KR830010065A - Manufacturing method of therapeutic agent - Google Patents

Manufacturing method of therapeutic agent Download PDF

Info

Publication number
KR830010065A
KR830010065A KR1019820001506A KR820001506A KR830010065A KR 830010065 A KR830010065 A KR 830010065A KR 1019820001506 A KR1019820001506 A KR 1019820001506A KR 820001506 A KR820001506 A KR 820001506A KR 830010065 A KR830010065 A KR 830010065A
Authority
KR
South Korea
Prior art keywords
formula
compound
carbon atoms
group
general formula
Prior art date
Application number
KR1019820001506A
Other languages
Korean (ko)
Other versions
KR900000274B1 (en
Inventor
에드워드 제퍼리 제임스
코즈릭 안토닌
챨스 윌름셜스트 에릭
Original Assignee
데렉 노르만 에드먼슨
너 부츠 캄파니 피 엘시
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=26279045&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=KR830010065(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by 데렉 노르만 에드먼슨, 너 부츠 캄파니 피 엘시 filed Critical 데렉 노르만 에드먼슨
Publication of KR830010065A publication Critical patent/KR830010065A/en
Application granted granted Critical
Publication of KR900000274B1 publication Critical patent/KR900000274B1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/16Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/18Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
    • C07D295/182Radicals derived from carboxylic acids
    • C07D295/185Radicals derived from carboxylic acids from aliphatic carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C211/00Compounds containing amino groups bound to a carbon skeleton
    • C07C211/01Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
    • C07C211/02Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/26Psychostimulants, e.g. nicotine, cocaine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
    • C07C29/136Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
    • C07C29/147Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C33/00Unsaturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C33/40Halogenated unsaturated alcohols
    • C07C33/50Halogenated unsaturated alcohols containing six-membered aromatic rings and other rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/004Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with organometalhalides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/42Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by hydrolysis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/44Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reduction and hydrolysis of nitriles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/20Unsaturated compounds containing keto groups bound to acyclic carbon atoms
    • C07C49/227Unsaturated compounds containing keto groups bound to acyclic carbon atoms containing halogen
    • C07C49/237Unsaturated compounds containing keto groups bound to acyclic carbon atoms containing halogen containing six-membered aromatic rings and other rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/527Unsaturated compounds containing keto groups bound to rings other than six-membered aromatic rings
    • C07C49/567Unsaturated compounds containing keto groups bound to rings other than six-membered aromatic rings containing halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C57/00Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
    • C07C57/46Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings and other rings, e.g. cyclohexylphenylacetic acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C61/00Compounds having carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings
    • C07C61/16Unsaturated compounds
    • C07C61/40Unsaturated compounds containing halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/06Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with radicals, containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/68Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D211/70Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/06Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by halogen atoms or nitro radicals
    • C07D295/073Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by halogen atoms or nitro radicals with the ring nitrogen atoms and the substituents separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Health & Medical Sciences (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Psychiatry (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Biomedical Technology (AREA)
  • Public Health (AREA)
  • Pain & Pain Management (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

내용 없음No content

Description

치료제의 제조방법Manufacturing method of therapeutic agent

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

Claims (13)

