KR840009085A - 7-옥사바이시클로헵탄치환 프로스타그란딘 동족체 제조방법 - Google Patents

7-옥사바이시클로헵탄치환 프로스타그란딘 동족체 제조방법 Download PDF

Info

Publication number
KR840009085A
KR840009085A KR1019840001248A KR840001248A KR840009085A KR 840009085 A KR840009085 A KR 840009085A KR 1019840001248 A KR1019840001248 A KR 1019840001248A KR 840001248 A KR840001248 A KR 840001248A KR 840009085 A KR840009085 A KR 840009085A
Authority
KR
South Korea
Prior art keywords
compound
methyl
oxabicyclo
hept
process according
Prior art date
Application number
KR1019840001248A
Other languages
English (en)
Inventor
에드워드 홀(외 1) 스티븐
Original Assignee
죠오지 제이. 코에서
이이. 아르. 스퀴부 앤드 산즈 인코오포레이티드
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
Priority claimed from US06/474,913 external-priority patent/US4474803A/en
Application filed by 죠오지 제이. 코에서, 이이. 아르. 스퀴부 앤드 산즈 인코오포레이티드 filed Critical 죠오지 제이. 코에서
Publication of KR840009085A publication Critical patent/KR840009085A/ko

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C405/00Compounds containing a five-membered ring having two side-chains in ortho position to each other, and having oxygen atoms directly attached to the ring in ortho position to one of the side-chains, one side-chain containing, not directly attached to the ring, a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, and the other side-chain having oxygen atoms attached in gamma-position to the ring, e.g. prostaglandins ; Analogues or derivatives thereof
    • C07C405/0008Analogues having the carboxyl group in the side-chains replaced by other functional groups
    • C07C405/0025Analogues having the carboxyl group in the side-chains replaced by other functional groups containing keto groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D493/00Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/08Bridged systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

내용 없음

Description

7-옥사바이시클로헵탄치환 프로스타그란딘 동족체 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (26)

