MX170706B - Procedimiento para la preparacion de (-) -n"ciano-n-3- piridil -n'- 1, 2, 2-trimetilpropilguanidina - Google Patents
Procedimiento para la preparacion de (-) -n"ciano-n-3- piridil -n'- 1, 2, 2-trimetilpropilguanidinaInfo
- Publication number
- MX170706B MX170706B MX019348A MX1934890A MX170706B MX 170706 B MX170706 B MX 170706B MX 019348 A MX019348 A MX 019348A MX 1934890 A MX1934890 A MX 1934890A MX 170706 B MX170706 B MX 170706B
- Authority
- MX
- Mexico
- Prior art keywords
- procedure
- preparation
- trimetilpropilguanidina
- piridil
- ciano
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C279/00—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
- C07C279/04—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of guanidine groups bound to acyclic carbon atoms of a carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Cardiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Epidemiology (AREA)
- Pyridine Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
La presente invención se refiere a un procedimiento para la preparación de (-) N"-ciano-N-3-piridil-N'-1,2,2-trimetilpropilguanidina o una sal de adición de ácido farmaceuticamente aceptable de la misma, el procedimiento está caracterizado porque consiste en: a) la resolución de la N"-ciano-N-3-piridil-N'-1,2,2-trimetilpropilguanidina racemica o b) hacer reaccionar (-)-N-3-piridinil-N'-(1,2,2-trimetilpropil)tiourea con una carbodiimida reactiva y cianamida y c) opcionalmente convertir el producto resultante en una sal de adición de ácido farmaceuticamente aceptable del mismo. El uso descrito de los compuestos es como agentes antihipertensores.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US30671489A | 1989-02-03 | 1989-02-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
MX170706B true MX170706B (es) | 1993-09-08 |
Family
ID=23186533
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX019348A MX170706B (es) | 1989-02-03 | 1990-02-01 | Procedimiento para la preparacion de (-) -n"ciano-n-3- piridil -n'- 1, 2, 2-trimetilpropilguanidina |
Country Status (13)
Country | Link |
---|---|
EP (1) | EP0381504A3 (es) |
JP (1) | JP2823631B2 (es) |
KR (1) | KR100220989B1 (es) |
CN (1) | CN1043527C (es) |
AU (1) | AU623217B2 (es) |
CA (1) | CA2009074C (es) |
HU (1) | HU208959B (es) |
IE (1) | IE900391L (es) |
IL (1) | IL93252A0 (es) |
MX (1) | MX170706B (es) |
NZ (1) | NZ232336A (es) |
PT (1) | PT93033B (es) |
ZA (1) | ZA90772B (es) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ229828A (en) * | 1988-08-09 | 1992-03-26 | Squibb & Sons Inc | Aryl cyanoguanidine derivatives and pharmaceutical compositions |
US5371086A (en) * | 1991-03-15 | 1994-12-06 | The Green Cross Corporation | Aminopyridine compounds |
JPH05294935A (ja) * | 1991-03-15 | 1993-11-09 | Green Cross Corp:The | アミノピリジン系化合物 |
AU4530693A (en) * | 1992-08-13 | 1994-03-15 | Upjohn Company, The | Cyanoguanidines as potassium channel blockers |
ATE176905T1 (de) * | 1993-06-11 | 1999-03-15 | Upjohn Co | Pyrimidine-cyanoguanidine als kaliumkanalblocker |
AU7888798A (en) * | 1996-12-26 | 1998-07-31 | Kirin Beer Kabushiki Kaisha | Drugs for ameliorating ophthalmic circulatory disturbance |
FR2760838B1 (fr) * | 1997-03-13 | 1999-05-21 | Corning Inc | Circuit fluidique integre d'execution d'un processus de preparation ou d'analyse d'un echantillon de matiere fluide, son procede de fabrication et appareil d'exploitation de ce circuit |
US6645968B2 (en) * | 1999-08-03 | 2003-11-11 | Abbott Laboratories | Potassium channel openers |
DE60036476T2 (de) * | 1999-08-03 | 2008-06-12 | Abbott Laboratories, Abbott Park | Kalium kanalaktivatoren |
CN105580233B (zh) * | 2013-09-27 | 2018-05-29 | 三菱电机株式会社 | 功率转换装置 |
JP7437932B2 (ja) * | 2019-12-27 | 2024-02-26 | 三井化学株式会社 | 廃水処理方法 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1489879A (en) * | 1974-12-20 | 1977-10-26 | Leo Pharm Prod Ltd | N'-cyano-n'-3-pyridylguanidines |
FR2624699B1 (fr) * | 1987-12-18 | 1990-04-13 | Bernard Lyon I Universite Clau | Derives heterocycliques de n-carbamoyl-, n-thiocarbamoyl- ou n-amidino-glycine ou beta-alanine utiles comme agents edulcorants |
-
1990
- 1990-02-01 MX MX019348A patent/MX170706B/es unknown
- 1990-02-01 IL IL93252A patent/IL93252A0/xx not_active IP Right Cessation
- 1990-02-01 CA CA002009074A patent/CA2009074C/en not_active Expired - Fee Related
- 1990-02-01 KR KR1019900001152A patent/KR100220989B1/ko not_active IP Right Cessation
- 1990-02-01 EP EP19900301073 patent/EP0381504A3/en not_active Withdrawn
- 1990-02-01 AU AU48977/90A patent/AU623217B2/en not_active Ceased
- 1990-02-01 ZA ZA90772A patent/ZA90772B/xx unknown
- 1990-02-01 NZ NZ232336A patent/NZ232336A/en unknown
- 1990-02-01 HU HU90641A patent/HU208959B/hu not_active IP Right Cessation
- 1990-02-01 PT PT93033A patent/PT93033B/pt not_active IP Right Cessation
- 1990-02-02 IE IE900391A patent/IE900391L/xx unknown
- 1990-02-02 JP JP2025003A patent/JP2823631B2/ja not_active Expired - Lifetime
- 1990-02-02 CN CN90100487A patent/CN1043527C/zh not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
IE900391L (en) | 1990-08-03 |
PT93033B (pt) | 1996-03-29 |
IL93252A0 (en) | 1990-11-29 |
CN1043527C (zh) | 1999-06-02 |
CA2009074A1 (en) | 1990-08-03 |
AU4897790A (en) | 1990-08-09 |
AU623217B2 (en) | 1992-05-07 |
HU900641D0 (en) | 1990-04-28 |
HU208959B (en) | 1994-02-28 |
CA2009074C (en) | 1999-07-27 |
ZA90772B (en) | 1991-10-30 |
JPH02235868A (ja) | 1990-09-18 |
CN1044654A (zh) | 1990-08-15 |
NZ232336A (en) | 1991-07-26 |
PT93033A (pt) | 1990-11-07 |
EP0381504A3 (en) | 1991-09-04 |
JP2823631B2 (ja) | 1998-11-11 |
KR100220989B1 (ko) | 1999-09-15 |
EP0381504A2 (en) | 1990-08-08 |
KR900012897A (ko) | 1990-09-03 |
HUT53876A (en) | 1990-12-28 |
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