LV12824B - Process for preparing new fibrinogen receptor antagonists - Google Patents

Process for preparing new fibrinogen receptor antagonists

Info

Publication number
LV12824B
LV12824B LVP-02-41A LV020041A LV12824B LV 12824 B LV12824 B LV 12824B LV 020041 A LV020041 A LV 020041A LV 12824 B LV12824 B LV 12824B
Authority
LV
Latvia
Prior art keywords
receptor antagonists
fibrinogen receptor
preparing new
new fibrinogen
10alkyl
Prior art date
Application number
LVP-02-41A
Other languages
English (en)
Latvian (lv)
Other versions
LV12824A (en
Inventor
John Y.L. Chung
David L. HUGHES
Dalian Zhao
Original Assignee
Merck & Co. Inc.
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
Application filed by Merck & Co. Inc. filed Critical Merck & Co. Inc.
Publication of LV12824A publication Critical patent/LV12824A/en
Publication of LV12824B publication Critical patent/LV12824B/xx

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/24Heterocyclic 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 substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/28Radicals substituted by singly-bound oxygen or sulphur atoms
    • C07D213/30Oxygen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/01Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
    • C07C311/02Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C311/03Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C311/06Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms to acyclic carbon atoms of hydrocarbon radicals substituted by carboxyl groups
    • 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
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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
    • C07D211/08Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/18Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D211/20Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms
    • C07D211/22Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms by oxygen atoms
LVP-02-41A 1992-02-28 2002-03-15 Process for preparing new fibrinogen receptor antagonists LV12824B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US07/843,658 US5206373A (en) 1992-02-28 1992-02-28 Process for preparing fibrinogen receptor antagonists

Publications (2)

Publication Number Publication Date
LV12824A LV12824A (en) 2002-05-20
LV12824B true LV12824B (en) 2002-09-20

Family

ID=25290632

Family Applications (1)

Application Number Title Priority Date Filing Date
LVP-02-41A LV12824B (en) 1992-02-28 2002-03-15 Process for preparing new fibrinogen receptor antagonists

Country Status (25)

Country Link
US (1) US5206373A (cs)
EP (2) EP0558139B1 (cs)
JP (1) JP2674679B2 (cs)
KR (1) KR100187779B1 (cs)
CN (1) CN1050832C (cs)
AR (1) AR247878A1 (cs)
AT (1) ATE156118T1 (cs)
AU (2) AU3732293A (cs)
CA (1) CA2090509C (cs)
CZ (1) CZ283485B6 (cs)
DE (1) DE69312528T2 (cs)
DK (1) DK0558139T3 (cs)
ES (2) ES2156255T3 (cs)
FI (1) FI106023B (cs)
GR (2) GR3024965T3 (cs)
HU (2) HU217959B (cs)
LV (1) LV12824B (cs)
MX (1) MX9301045A (cs)
NZ (1) NZ249751A (cs)
RO (1) RO116016B1 (cs)
RU (2) RU2097377C1 (cs)
SK (1) SK281250B6 (cs)
TW (1) TW229206B (cs)
WO (1) WO1993016995A1 (cs)
YU (1) YU49077B (cs)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1264813B1 (it) * 1993-07-28 1996-10-10 Oxon Italia Spa Procedimento per la preparazione di alcansolfonammidi
US5780480A (en) * 1996-02-28 1998-07-14 Merck & Co., Inc. Fibrinogen receptor antagonists
US5980951A (en) * 1996-04-10 1999-11-09 Merck & Co., Inc. Oral coated active drugs
WO1998000137A1 (en) 1996-07-01 1998-01-08 Eli Lilly And Company Hypoglycemic and hypolipidemic compounds
GB9812088D0 (en) * 1998-06-05 1998-08-05 Celltech Therapeutics Ltd Chemical compounds
CN1330636C (zh) * 2005-09-26 2007-08-08 鲁南制药集团股份有限公司 盐酸替罗非班中间体的合成方法
CN102452975A (zh) * 2010-11-01 2012-05-16 天津康鸿医药科技发展有限公司 盐酸替罗非班中间体合成方法
CN104447509B (zh) * 2013-09-18 2016-08-24 嘉实(湖南)医药科技有限公司 一种盐酸替罗非班的制备工艺
CN108440393A (zh) * 2018-03-20 2018-08-24 成都倍特药业有限公司 替罗非班物料杂质、杂质制备及物料中杂质检测方法
CN109608387A (zh) * 2019-01-02 2019-04-12 海门慧聚药业有限公司 盐酸替罗非班的制备
CN111100066B (zh) * 2019-11-29 2021-07-30 石药集团恩必普药业有限公司 一种盐酸替罗非班中间体及盐酸替罗非班的制备方法
CN112816282B (zh) * 2020-12-29 2022-04-12 江苏慧聚药业股份有限公司 一种盐酸替罗非班的有关物质及其制备和检测方法
CN115181058A (zh) * 2021-04-01 2022-10-14 武汉武药科技有限公司 组合物及其质量控制方法
CN114315697A (zh) * 2021-12-20 2022-04-12 河北国龙制药有限公司 一种盐酸替罗非班的制备方法

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB756713A (en) * 1953-07-06 1956-09-05 Ciba Ltd Substituted piperidines and process of making them
GB772516A (en) * 1953-12-22 1957-04-17 Ciba Ltd Piperidines and process of making same
GB939019A (en) * 1959-01-19 1963-10-09 Aspro Nicholas Ltd Diphenyl methane derivatives and methods for the preparation thereof
IT1062206B (it) * 1974-02-01 1983-09-20 Rotta Research Lab S P A A S Derivati della tirosina attivi sulla muscolatura liscia
DE2809377A1 (de) * 1978-03-04 1979-09-13 Boehringer Mannheim Gmbh Phenoxyalkylcarbonsaeure-derivate, verfahren zu deren herstellung sowie diese verbindungen enthaltende arzneimittel
US5084466A (en) * 1989-01-31 1992-01-28 Hoffmann-La Roche Inc. Novel carboxamide pyridine compounds which have useful pharmaceutical utility
CA2008116C (en) * 1989-02-23 2001-11-20 Thomas Weller Glycine derivatives
IL99537A (en) * 1990-09-27 1995-11-27 Merck & Co Inc Fibrinogen receptor antagonists and pharmaceutical preparations containing them
NZ239846A (en) * 1990-09-27 1994-11-25 Merck & Co Inc Sulphonamide derivatives and pharmaceutical compositions thereof

Also Published As

Publication number Publication date
RO116016B1 (ro) 2000-09-29
JP2674679B2 (ja) 1997-11-12
TW229206B (cs) 1994-09-01
FI106023B (fi) 2000-11-15
HU9402467D0 (en) 1994-10-28
EP0738714B1 (en) 2001-05-02
GR3024965T3 (en) 1998-01-30
CN1076441A (zh) 1993-09-22
AU3383693A (en) 1993-09-02
ES2105069T3 (es) 1997-10-16
DK0558139T3 (da) 1997-09-01
US5206373A (en) 1993-04-27
CA2090509A1 (en) 1993-08-29
YU13193A (sh) 1997-07-31
YU49077B (sh) 2003-08-29
HU226957B1 (en) 2010-03-29
JPH069557A (ja) 1994-01-18
FI943933A0 (fi) 1994-08-26
AU3732293A (en) 1993-09-13
ATE156118T1 (de) 1997-08-15
NZ249751A (en) 1996-06-25
RU94040166A (ru) 1996-07-10
CZ283485B6 (cs) 1998-04-15
AR247878A1 (es) 1995-04-28
HU217959B (hu) 2000-05-28
MX9301045A (es) 1993-09-01
HUT70537A (en) 1995-10-30
HU9600658D0 (en) 1996-05-28
EP0738714A3 (en) 1996-11-20
RU2097377C1 (ru) 1997-11-27
CN1050832C (zh) 2000-03-29
WO1993016995A1 (en) 1993-09-02
CZ203394A3 (en) 1995-10-18
SK102294A3 (en) 1995-04-12
EP0558139B1 (en) 1997-07-30
KR950700252A (ko) 1995-01-16
DE69312528T2 (de) 1998-02-19
DE69312528D1 (de) 1997-09-04
LV12824A (en) 2002-05-20
GR3035827T3 (en) 2001-08-31
SK281250B6 (sk) 2001-01-18
KR100187779B1 (ko) 1999-06-01
CA2090509C (en) 1997-02-25
EP0558139A1 (en) 1993-09-01
ES2156255T3 (es) 2001-06-16
FI943933A (fi) 1994-10-04
EP0738714A2 (en) 1996-10-23
AU657199B2 (en) 1995-03-02
RU2114105C1 (ru) 1998-06-27

Similar Documents

Publication Publication Date Title
LV12824B (en) Process for preparing new fibrinogen receptor antagonists
CA2324959A1 (en) Phthalimido compounds as intermediates for producing substance p receptor antagonists
HU908122D0 (en) Process for producing nitrogen containing spirocycles
GR1002697B (el) ΣΥΝΘΕΣΙΣ 3-[4-(2-ΑΜΙΝΟΑΙΘΟΞΥ)-ΒΕΝΖΟΥΛΟ]-2-ΑΡΥΛΟ-6-ΥΔΡΟΞΥΒΕΝΖΟ[b]ΘΕΙΟΦΑΙΝΙΩΝ.
MY108967A (en) Triazolopyridazine compounds, their production and use
NZ219228A (en) Production of organic compounds from synthesis gas
EP0665208A4 (cs)
DK1034174T3 (da) Azaringetherderivater og disses anvendelse som nikotin-ACh-receptormodulatorer
NO894349L (no) Tienopyridin-type mevalonolaktoner.
HUT38648A (en) Process for producing beta-lactam antibiotica and pharmaceutical, growth-controlling and antioxidative compositions
UA72883C2 (uk) Біциклічна сполука, способи її одержання, фармацевтичні композиції, що її містять,способи лікування та попередження різних захворювань, проміжні сполуки та способи їх одержання
AP9801410A0 (en) Indoline derivatives useful as 5-HT-2C receptor antagonists.
GR3014992T3 (en) Oxysulfonyl carbamates.
ES451067A1 (es) Un procedimiento de preparacion de derivados de fenotiazina.
DE3175327D1 (en) Antihypertensive lactams
ES502064A0 (es) Procedimiento de producir amidas ciclicas
ES8104296A1 (es) Procedimiento para preparar derivados de morfonas y normor- fonas
ES480969A1 (es) Procedimiento para la aclaracion optica de materiales organicos, en especial de tipo textil.
NZ332245A (en) Substituted benzo-oxazolol carboxylic acid derivatives, process for their production and medicaments containing them
IL111989A (en) 3-substituted 1-arylindole compounds and pharmaceutical compositions containing them
ES457696A1 (es) Un procedimiento mejorado para preparar un compuesto de prostaglandina opticamente activo.
ES8506700A1 (es) Un procedimiento para preparar nuevas 5-aminometil-imidazol-1-il-1,3-dialquil-1h-pirazol-4-il-aroil-metanonas
ES474786A1 (es) Procedimiento para la preparacion de nuevos compuestos hete-rociclicos