanolamine 200g in the 1000ml there-necked flask, cupric chloride 10g adds 100g (0.42mol) L-2 after stirring is warming up to 100 ℃ in batches, and 4-dichlorobenzene L-Ala after the dissolving, keeps 120 ℃ to continue reaction 2h fully.Finish the reaction back with the 200ml ethyl acetate extraction, extraction phase with the 100ml water washing after with anhydrous sodium sulfate drying, decompression removes solvent, get pale solid-S-indoline-6-chloro-2-carboxylic acid, the petroleum ether after drying, get this step product 28g, 203～204 ℃ of fusing points (dec.), yield 33.4%.
(3) reduction, i.e. the preparation of S-(-)-indoline-2-carboxylic acid:
Add 125g tetrahydrofuran (THF) and 2.88g (0.125mol) sodium sand in the 500ml there-necked flask, add the new trimethyl carbinol 9.25g (0.125mol) that steams under the violent stirring.At this moment, Dropwise 5 0g is dissolved with the tetrahydrofuran solution of 24.5g (0.125mol) S-indoline-6-chloro-2-carboxylic acid, back flow reaction 4 hours in 30 minutes.Reaction finishes after-filtration and removes unreacted sodium, remove behind the solvent product S-(-)-indoline-2-carboxylic acid, drying, the 9g product, 184～186 ℃ of fusing points,
(c=1.0, DMSO), yield 43.9%.
The synthetic method of embodiment 3:S-(-)-indoline-2-carboxylic acid is main starting raw material with the L-phenylalanine, makes through following step successively:
(1) chlorination, i.e. L-2, the preparation of 4-dichlorobenzene L-Ala:
Add 104g (0.63mol) L-phenylalanine and 1200g in the there-necked flask of 1000ml with the dry tetracol phenixin of crossing of Calcium Chloride Powder Anhydrous, add 10.8ml (0.192mol) dehydrated alcohol again, under agitation condition, feed chlorine about 30 ℃, begin to separate out crystal of hydrochloride this moment, continue to stop to feed behind the logical chlorine 2h.The gas except that HCl is caught up with in heating, adds 200ml water hydrolysis hydrochloride again.Separate out L-2 behind the vacuum removal solvent, 4-dichlorobenzene L-Ala solid, the petroleum ether after drying gets this step product 108g, 243～245 ℃ of fusing points (dec.), yield 72.6%.
(2) cyclization, the i.e. preparation of S-indoline-6-chloro-2-carboxylic acid:
Add diethanolamine 300g in the 1000ml there-necked flask, cupric chloride 15g adds 100g (0.42mol) L-2 after stirring is warming up to 100 ℃ in batches, and 4-dichlorobenzene L-Ala after the dissolving, keeps 140 ℃ of back flow reaction 6h fully.Finish the reaction back with the 200ml ethyl acetate extraction, extraction phase with the 100ml water washing after with anhydrous sodium sulfate drying, decompression removes solvent, get pale solid-S-indoline-6-chloro-2-carboxylic acid, the petroleum ether after drying, get this step product 54g, 203～204 ℃ of fusing points (dec.), yield 64.4%.
(3) reduction, i.e. the preparation of S-(-)-indoline-2-carboxylic acid
Add 350g tetrahydrofuran (THF) and 11.5g (0.5mol) sodium sand in the 1000ml there-necked flask, add the new trimethyl carbinol 37g (0.5mol) that steams under the violent stirring.At this moment, in 30 minutes, drip the tetrahydrofuran solution that 100g is dissolved with 49g (0.25mol) S-indoline-6-chloro-2-carboxylic acid, back flow reaction 6 hours.Reaction finishes after-filtration and removes unreacted sodium, remove behind the solvent product S-(-)-indoline-2-carboxylic acid, drying, the 32g product, 180～182 ℃ of fusing points,
(c=1.0, DMSO), yield 78.0%.
Embodiment 4: the synthetic method of a kind of S-(-)-indoline-2-carboxylic acid is main starting raw material with the L-phenylalanine, makes through following step successively:
(1) chlorination, i.e. L-2, the preparation of 4-dichlorobenzene L-Ala
Add 208g (1.26mol) L-phenylalanine and 1600g in the there-necked flask of 2000ml with the dry chloroform of crossing of Calcium Chloride Powder Anhydrous, add 7.2ml (0.126mol) dehydrated alcohol again, under agitation condition, feed chlorine about 20 ℃, begin to separate out crystal of hydrochloride this moment, continue to stop to feed behind the logical chlorine 0.5h.The gas except that HCl is caught up with in heating, adds 200ml water hydrolysis hydrochloride again.Separate out L-2 behind the vacuum removal solvent, 4-dichlorobenzene L-Ala solid, the petroleum ether after drying gets this step product 120g, 243～245 ℃ of fusing points (dec.), yield 40.4%.
(2) cyclization, the i.e. preparation of S-indoline-6-chloro-2-carboxylic acid
Add diethanolamine 100g in the 1000ml there-necked flask, cuprous chloride 10g adds 100g (0.42mol) L-2 after stirring is warming up to 100 ℃ in batches, and 4-dichlorobenzene L-Ala after the dissolving, keeps 100 ℃ to continue reaction 4h fully.Finish the reaction back with the 200ml ethyl acetate extraction, extraction phase with the 100ml water washing after with anhydrous sodium sulfate drying, decompression removes solvent, get pale solid-S-indoline-6-chloro-2-carboxylic acid, the petroleum ether after drying, get this step product 37g, 203～204 ℃ of fusing points (dec.), yield 44.2%.
(3) reduction, i.e. the preparation of S-(-)-indoline-2-carboxylic acid
Add 75g tetrahydrofuran (THF) and 8.5g (0.37mol) sodium sand in the 500ml there-necked flask, add the new trimethyl carbinol 27.5g that steams under the violent stirring.At this moment, Dropwise 5 0g is dissolved with the tetrahydrofuran solution of 24.5g (0.125mol) S-indoline-6-chloro-2-carboxylic acid, back flow reaction 2 hours in 30 minutes.Reaction finishes after-filtration and removes unreacted sodium, remove behind the solvent product S-(-)-indoline-2-carboxylic acid, drying, the 12g product, 184～186 ℃ of fusing points,
(c=1.0, DMSO), yield 58.5%.
At last, it is also to be noted that what more than enumerate only is several specific embodiments of the present invention.Obviously, the invention is not restricted to above embodiment, many distortion can also be arranged.All distortion that those of ordinary skill in the art can directly derive or associate from content disclosed by the invention all should be thought protection scope of the present invention.
Claims (9)
1. the synthetic method of a S-(-)-indoline-2-carboxylic acid, it is characterized in that: with the L-phenylalanine is main starting raw material, may further comprise the steps successively:
1), chlorination: with L-phenylalanine, solvent and ethanol under agitation condition, feed chlorine and carry out chlorination reaction, the weight ratio of described L-phenylalanine and solvent is 1: 7～1: 12, described consumption of ethanol is 10%～31% of a L-phenylalanine amount of substance, temperature of reaction is 10～30 ℃, and the reaction times is 0.5～2 hour; With the hydrochloride crystal of described chlorination reaction gained be hydrolyzed successively, vacuum removal solvent, washing, drying step, L-2,4-dichlorobenzene L-Ala;
2), cyclization: with above-mentioned L-2,4-dichlorobenzene L-Ala carries out ring-closure reaction in solvent, under the effect of copper salt catalyst, described L-2, and the weight ratio of 4-dichlorobenzene L-Ala and solvent is 1: 1～1: 3, the weight of described copper salt catalyst is L-2,5%～15% of 4-dichlorobenzene L-Ala; Described temperature of reaction is 100～140 ℃, 2～6 hours reaction times; After reaction finishes, extract successively again, wash, dry, remove solvent step, S-indoline-6-chloro-2-carboxylic acid;
3), reduction: above-mentioned S-indoline-6-chloro-2-carboxylic acid and sodium, the trimethyl carbinol are carried out back flow reaction in solvent, the weight ratio of described S-indoline-6-chloro-2-carboxylic acid and solvent is 1: 4～1: 8.2, and the consumption of the sodium and the trimethyl carbinol is 1～3 times of amount of substance of S-indoline-6-chloro-2-carboxylic acid; Solvent step is filtered, removed to reaction after finishing again successively.
2. the synthetic method of S-according to claim 1 (-)-indoline-2-carboxylic acid, it is characterized in that: earlier S-indoline-6-chloro-2-carboxylic acid is mixed with partial solvent in the reduction reaction of described step 3), be made into concentration and be S-indoline-6-chloro-2-carboxylic acid solution of 49%, described S-indoline-6-chloro-2-carboxylic acid solution is added in the mixture that sodium, the trimethyl carbinol, residual solvent forms in the mode that drips carry out back flow reaction again.
3. the synthetic method of S-according to claim 1 and 2 (-)-indoline-2-carboxylic acid is characterized in that: the reflux time of described step 3) is 2～6 hours.
4. the synthetic method of S-according to claim 3 (-)-indoline-2-carboxylic acid is characterized in that: be hydrolyzed with frozen water in the hydrolysing step of described step 1).
5. the synthetic method of S-according to claim 4 (-)-indoline-2-carboxylic acid is characterized in that: solvent for use is a halides in the chlorination reaction of described step 1).
6. the synthetic method of S-according to claim 5 (-)-indoline-2-carboxylic acid is characterized in that: described halides is chloroform or tetracol phenixin.
7. the synthetic method of S-according to claim 6 (-)-indoline-2-carboxylic acid is characterized in that: used copper salt catalyst is cupric chloride or cuprous chloride in the ring-closure reaction described step 2).
8. the synthetic method of S-according to claim 7 (-)-indoline-2-carboxylic acid is characterized in that: solvent for use is a diethanolamine in the ring-closure reaction described step 2).
9. the synthetic method of S-according to claim 8 (-)-indoline-2-carboxylic acid is characterized in that: solvent for use is a tetrahydrofuran (THF) in the reduction reaction of described step 3).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100498874A CN100391945C (en) | 2005-05-31 | 2005-05-31 | S-(-)-indolyl-2-carboxylic acid synthesizing method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100498874A CN100391945C (en) | 2005-05-31 | 2005-05-31 | S-(-)-indolyl-2-carboxylic acid synthesizing method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1709871A CN1709871A (en) | 2005-12-21 |
| CN100391945C true CN100391945C (en) | 2008-06-04 |
Family
ID=35706166
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2005100498874A Expired - Fee Related CN100391945C (en) | 2005-05-31 | 2005-05-31 | S-(-)-indolyl-2-carboxylic acid synthesizing method |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100391945C (en) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CZ2006427A3 (en) | 2003-12-29 | 2006-11-15 | Sepracor Inc. | Pyrrole and pyrazole DAAO inhibitors |
| CN101553217A (en) | 2005-07-06 | 2009-10-07 | 塞普拉科公司 | Combinations of eszopiclone and trans 4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-n-methyl-1-napthalenamine or trans 4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-napthalenamine, and methods of treatment |
| CA2636275C (en) | 2006-01-06 | 2013-02-12 | Sepracor Inc. | Tetralone-based monoamine reuptake inhibitors |
| BRPI0706365A2 (en) | 2006-01-06 | 2011-03-22 | Sepracor Inc | CYCLEalkylamines as monoamine reuptake inhibitors |
| PT2013835E (en) | 2006-03-31 | 2016-01-06 | Sunovion Pharmaceuticals Inc | Preparation of chiral amides and amines |
| US7884124B2 (en) | 2006-06-30 | 2011-02-08 | Sepracor Inc. | Fluoro-substituted inhibitors of D-amino acid oxidase |
| US7902252B2 (en) | 2007-01-18 | 2011-03-08 | Sepracor, Inc. | Inhibitors of D-amino acid oxidase |
| BRPI0811639A2 (en) | 2007-05-31 | 2014-09-30 | Sepracor Inc | FENY CYCLOAKILAMINES REPLACED AS MONOAMINE RECAPTATION INHIBITORS |
| CN102060745A (en) * | 2010-11-23 | 2011-05-18 | 安徽世华化工有限公司 | Preparation method of (S)-indoline-2-carboxylic acid |
| CN108976161A (en) * | 2018-10-29 | 2018-12-11 | 雅本化学股份有限公司 | A kind of preparation method of S- indoline-2-carboxylic acid |
| CA3183877A1 (en) | 2020-06-23 | 2021-12-30 | Jean-Francois Briere | Process for the preparation of ortho-halogenated phenylalanine compounds |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5463077A (en) * | 1992-04-10 | 1995-10-31 | Rhone-Poulenc Rorer S.A. | Perhydroisoindole derivatives and preparation |
| JP2001294573A (en) * | 2000-04-13 | 2001-10-23 | Sumitomo Chem Co Ltd | Method for producing optically active indoline derivative |
| EP1323729A1 (en) * | 2003-03-12 | 2003-07-02 | Les Laboratoires Servier | Method for synthesis of (2S,3aS,7aS)-perhydroindole-2-carboxylic acid and esters thereof derivatives; and use in the synthesis of perindopril |
| EP1338591A1 (en) * | 2003-02-28 | 2003-08-27 | Les Laboratoires Servier | Method for synthesis of (2S,3aS,7aS)-perhydroindole-2- carboxylic acid and esters thereof, and use in the synthesis of perindopril |
| EP1348684A1 (en) * | 2003-04-09 | 2003-10-01 | Les Laboratoires Servier | Method for synthesis of (2S)-indoline-2-carboxylic acid; and use in the synthesis of perindopril |
| EP1354875A1 (en) * | 2003-05-19 | 2003-10-22 | Les Laboratoires Servier | Method for synthesis of (2S,3aS,7aS)-perhydroindole-2-carboxylic acid and esters thereof; and use in the synthesis of perindopril |
| EP1354874A1 (en) * | 2003-04-15 | 2003-10-22 | Les Laboratoires Servier | Method for synthesis of (2S,3aS,7aS)-perhydroindole-2-carboxylic acid and esters thereof; and use in the synthesis of perindopril |
| EP1354876A1 (en) * | 2003-06-13 | 2003-10-22 | Les Laboratoires Servier | Method for synthesis of (2S,3aS,7aS)-perhydroindole-2-carboxylic acid and esters thereof; and use in the synthesis of perindopril |
-
2005
- 2005-05-31 CN CNB2005100498874A patent/CN100391945C/en not_active Expired - Fee Related
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5463077A (en) * | 1992-04-10 | 1995-10-31 | Rhone-Poulenc Rorer S.A. | Perhydroisoindole derivatives and preparation |
| JP2001294573A (en) * | 2000-04-13 | 2001-10-23 | Sumitomo Chem Co Ltd | Method for producing optically active indoline derivative |
| EP1338591A1 (en) * | 2003-02-28 | 2003-08-27 | Les Laboratoires Servier | Method for synthesis of (2S,3aS,7aS)-perhydroindole-2- carboxylic acid and esters thereof, and use in the synthesis of perindopril |
| EP1323729A1 (en) * | 2003-03-12 | 2003-07-02 | Les Laboratoires Servier | Method for synthesis of (2S,3aS,7aS)-perhydroindole-2-carboxylic acid and esters thereof derivatives; and use in the synthesis of perindopril |
| EP1348684A1 (en) * | 2003-04-09 | 2003-10-01 | Les Laboratoires Servier | Method for synthesis of (2S)-indoline-2-carboxylic acid; and use in the synthesis of perindopril |
| EP1354874A1 (en) * | 2003-04-15 | 2003-10-22 | Les Laboratoires Servier | Method for synthesis of (2S,3aS,7aS)-perhydroindole-2-carboxylic acid and esters thereof; and use in the synthesis of perindopril |
| EP1354875A1 (en) * | 2003-05-19 | 2003-10-22 | Les Laboratoires Servier | Method for synthesis of (2S,3aS,7aS)-perhydroindole-2-carboxylic acid and esters thereof; and use in the synthesis of perindopril |
| EP1354876A1 (en) * | 2003-06-13 | 2003-10-22 | Les Laboratoires Servier | Method for synthesis of (2S,3aS,7aS)-perhydroindole-2-carboxylic acid and esters thereof; and use in the synthesis of perindopril |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1709871A (en) | 2005-12-21 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN100391945C (en) | S-(-)-indolyl-2-carboxylic acid synthesizing method | |
| CN106748950A (en) | A kind of preparation method of Bu Waxitan and its intermediate | |
| CN113292535B (en) | Method for preparing apaluamide intermediate and apaluamide | |
| CN108017613B (en) | Method for preparing polyaryl substituted naphthalene derivative by ruthenium-catalyzed reaction of heterocyclic aromatic ketone and tolane | |
| CN104610161A (en) | Preparation method for telmisartan | |
| CN107312003A (en) | A kind of synthetic method for preparing the chlorine guanine of 2 amino of high-purity 6 | |
| CN114315759B (en) | Preparation method of 2-methyl-1- (4-morpholinophenyl) -2-morpholinyl-1-propanone | |
| CN104177388A (en) | Bridged bisamido rare-earth amide compounds, and preparation method and application thereof | |
| CN110872247A (en) | Xofluza sulfur-containing heterocyclic compound, intermediate thereof and preparation method | |
| CN104817550A (en) | Preparation method of rivaroxaban | |
| CN111233617A (en) | Synthesis method of 1-iodoalkyne compound | |
| CN101717359A (en) | Method for synthesizing indapamide | |
| CN110183445A (en) | The synthetic method of Moxifloxacin and its derivative | |
| CN107602452B (en) | Synthetic method of 3-acyl pyridine compound | |
| CN108997305A (en) | A kind of new compound 3- methyl -4,5- dichloro-thiophene -2- carboxylic acid and preparation method thereof | |
| CN105566336A (en) | Novel method for removing methyl impurity in preparation of asenapine | |
| CN105153013B (en) | The synthetic method of the ketone of 6 bromine isoindoline 1 | |
| CN110981832A (en) | Preparation method of roxatidine acetate hydrochloride | |
| CN106810546A (en) | A kind of umeclidinium compound | |
| CN102249962B (en) | Preparation method of 1,1-disulfur-1-olefin | |
| CN111747879B (en) | Large-process synthesis method of erexib | |
| CN103664960B (en) | Pu Na is for the preparation method of Buddhist nun | |
| CN108586340B (en) | Synthesis method of 3-acyl hydrogenated azepine compound | |
| CN110590641B (en) | Green preparation method of 3-hydroxyisoindole-1-ketone series compounds | |
| CN112939893A (en) | Synthesis method of 4- (4-aminophenyl) -3-morpholinone |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| ASS | Succession or assignment of patent right |
Owner name: GUIYANG BURST CHEMICAL INDUSTRY CO., LTD. Free format text: FORMER OWNER: ZHEJIANG UNIVERSITY Effective date: 20091113 |
|
| C41 | Transfer of patent application or patent right or utility model | ||
| TR01 | Transfer of patent right |
Effective date of registration: 20091113 Address after: No. 346 Baiyun North Road, Baiyun District, Guizhou, Guiyang Patentee after: Guiyang Best Chemical Co., Ltd. Address before: Hangzhou City, Zhejiang Province ancient jade road 20 Patentee before: Zhejiang University |
|
| C17 | Cessation of patent right | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20080604 Termination date: 20120531 |