일반식(Ⅴ)의 케톤을 환원적 아미드화하여 n=0, R2=H, R4=CHO 인 일반식(Ⅰ)화합물을 제조하거나 일반식(Ⅵ)의 케톤 또는 알데히이드를 환원적 아미드화하여 n=1, R4=CHO, R8=H인 일반식(Ⅰ)화합물을 제조함을 특징으로 하여 일반식(Ⅰ)의 화합물 및 그의 약제학적으로 허용할 수 있는 염을 제조하는 방법.Reductive amidation of the ketone of formula (V) to prepare a compound of formula (I) wherein n = 0, R 2 = H, R 4 = CHO or reductively convert ketone or aldehyde of formula (VI) Amidation to prepare a compound of formula (I) wherein n = 1, R 4 = CHO, R 8 = H, to prepare a compound of formula (I) and pharmaceutically acceptable salts thereof Way. 상기식에서, n=0 또는 1이며, n=0일때, R1은 1내지 6개의 탄소원자를 함유하는 직쇄 또는 측쇄 알킬그룹, 3내지 7개의 탄소원자를 함유하는 사이클로알킬그룹, 사이클로알킬알킬그룹, (이때 사이클로알킬그룹은 3내지 6개의 탄소원자를 함유하며 알킬그룹은 1내지 3개의 탄소원자를 함유한다). 2내지 6개의 탄소원하를 함유하는 알케닐 또는 알키닐 그룹, 또는 다음 일반식(Ⅱ)의 그룹이며,Wherein n = 0 or 1 and when n = 0, R 1 is a straight or branched chain alkyl group containing 1 to 6 carbon atoms, a cycloalkyl group containing 3 to 7 carbon atoms, a cycloalkylalkyl group, ( Wherein the cycloalkyl group contains 3 to 6 carbon atoms and the alkyl group contains 1 to 3 carbon atoms). An alkenyl or alkynyl group containing 2 to 6 carbon atoms, or a group of the following general formula (II), 이때, R9와 R10은 같거나 다를 수 있으며 H, 할로 또는 1내지 3개의 탄소원자를 가지는 알콕시그룹이다.In this case, R 9 and R 10 may be the same or different and are H, halo or an alkoxy group having 1 to 3 carbon atoms. n=1일때, R1은 H 또는 1내지 3개의 탄소원자를 함유하는 알킬그룹이며, R2는 H 또는 1내지 3개의 탄소원자를 함유하는 알킬그룹이고, R3와 R4는 같거나 다를수 있으며, H, 1내지 4개의 탄소원자를 함유하는 알케닐그룹, 3내지 6개의 탄소원자를 가지는 알키닐그룹, 환이 3내지 7개의 탄소원자를 함유한 직쇄 또는 측쇄 알킬그룹, 3내지 6개의 탄소원자를 함유하는 사이클로알킬그룹, 일반식 R11CO그룹(이때 R11은 H이다)이거나, R3및 R4는 이들이 결합되어 있는 질소원자와 함께 환중에 5 또는 6개의 원자를 가지는 임의 치환된 헤테로사이클환을 형성하는데 이때 환은 질소원자 이외에 다른 헤테로원자를 함유할 수도 있으며; R5와 R6는 같거나 다를수 있으며, H, 할로, 트리플루오로메틸, 1내지 3개의 탄소원자를 가지는 알킬그룹, 1내지 3개의 탄소원자를 함유하는 알콕시 또는 알킬티오그룹, 페닐그룹이거나, R5및 R6는 이들이 결합된 탄소원자와 함께 하나이상의 할로그룹, 1내지 4개의 탄소원자를 함유하는 알킬 또는 알콕시그룹에 의해 임의 치환된 제2의 벤젠환을 형성하거나 제2벤젠환의 치환체는 이들이 결합되어 있는 2개의 탄소원자와 함께 또 다른 벤젠환을 형성할 수 있으며, R7과 R8은 같거나 다를수 있으며, H 또는 1내지 3개의 탄소원자를 함유하는 알킬그룹이다.when n = 1, R 1 is H or an alkyl group containing 1 to 3 carbon atoms, R 2 is H or an alkyl group containing 1 to 3 carbon atoms, and R 3 and R 4 may be the same or different, H, an alkenyl group containing 1 to 4 carbon atoms, an alkynyl group containing 3 to 6 carbon atoms, a straight or branched chain alkyl group containing 3 to 7 carbon atoms, cycloalkyl containing 3 to 6 carbon atoms Group, a general formula R 11 CO group wherein R 11 is H, or R 3 and R 4 together with the nitrogen atom to which they are attached form an optionally substituted heterocycle ring having 5 or 6 atoms in the ring; The ring may contain other heteroatoms in addition to the nitrogen atom; R 5 and R 6 may be the same or different, H, halo, trifluoromethyl, an alkyl group having 1 to 3 carbon atoms, an alkoxy or alkylthio group containing 1 to 3 carbon atoms, a phenyl group, or R 5 And R 6 together with the carbon atoms to which they are attached form a second benzene ring optionally substituted by one or more halo groups, alkyl or alkoxy groups containing 1 to 4 carbon atoms, or substituents of the second benzene ring to which they are attached Together with the two carbon atoms present, another benzene ring may be formed, and R 7 and R 8 may be the same or different and are H or an alkyl group containing 1 to 3 carbon atoms. 일반식(Ⅴ)의 케톤을 환원적 아민화하여 n=0, R2=H인 일반식(Ⅰ) 화합물을 제조하거나 일반식(Ⅵ)의 케톤 또는 알데하이드를 환원적 아민화하여 n=1, R8=H인 일반식(Ⅰ)화합물을 제조함을 특징으로 하여 일반식(Ⅰ)화합물을 제조하는 방법.Reductive amination of the ketone of formula (V) to prepare a compound of formula (I) wherein n = 0, R 2 = H or reductive amination of a ketone or aldehyde of formula (VI) to n = 1, A process for preparing a compound of formula (I), characterized in that to produce compound of formula (I) wherein R 8 = H. 상기식에서, n,R1,R2,R3,R4,R5,R6,R7및 R8은 제1항에서 정의된 바와 같다.Wherein n, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are as defined in claim 1. 일반식(Ⅶ)의 화합물을 환원시킴을 특징으로 하여 일반식(Ⅰ)의 화합물을 제조하는 방법.A method for preparing a compound of formula (I), characterized by reducing the compound of formula (VII). 상기식에서, n,R1,R2,R3,R4,R5,R6,R7및 R8은 제1항에서 정의된 바와 같고,Wherein n, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are as defined in claim 1, a) Z 가 일반식 -CR1=NOH그룹 또는)그외 에스테르 또는 에테르인 경우, n=0이고 R2,R3및 R4가 H인 일반식(Ⅰ)의 화합물이 수득되고,a) when Z is a general formula -CR 1 = NOH group or) or other esters or ethers, a compound of formula (I) is obtained wherein n = 0 and R 2 , R 3 and R 4 are H, b) Z 가 일반식 -CR1=NR3의 그룹인 경우, n=0이고 R2및 R4가 H인 일반식(Ⅰ)의 화합물이 수득되고b) when Z is a group of the formula -CR 1 = NR 3 , a compound of formula (I) is obtained in which n = 0 and R 2 and R 4 are H; c) Z 가 일반식 -CR1=NY의 그룹(Y는 유기금속 시약으로부터 유도된 금속함유 잔기를 나타낸다)인 경우, n=0이고 R2,R3및 R4가 H인 일반식(I)의 화합물이 수득되고c) when Z is a group of the formula -CR 1 = NY (Y represents a metal-containing moiety derived from an organometallic reagent), where n = 0 and R 2 , R 3 and R 4 are H (I ) Compound is obtained d) Z 가 일반식 -CR1R2CN의 그룹인 경우, n=1이고 R3,R4,R7및 R8이 H인 일반식(Ⅰ)의 화합물이 수득되고d) when Z is a group of the formula -CR 1 R 2 CN, a compound of formula (I) is obtained wherein n = 1 and R 3 , R 4 , R 7 and R 8 are H; e) Z 가 일반식 -CR1R2CR7=NOH 또는 그의 에스테르 또는 에테르인 경우, n=1이고, R2,R4및 R8이 H인 일반식(Ⅰ)의 화합물이 수득되고e) when Z is the formula -CR 1 R 2 CR 7 = NOH or its ester or ether, a compound of formula (I) is obtained in which n = 1 and R 2 , R 4 and R 8 are H; f) Z 가 일반식 -CR1R2CR7=NR3의 그룹인 경우 n=1이고, R4및 R8이 H인 일반식(Ⅰ)의 화합물이 수득되고f) when Z is a group of the formula -CR 1 R 2 CR 7 = NR 3 , a compound of formula (I) is obtained wherein n = 1 and R 4 and R 8 are H; g) Z 가 일반식 -CR1R2CR3CR7=NY(Y는 유기금속 시약으로부터 유도된 금속함유잔기를 나타낸다)의 그룹인 경우, n=1이고 R3,R4및 R8은 H인 일반식(Ⅰ)의 화합물이 수득된다.g) when Z is a group of the general formula —CR 1 R 2 CR 3 CR 7 = NY (Y represents a metal-containing residue derived from an organometallic reagent), n = 1 and R 3 , R 4 and R 8 are A compound of formula (I) is obtained, which is H. h) Z 가 일반식 -CR1R2CONR3R4의 그룹인 경우, n=1이고 R7및 R8은 H인 일반식(I)의 화합물이 수득된다.h) When Z is a group of the formula -CR 1 R 2 CONR 3 R 4 , a compound of formula (I) is obtained wherein n = 1 and R 7 and R 8 are H. 제3항에 있어서, Y가 MgBr 또는 Li임이 특징인 방법.The method of claim 3, wherein Y is MgBr or Li. 유기금속 시약을 일반식(Ⅶ)의 이민과 반응시킨후 생성물을 가수분해 시킴을 특징으로하여 n이 O인 일반식(Ⅰ)화합물을 제조하는 방법.A method of preparing a compound of formula (I) wherein n is O, characterized by reacting an organometallic reagent with an imine of general formula and then hydrolyzing the product. 상기식에서, n,R1,R2,R3,R4,R5,R6,R7및 R8은 제1항에서 정의된 바와 같다.Wherein n, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are as defined in claim 1. 제5항에 있어서, 유기금속 시약이 일반식 R1MgBr인 그리나드 시약이거나 일반식 R1Li인 유기리튬 화합물임이 특징인 방법.The method of claim 5, wherein the organometallic reagent is a Grignard reagent of the general formula R 1 MgBr or an organolithium compound of the general formula R 1 Li. 유기금속 시약을 일반식(Ⅸ)의 이민과 반응시킨후 생성물을 가수분해시킴을 특징으로하여 n이 1인 일반식(Ⅰ)화합물을 제조하는 방법.A method of preparing a compound of formula (I), wherein n is 1, by reacting an organometallic reagent with an imine of general formula and then hydrolyzing the product. 상기식에서, n,R1,R2,R3,R4,R5,R6,R7및 R8은 제1항에서 정의된 바와 같다.Wherein n, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are as defined in claim 1. 제7항에 있어서, 유기 금속 시약이 일반식 R7MgBr인 그리나드 시약이거나 일반식 R7Li인 유기리튬 화합물임이 특징인 방법.8. The method of claim 7, wherein the organometallic reagent is a Grignard reagent of general formula R 7 MgBr or an organolithium compound of general formula R 7 Li. 일반식(Ⅹ)의 아미드를 탈카복실화적으로 전위시켜 n=0인 일반식(Ⅰ)의 아민을 제조하거나, 일반식(XI)의 아미드를 탈카복실화 적으로 전위시켜 n=1인 일반식(Ⅰ)의 아민을 제조하거나, 나트륨 이자이드를 일반식(XⅡ)의 산 클로라이드와 반응시켜 생성된 아실아자이드를 탈카복실화적으로 전위시켜 n=0인 일반식(Ⅰ)의 아민을 제조하거나, 나트륨 이자이드를 일반식(XⅢ)의 산 클로라이드와 반응시켜 생성된 아실 아자이드를 탈카복실화적으로 전위시켜 n=1인 일반식(Ⅰ)의 아민을 제조함을 특징으로하여 일반식(Ⅰ)의 화합물을 제조하는 방법.The amide of general formula (VII) is decarboxylated to prepare an amine of general formula (I) having n = 0, or the amide of general formula (XI) is decarboxylated to general formula of n = 1. Preparing an amine of formula (I), or reacting sodium iside with an acid chloride of formula (XII) to decarboxylate the resulting acyl azide to prepare an amine of formula (I) with n = 0; , By reacting sodium iside with acid chloride of general formula (XIII) to decarboxylating the resulting acyl azide to produce an amine of general formula (I) with n = 1. To prepare a compound. 상기식에서, n,R1,R2,R3,R4,R5,R6,R7및 R8은 제1항에서 정의된 바와 같다.Wherein n, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are as defined in claim 1. 하이드라조 산을 일반식(XⅣ)의 카복실산과 반응시켜 n=0인 일반식(Ⅰ)의 아민을 제조하거나, 하이드라조산을 일반식(XV)의 카복실산과 반응시켜 n=1인 일반식(Ⅰ)의 아민을 제조함을 특징으로 하여 일반식(Ⅰ)의 화합물을 제조하는 방법.Hydrazoic acid is reacted with a carboxylic acid of formula (XIV) to prepare an amine of formula (I) with n = 0, or hydrazonic acid is reacted with a carboxylic acid of formula (XV) with n = 1 A process for preparing a compound of formula (I), characterized by preparing an amine of I). 상기식에서, n,R1,R2,R3,R4,R5,R6,R7및 R8은 제1항에서 정의된 바와 같다.Wherein n, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are as defined in claim 1. R4가 -CHO인 일반식(Ⅰ)화합물을 가수분해 시킴을 특징으로 하여 R4가 수소인 일반식(Ⅰ)화합물을 제조하는 방법.A method for producing a compound of formula (I) wherein R 4 is hydrogen, characterized by hydrolysis of compound of formula (I) wherein R 4 is -CHO. 상기식에서, n,R1,R2,R3,R4,R5,R6,R7및 R8은 제1항에서 정의된 바와 같다.Wherein n, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are as defined in claim 1. R4가 -CHO인 일반식(Ⅰ)화합물을 환원시킴을 특징으로 하여 R4가 메틸인 일반식(Ⅰ)화합물을 제조하는 방법.A process for preparing the compound of formula (I) wherein R 4 is methyl, characterized in that the compound of formula (I) wherein R 4 is -CHO is reduced. 상기식에서, n,R1,R2,R3,R4,R5,R6,R7및 R8은 제1항에서 정의된 바와 같다.Wherein n, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are as defined in claim 1. R3및 R4중의 하나 또는 둘다다 수소인 일반식(Ⅰ)화합물을 목적하는 화합물로 전환시킴을 특징으로 하여 R3및 R4중의 하나 또는 둘다다 수소이외의 기인 일반식(Ⅰ)화합물을 제조하는 방법.R 3 and R 4 is one or both of the hydrogen in the general formula (Ⅰ) one or both are a group other than hydrogen in a by R 3 and R 4 characterized in Sikkim converted to the compound of interest of the compound formula (Ⅰ) compound How to manufacture. 상기식에서, n,R1,R2,R3,R4,R5,R6,R7및 R8은 제1항에서 정의된 바와 같다.Wherein n, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are as defined in claim 1. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR828201506A 1981-04-06 1982-04-06 Process for the preparation of 1-(1-arylcyclobutyl)alkylamines KR900000274B1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
GB81-10709 1981-04-06
GB8110709 1981-04-06
GB8110709 1981-04-06
GB8110710 1981-04-06
GB8110710 1981-04-06

Publications (2)

Publication Number Publication Date
KR830010065A true KR830010065A (en) 1983-12-26
KR900000274B1 KR900000274B1 (en) 1990-01-24

Family

ID=26279045

Family Applications (1)

Application Number Title Priority Date Filing Date
KR828201506A KR900000274B1 (en) 1981-04-06 1982-04-06 Process for the preparation of 1-(1-arylcyclobutyl)alkylamines

Country Status (40)

Country Link
KR (1) KR900000274B1 (en)
AT (1) AT382612B (en)
AU (1) AU545595B2 (en)
BG (2) BG40652A3 (en)
CA (1) CA1248955A (en)
CH (1) CH652117A5 (en)
CS (1) CS244672B2 (en)
CY (1) CY1408A (en)
DD (1) DD208348A5 (en)
DE (1) DE3212682A1 (en)
DK (1) DK161770C (en)
ES (5) ES8305678A1 (en)
FI (1) FI77223C (en)
FR (1) FR2504920B1 (en)
GB (1) GB2098602B (en)
GE (1) GEP19970661B (en)
GR (1) GR76697B (en)
HK (1) HK13888A (en)
HU (1) HU186582B (en)
IE (1) IE52768B1 (en)
IL (1) IL65257A0 (en)
IN (1) IN155773B (en)
IT (1) IT1235758B (en)
JO (1) JO1184B1 (en)
KE (1) KE3753A (en)
LU (1) LU84070A1 (en)
MY (1) MY8800048A (en)
NL (1) NL192201C (en)
NO (1) NO156785C (en)
NZ (1) NZ200178A (en)
PH (1) PH22762A (en)
PL (2) PL136242B1 (en)
PT (1) PT74580B (en)
RO (2) RO89436A2 (en)
SE (1) SE452611B (en)
SG (1) SG67287G (en)
SU (2) SU1482522A3 (en)
UA (2) UA7838A1 (en)
YU (2) YU44336B (en)
ZW (1) ZW4982A1 (en)

Families Citing this family (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IE56000B1 (en) * 1982-09-30 1991-03-13 Boots Co Plc 1-arylcyclobutylalkylamine compounds
IE56001B1 (en) * 1982-09-30 1991-03-13 Boots Co Plc 1-arylcyclobutylmethylamine compounds
GB8412480D0 (en) * 1984-05-16 1984-06-20 Elliott M Pesticides
DK58285D0 (en) * 1984-05-30 1985-02-08 Novo Industri As PEPTIDES AND MANUFACTURING AND USING THEREOF
GB8501192D0 (en) * 1985-01-17 1985-02-20 Boots Co Plc Therapeutic agents
US5157021A (en) * 1985-03-15 1992-10-20 Novo Nordisk A/S Insulin derivatives and pharmaceutical preparations containing these derivatives
DK119785D0 (en) * 1985-03-15 1985-03-15 Nordisk Gentofte INSULIN PREPARATION
GB2184122B (en) * 1985-12-17 1989-10-18 Boots Co Plc N,n-dimethyl-1-[1-(4-chlorophenyl)cyclobutyl]-3-methyl butylamine hydrochloride monohydrate
GB8531071D0 (en) * 1985-12-17 1986-01-29 Boots Co Plc Therapeutic compound
GB8704777D0 (en) * 1987-02-28 1987-04-01 Boots Co Plc Medical treatment
JP2675573B2 (en) * 1988-03-31 1997-11-12 科研製薬株式会社 Brain function improver
EP0647134A4 (en) * 1992-06-23 1997-07-30 Sepracor Inc Methods and compositions for treating depression and other disorders using optically pure (-) sibutramine.
GB9309749D0 (en) * 1993-05-12 1993-06-23 Boots Co Plc Therapeutic agents
US5459164A (en) * 1994-02-03 1995-10-17 Boots Pharmaceuticals, Inc. Medical treatment
DE19518988A1 (en) * 1995-05-29 1996-12-05 Basf Ag Use of aryl substituted cyclobutylalkylamines to treat obesity
GB9524681D0 (en) 1995-12-02 1996-01-31 Knoll Ag Chemical process
GB9619757D0 (en) * 1996-09-21 1996-11-06 Knoll Ag Chemical process
GB9619961D0 (en) * 1996-09-25 1996-11-13 Knoll Ag Medical treatment
GB9619962D0 (en) * 1996-09-25 1996-11-13 Knoll Ag Medical treatment
GB9727131D0 (en) 1997-12-24 1998-02-25 Knoll Ag Therapeutic agents
AU2007200334B8 (en) * 1998-08-24 2010-10-21 Sepracor, Inc. Methods of using and compositions comprising dopamine reuptake inhibitors
US6974838B2 (en) 1998-08-24 2005-12-13 Sepracor Inc. Methods of treating or preventing pain using sibutramine metabolites
US6339106B1 (en) 1999-08-11 2002-01-15 Sepracor, Inc. Methods and compositions for the treatment and prevention of sexual dysfunction
US6331571B1 (en) 1998-08-24 2001-12-18 Sepracor, Inc. Methods of treating and preventing attention deficit disorders
US6476078B2 (en) 1999-08-11 2002-11-05 Sepracor, Inc. Methods of using sibutramine metabolites in combination with a phosphodiesterase inhibitor to treat sexual dysfunction
BG65170B1 (en) * 1999-03-17 2007-05-31 Knoll Gmbh Use of n-substituted derivatives of 1-[1-(4-chlorophenyl)cyclobutyl]-3-methylbutyl amine for the production of a medicine for treating eating disorders
US6552087B1 (en) 1999-03-19 2003-04-22 Abbott Gmbh & Co. Kg Therapeutic agent comprising (+)-sibutramine
GB9915617D0 (en) 1999-07-05 1999-09-01 Knoll Ag Therapeutic agents
US6399826B1 (en) 1999-08-11 2002-06-04 Sepracor Inc. Salts of sibutramine metabolites, methods of making sibutramine metabolites and intermediates useful in the same, and methods of treating pain
WO2002036540A2 (en) * 2000-11-02 2002-05-10 Torrent Pharmaceuticals Ltd PROCESS FOR PREPARATION OF β-PHENETHYLAMINE DERIVATIVE
US6610887B2 (en) 2001-04-13 2003-08-26 Sepracor Inc. Methods of preparing didesmethylsibutramine and other sibutramine derivatives
KR100536750B1 (en) * 2002-10-05 2005-12-16 한미약품 주식회사 Pharmaceutical composition comprising crystalline hemihydrate of sibutramine methanesulfonate
FR2870537A1 (en) * 2004-05-19 2005-11-25 Servier Lab NOVEL PROCESS FOR SYNTHESIZING (1S) -4,5-DIMETHOXY-1- (METHYL AMINOMETHYL) BENZOCYCLOBUTANE AND ITS ADDITION SALTS AND APPLICATION TO THE SYNTHESIS OF IVABRADINE AND ITS ADDITION SALTS PHARMACEUTICALLY ACCEPTABLE ACID
KR100606533B1 (en) 2004-08-27 2006-08-01 한올제약주식회사 An improved synthetic method of sibutramine
KR100606534B1 (en) 2004-11-01 2006-08-01 한올제약주식회사 An improved synthetic method of sibutramine
KR100618176B1 (en) * 2004-12-02 2006-09-01 휴먼팜 주식회사 Sibutramine tartrate, its preparation process and phamaceutical composition comprising it
WO2006073292A1 (en) 2005-01-06 2006-07-13 Cj Corporation Inorganic acid salts of sibutramine
AU2007296074B2 (en) * 2006-09-15 2012-07-12 Reviva Pharmaceuticals, Inc. Synthesis, methods of using, and compositions of cycloalkylmethylamines
CN101555214B (en) * 2008-04-08 2012-07-11 北京嘉事联博医药科技有限公司 Phenylcyclobutylacylamide derivative as well as optical isomer, preparation method and application thereof
FR2935381B1 (en) * 2008-08-29 2010-12-17 Servier Lab NOVEL METHOD FOR THE RESOLUTION OF ENANTIOMERES OF (3,4-DIMETHOXY-BICYCLOO-4.2.0-OCTA-1,3,5-TRIEN-7-YL) NITRILE AND APPLICATION TO THE SYNTHESIS OF IVABRADINE
WO2010082216A2 (en) * 2008-12-08 2010-07-22 Matrix Laboratories Ltd Novel salts of sibutramine and their crystal forms
RS53827B1 (en) 2009-11-02 2015-06-30 Pfizer Inc. Dioxa-bicyclo[3.2.1]octane-2,3,4-triol derivatives
WO2012003501A2 (en) 2010-07-02 2012-01-05 Reviva Pharmaceuticals, Inc. Compositions, synthesis, and methods of using cycloalkylmethylamine derivatives
UA114807C2 (en) * 2011-12-30 2017-08-10 Ревіва Фармасьютікалс, Інк. Compositions, synthesis, and methods of using phenylcycloalkylmethylamine derivatives
FR2993561B1 (en) * 2012-07-17 2014-10-31 Servier Lab PROCESS FOR ENZYMATIC SYNTHESIS OF (7S) -1- (3,4-DIMETHOXY BICYCLO [4.2.0] OCTA-1,3,5-TRIENE 7-YL) N-METHYL METHANAMINE, AND APPLICATION TO THE SYNTHESIS OF THE IVABRADINE AND ITS SALTS