  1. 다음 일반식(Ⅱ)의 화합물을 R1-OH 또는 R1-SH 기토에테트화시키거나 티오에테르화시키는 것을 특징으로 하는 다음 일반식(Ⅰ)의 화합물 및 그 입체이성체들의 제조방법.
  2. 위의 일반식(Ⅰ)에서, A는 -CH=CH- 또는 -(CH2)2-이고, B는 산소 (-O-) 또는이며, m는 1-8이고, n는 1-4이며, R는 수소, 알킬, 알칼리금속 또는 트리스(히드록시메틸) 아미노메탄이고, R1은 알킬, 알케닐, 알키닐, 아릴, 아랄킬, 아랄케닐, 아랄키닐, 시클로알킬, 시클로알킬알케닐 또는 시클로알킬알키닐임.
  3. 제1항에 있어서, B가 -O-임을 특징으로 하는 제조방법.
  4. 제1항에 있어서, B가 -S-임을 특징으로 하는 제조방단
  5. 제1-3항에 있어서, A가 -CH=CH-임을 특징으로 하는 제조방법.
  6. 제1-3항에 있어서, R가 H임을 특징으로 하는 제조방법.
  7. 제1-3항에 있어서, n가 1임을 특징으로 하는 제조방법.
  8. 제1-3항에 있어서, n가 2임을 특징으로 하는 제조방법.
  9. 제1-3항에 있어서, n가 3또는 4임을 특징으로 하는 제조방법.
  10. 제1-3항에 있어서, A가 -CH=CH-이고, m가 2-4이며, m가 1 또는 2이고, R가 H이며 R1가 저급알킬 또는 시클로알킬임을 특징으로 하는 제조방법.
  11. 제1-3항에 있어서, A는 -CH=CH-이고, m가 3이며, n는 1이고, R는 H, CH3또는 C6H13이며 R1가 저급알킬임을 특징으로 하는 제조방법.
  12. 제1항에 있어서, 목적하는 화합물이〔1β,2α(5Z),3α,4β〕-7-〔3-〔(헥실옥시)메틸〕-7-옥사비이시클로〔2.2.1〕헵트-2-〕-5-헵테노산 또는 그의 헬실에스테트인 제조방법.
  13. 제1항에 있어서, 목적하는 화합물이〔1β,2α(5Z),3α,4β〕-7-〔3-〔2-(펜틸옥시)메틸〕-7-옥사비이시클로〔2.2.1〕헵트-2-〕-5-헵테노산인 제조방법.
  14. 제1항에 있어서, 목적하는 화합물이〔1β,2α(5Z),3α,4β〕-7-〔3-페닐프로폭시)메틸〕-7-옥사비이시클로〔2.2.1〕헵트-2-일〕-5-헵테노인 제조방법.
  15. 제1항에 있어서, 목적하는 화합물이〔1β,2α(5Z),3α,4β〕-7-〔3-(옥틸옥시)메틸〕-7-옥사비이시클로〔2.2.1〕헵트-2-일〕-5-헵테노산인 제조방법.
  16. 제1항에 있어서, 목적하는 화합물이〔1β,2α(5Z),3α,4β〕-7-〔3-〔(시클로헥실메톡시)메틸〕-7-옥사비이시클로〔2.2.1〕헵트-2-일〕-5-헵테노산인 제조방법.
  17. 제1항에 있어서, A가 -CH=CH-이고, m가 3이며, n가 1이고, n´가 1이며 R1가 저급알킬인 제조방법.
  18. 제1항에 있어서, A가 -CH=CH-이고, m가 3이며, n가 1이고, n´가 2이며 R1가 저급알킬인 제조방법.
  19. 제1항에 있어서, 목적하는 화합물이〔1β,2α(5Z),3α,4β〕-7-〔3-〔(헥실옥시)메틸〕-7-옥사비이시클로〔2.2.1〕헵트-2-일〕-5-헵테노산 또는 그의 메틸에스테트인 제조방법.
  20. 제1항에 있어서, 목적하는 화합물이〔1β,2α(5Z),3α,4β〕-7-〔3-〔(헥실술피닐)메틸〕-7-옥사비이시클로〔2.2.1〕헵트-2-일〕-5-헵테노산 또는 그의 메틸에스테트인 제조방법.
  21. 제1항에 있어서, 목적하는 화합물이〔1β,2α(5Z),3α,4β〕-7-〔3-〔(헥실술포닐)메틸〕-7-옥사비이시클로〔2.2.1〕헵트-2-일〕-7-오헵테노산 또는 그의 메틸에스테트인 제조방법.
  22. 제1항에 있어서, 목적하는 화합물이〔1β,2α(5Z),3α,4β〕-7-〔3-〔(시클로헥실메틸)티오)메틸〕-7-옥사비이시클로〔2.2.1〕헵트-2-일〕-5-헵테노산 또는 그의 헬실에스테트인 제조방법.
  23. 제1항에 있어서, 목적하는 화합물이〔1β,2α(5Z),3α,4β〕-7-〔3-〔〔(2-페닐에틸)티오)메틸〕-7-옥사비이시클로〔2.2.1〕헵트-2-〕-5-헵테노산 또는 그의 헬실에스테트인 제조방법.
  24. 제1항에 있어서, 목적하는 화합물이 〔1β,2α(5Z),3α,4β〕-7-〔〔(3-페닐프로필)티오)메틸〕-7-옥사비이시클로〔2.2.1〕헵트-2-일〕-5-헵테노산 또는 그의 메틸에스테트인 제조방법.
  25. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019840001248A 1983-03-14 1984-03-13 7-옥사바이시클로헵탄치환 프로스타그란딘 동족체 제조방법 KR840009085A (ko)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US06/474,913 US4474803A (en) 1983-03-14 1983-03-14 7-Oxabicycloheptane substituted thio prostaglandin analogs useful in treating platelet aggregation and bronchoconstriction
US474913 1983-03-14
US52332083A 1983-08-15 1983-08-15
US523320 1990-05-14

Publications (1)

Publication Number Publication Date
KR840009085A true KR840009085A (ko) 1984-12-24

Family

ID=27044617

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019840001248A KR840009085A (ko) 1983-03-14 1984-03-13 7-옥사바이시클로헵탄치환 프로스타그란딘 동족체 제조방법

Country Status (24)

Country Link
KR (1) KR840009085A (ko)
AT (1) AT383600B (ko)
AU (1) AU567919B2 (ko)
CA (1) CA1256887A (ko)
CH (1) CH658247A5 (ko)
DD (1) DD216932A5 (ko)
DE (1) DE3409124A1 (ko)
DK (1) DK155584A (ko)
ES (1) ES530548A0 (ko)
FI (1) FI841008A (ko)
FR (1) FR2542743B1 (ko)
GB (1) GB2136428B (ko)
GR (1) GR79881B (ko)
HU (1) HU190530B (ko)
IE (1) IE57027B1 (ko)
IL (1) IL71184A0 (ko)
IT (1) IT1173442B (ko)
LU (1) LU85249A1 (ko)
NL (1) NL8400797A (ko)
NO (1) NO840960L (ko)
NZ (1) NZ207361A (ko)
PL (1) PL246663A1 (ko)
PT (1) PT78242B (ko)
SE (1) SE8401398L (ko)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4513103A (en) * 1983-10-21 1985-04-23 E. R. Squibb & Sons, Inc. 7-Oxabicycloheptane ethers useful in the treatment of thrombolytic disease
US4526900A (en) * 1984-01-26 1985-07-02 E. R. Squibb & Sons, Inc. 7-Oxabicycloheptane substituted oxa prostaglandin analogs and their use in the treatment of thrombolytic disease
US4542157A (en) * 1984-04-27 1985-09-17 E. R. Squibb & Sons, Inc. 7-Oxabicycloheptane substituted oxa prostaglandin analogs and their use in the treatment of thrombolytic disease
US4560698A (en) * 1984-06-04 1985-12-24 E. R. Squibb & Sons, Inc. 7-Oxabicycloheptane substituted thio prostaglandin analogs and their use in the treatment in thrombolytic disease
US4661506A (en) * 1984-11-30 1987-04-28 E. R. Squibb & Sons, Inc. 7-oxabicycloheptane substituted ox prostaglandin analogs
US4588743A (en) * 1985-01-22 1986-05-13 E. R. Squibb & Sons, Inc. 7-oxabicycloheptane-substituted oxa prostaglandin analogs and their use in the treatment of thrombolytic disease
US4607049A (en) * 1985-04-22 1986-08-19 E. R. Squibb & Sons, Inc. 7-oxabicycloheptane substituted thio prostaglandin analogs useful in the treatment of thrombolytic disease
US4608386A (en) * 1985-04-26 1986-08-26 E. R. Squibb & Sons, Inc. 7-oxabicycloheptane ethers useful in the treatment of thrombotic diseases
US4611006A (en) * 1985-06-28 1986-09-09 E. R. Squibb & Sons, Inc. 5,6-epoxy-7-oxabicycloheptane substituted ethers useful in the treatment of thrombotic disease
US4654356A (en) * 1985-08-01 1987-03-31 E. R. Squibb & Sons, Inc. 7-oxabicycloheptane substituted diacid diamide prostaglandin analogs
US4673685A (en) * 1986-07-23 1987-06-16 E. R. Squibb & Sons, Inc. Hydroximic acids of 7-oxabicycloheptane substituted ethers and thioethers useful in the treatment of thrombotic disease

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4143054A (en) * 1977-11-04 1979-03-06 E. R. Squibb & Sons, Inc. 7-oxabicycloheptane- and 7-oxabicycloheptene compounds
ZA829068B (en) * 1980-07-01 1983-02-23 Nat Res Dev Prostaglandins
US4628061A (en) * 1981-12-23 1986-12-09 National Research Development Corporation Prostaglandins
US4549030A (en) * 1982-12-13 1985-10-22 The Upjohn Company Organic compounds and process
US4526900A (en) * 1984-01-26 1985-07-02 E. R. Squibb & Sons, Inc. 7-Oxabicycloheptane substituted oxa prostaglandin analogs and their use in the treatment of thrombolytic disease
US4542157A (en) * 1984-04-27 1985-09-17 E. R. Squibb & Sons, Inc. 7-Oxabicycloheptane substituted oxa prostaglandin analogs and their use in the treatment of thrombolytic disease