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1124485B (en) * 1960-02-12 1962-03-01 Hoechst Ag Process for the preparation of analeptically active phenylcycloalkylmethylamines
US3526656A (en) * 1967-05-25 1970-09-01 Parke Davis & Co (1-arylcyclobutyl)carbonyl carbamic acid derivatives

Also Published As

Publication number Publication date
YU6385A (en) 1985-08-31
CS245782A2 (en) 1985-08-15
NL8201347A (en) 1982-11-01
PL136242B1 (en) 1986-02-28
YU44253B (en) 1990-04-30
GR76697B (en) 1984-08-28
DK161770B (en) 1991-08-12
JO1184B1 (en) 1983-11-30
AU545595B2 (en) 1985-07-18
KE3753A (en) 1987-10-02
PH22762A (en) 1988-12-12
DD208348A5 (en) 1984-05-02
FI821197L (en) 1982-10-07
ES8406414A1 (en) 1984-08-01
FI77223C (en) 1989-02-10
HK13888A (en) 1988-02-26
BG40652A3 (en) 1986-01-15
NL192201B (en) 1996-11-01
DE3212682C2 (en) 1992-03-26
GEP19970661B (en) 1997-01-04
ES519029A0 (en) 1984-08-01
PT74580B (en) 1983-12-23
RO89436A2 (en) 1986-06-30
GB2098602B (en) 1984-08-22
SE8202166L (en) 1982-11-25
YU44336B (en) 1990-06-30
UA7589A1 (en) 1995-09-29
IL65257A0 (en) 1983-12-30
ES8403097A1 (en) 1984-03-01
IT1235758B (en) 1992-09-28
PL240079A1 (en) 1983-09-12
YU75082A (en) 1985-08-31
CY1408A (en) 1988-04-22
PL139120B1 (en) 1986-12-31
ATA132582A (en) 1986-08-15
UA7838A1 (en) 1995-12-26
AT382612B (en) 1987-03-25
DK161770C (en) 1992-02-10
FR2504920A1 (en) 1982-11-05
KR900000274B1 (en) 1990-01-24
BG40651A3 (en) 1986-01-15
NO821087L (en) 1982-10-07
RO84802B (en) 1984-10-30
ES519032A0 (en) 1984-03-01
AU8221382A (en) 1982-10-14
RO84802A (en) 1984-09-29
DK146482A (en) 1982-10-07
SG67287G (en) 1988-02-19
NZ200178A (en) 1985-07-31
IE52768B1 (en) 1988-02-17
SE452611B (en) 1987-12-07
IT8248157A0 (en) 1982-04-02
CA1248955A (en) 1989-01-17
CS244672B2 (en) 1986-08-14
ES511152A0 (en) 1983-04-16
IE820481L (en) 1982-10-06
NL192201C (en) 1997-03-04
FI77223B (en) 1988-10-31
ES519030A0 (en) 1984-08-01
PT74580A (en) 1982-04-01
NO156785B (en) 1987-08-17
LU84070A1 (en) 1983-06-07
FR2504920B1 (en) 1985-06-28
DE3212682A1 (en) 1982-10-21
ES8407002A1 (en) 1984-08-16
MY8800048A (en) 1988-12-31
GB2098602A (en) 1982-11-24
CH652117A5 (en) 1985-10-31
ES8406413A1 (en) 1984-08-01
FI821197A0 (en) 1982-04-05
NO156785C (en) 1987-11-25
SU1461372A3 (en) 1989-02-23
ES519031A0 (en) 1984-08-16
HU186582B (en) 1985-08-28
ES8305678A1 (en) 1983-04-16
PL235832A1 (en) 1983-09-12
ZW4982A1 (en) 1982-11-03
SU1482522A3 (en) 1989-05-23
IN155773B (en) 1985-03-09

Similar Documents

Publication Publication Date Title
KR830010065A (en) Manufacturing method of therapeutic agent
KR860001104A (en) Method for producing tetrahydrophthalimide
JPS5490195A (en) Novel benzodiazepine compound
HUP0002953A2 (en) Method for preparation of citalopram and intermediates used for them
KR840004425A (en) Method for preparing N-alkyl-noscopene
JPS55127384A (en) Novel chromone compound*its manufacture and drug composition containing it
FR2382440A1 (en) PROCESS FOR OBTAINING METALLIC PHENATES, ESPECIALLY CALCIUM PHENATES
GB861561A (en) N-substituted piperidines
KR850002480A (en) Process for preparing pyrazole-ring alkylated pyrazolo quinoline
KR840006225A (en) Method for preparing phenylcyclobutylmethylamine derivative
KR870003107A (en) Method for preparing chianthine derivative
KR850004959A (en) Process for preparing aryloxy-N- (aminoalkyl) -1-pyrrolidine and piperidine carbox amide and carbothio amide
KR880007490A (en) Substituted aminopropionamides, methods of preparation thereof, medicaments containing the same, uses thereof and intermediates produced during the preparation thereof
ATE99318T1 (en) 4-SUBSTITUTED ANTHRACYCLINONES AND ANTHRACYCLINE GLYCOSIDES AND PROCESS FOR THEIR PRODUCTION.
KR840006224A (en) Process for preparing phenyl cyclobutyl alkylamine
KR830007568A (en) Method for preparing N- [amino (or hydroxy) phenethyl] -1,2,3,4-tetrahydroisoquinoline
ES8105970A1 (en) Preparation of fluorinated methylaminoalkanoic acids, process intermediates and their preparation.
CA2093048A1 (en) Benzo¢b!thiophen-5-yl derivative and process for producing the same
ATE18208T1 (en) N-(4-HYDROXYPHENYL)ACETIC ACID ESTERS FROM 5BENZOYL-1-METHYLPYRROL-2-ACETIC ACID.
JPS5519281A (en) Manufacture of amino acid and ester
KR840001123A (en) Method for preparing fluorinated diaminoalkene derivatives
Ramasseul et al. A useful protecting group in the preparation of amino-nitroxides
KR950032074A (en) Method for preparing β-nitroenamine and its intermediates
HUP0104064A2 (en) Method and intermediates for producing bis(oxim)monoethers
KR910015530A (en) Phenylacetamide derivatives and preparation methods thereof