Also Published As

Publication number Publication date
FI841008A (fi) 1984-09-15
CA1256887A (en) 1989-07-04
AU567919B2 (en) 1987-12-10
GR79881B (ko) 1984-10-31
DK155584D0 (da) 1984-03-13
SE8401398L (sv) 1984-09-15
PL246663A1 (en) 1985-03-26
CH658247A5 (fr) 1986-10-31
IL71184A0 (en) 1984-06-29
LU85249A1 (fr) 1984-11-14
NL8400797A (nl) 1984-10-01
IE57027B1 (en) 1992-03-25
FI841008A0 (fi) 1984-03-13
DD216932A5 (de) 1985-01-02
HU190530B (en) 1986-09-29
DE3409124A1 (de) 1984-09-27
GB2136428A (en) 1984-09-19
FR2542743B1 (fr) 1987-10-30
SE8401398D0 (sv) 1984-03-13
IT8420049A0 (it) 1984-03-14
IT1173442B (it) 1987-06-24
FR2542743A1 (fr) 1984-09-21
NZ207361A (en) 1986-12-05
PT78242B (en) 1986-05-27
GB8406100D0 (en) 1984-04-11
AT383600B (de) 1987-07-27
ES8506270A1 (es) 1985-07-01
DK155584A (da) 1984-09-15
AU2523584A (en) 1984-09-20
IE840525L (en) 1984-09-14
GB2136428B (en) 1986-09-10
ES530548A0 (es) 1985-07-01
ATA83484A (de) 1986-12-15
PT78242A (en) 1984-04-01
NO840960L (no) 1984-09-17
HUT34179A (en) 1985-02-28

Similar Documents

Publication Publication Date Title
KR840009085A (ko) 7-옥사바이시클로헵탄치환 프로스타그란딘 동족체 제조방법
MA19843A1 (fr) Nouveaux derives de la thieno ( 3,2-c ) pyridine, leur procede de preparation et leur application therapeutique .
SE8008524L (sv) 4-pregnen-derivat, ett forfarande for deras framstellning, beredning och metod for behandling av inflammatoriska tillstand
CA1257286A (en) 7-oxabicycloheptane substituted thio prostaglandin analogs
JPS56142262A (en) Piperazine derivative
ES2077083T3 (es) Procedimiento para la flotacion selectiva de menas de metal utilizando derivados de mercaptotiazol.
KR830006287A (ko) 아데닌 뉴클레오시드 유도체의 제조방법
KR830010039A (ko) 페닐 지방성 카복실린산 유도체의 제조방법
KR830007626A (ko) 2-(1,4-벤조디옥산-2-일알킬) 이미다졸류의 제조방법
PL249964A1 (en) Process for preparing novel derivatives of 7-//z/-2-/2-aminothiazolyl-4/-2-oxyiminoacetamide/-3-cephemo-4-carboxylic acid
KR870001212A (ko) 피리딘 유도체의 제조방법
EP0183238A3 (en) 7-oxabicycloheptane substituted oxa prostaglandin analogs
US4542157A (en) 7-Oxabicycloheptane substituted oxa prostaglandin analogs and their use in the treatment of thrombolytic disease
KR890003786A (ko) 신규의 불포화 아미노산 화합물의 제조방법
GR3005135T3 (ko)
EP0164075B1 (en) 7-oxabicycloheptane substituted thio prostaglandin analogs
US4082783A (en) 2A,2B-Dihomo-15-alkyl PGF1 α analogs
KR860004030A (ko) 브로모디클로로 이미다졸 살충제의 제조방법
US4311834A (en) 2-Decarboxy-2-tetrazolyl-19-hydroxy-19-methyl-6-oxo-PGF1 compounds
US4259529A (en) 2-Decarboxy-2-hydroxymethyl-19,20-didehydro-13,14-dihydro-PG1 compounds
US4257980A (en) 2-Decarboxy-2-aminomethyl-19,20-didehydro-13,14-dihydro-PG1 compounds
KR860009015A (ko) 이소퀴놀린 화합물의 제조방법
JPS5236646A (en) Process for preparation of prostaglandin derivatives and pharmceutical composition containing the compounds as effectual components
US4255354A (en) 2-Decarboxy-2-aminomethyl-19-hydroxy-19-methyl-6-oxo-PGF1 compounds
KR870003114A (ko) 테트라하이드로이소퀴놀린 유도체

Legal Events

Date Code Title Description
WITN Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid