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JPS5262265A - Method - Google Patents

Method

Info

Publication number
JPS5262265A
JPS5262265A JP51134735A JP13473576A JPS5262265A JP S5262265 A JPS5262265 A JP S5262265A JP 51134735 A JP51134735 A JP 51134735A JP 13473576 A JP13473576 A JP 13473576A JP S5262265 A JPS5262265 A JP S5262265A
Authority
JP
Japan
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.)
Granted
Application number
JP51134735A
Other languages
English (en)
Other versions
JPS6228158B2 (ja
Inventor
Pauru Shiefuaado Kenesu
Henrii Ban Riinen Baaran
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pharmacia and Upjohn Co
Original Assignee
Upjohn Co
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 Upjohn Co filed Critical Upjohn Co
Publication of JPS5262265A publication Critical patent/JPS5262265A/ja
Publication of JPS6228158B2 publication Critical patent/JPS6228158B2/ja
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J31/00Normal steroids containing one or more sulfur atoms not belonging to a hetero ring
    • C07J31/003Normal steroids containing one or more sulfur atoms not belonging to a hetero ring the S atom directly linked to a ring carbon atom of the cyclopenta(a)hydrophenanthrene skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J1/00Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
    • C07J1/0003Androstane derivatives
    • C07J1/0011Androstane derivatives substituted in position 17 by a keto group
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J1/00Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
    • C07J1/0003Androstane derivatives
    • C07J1/0033Androstane derivatives substituted in position 17 alfa and 17 beta
    • C07J1/004Androstane derivatives substituted in position 17 alfa and 17 beta the substituent in position 17 alfa being an unsaturated hydrocarbon group
    • C07J1/0048Alkynyl derivatives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J5/00Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond
    • C07J5/0046Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond substituted in position 17 alfa
    • C07J5/0053Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond substituted in position 17 alfa not substituted in position 16
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J5/00Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond
    • C07J5/0046Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond substituted in position 17 alfa
    • C07J5/0061Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond substituted in position 17 alfa substituted in position 16
    • C07J5/0069Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond substituted in position 17 alfa substituted in position 16 by a saturated or unsaturated hydrocarbon group
    • C07J5/0076Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond substituted in position 17 alfa substituted in position 16 by a saturated or unsaturated hydrocarbon group by an alkyl group
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J7/00Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms
    • C07J7/0005Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21
    • C07J7/001Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21 substituted in position 20 by a keto group
    • C07J7/004Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21 substituted in position 20 by a keto group substituted in position 17 alfa
    • C07J7/0045Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21 substituted in position 20 by a keto group substituted in position 17 alfa not substituted in position 16
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J7/00Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms
    • C07J7/0005Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21
    • C07J7/0065Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21 substituted in position 20 by an OH group free esterified or etherified
    • C07J7/0075Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21 substituted in position 20 by an OH group free esterified or etherified substituted in position 17 alfa
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J7/00Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms
    • C07J7/008Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms substituted in position 21
    • C07J7/0085Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms substituted in position 21 by an halogen atom

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Steroid Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Electromechanical Clocks (AREA)
  • Electric Clocks (AREA)
JP51134735A 1975-11-17 1976-11-11 Method Granted JPS5262265A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US05/632,671 US4041055A (en) 1975-11-17 1975-11-17 Process for the preparation of 17α-hydroxyprogesterones and corticoids from androstenes

Publications (2)

Publication Number Publication Date
JPS5262265A true JPS5262265A (en) 1977-05-23
JPS6228158B2 JPS6228158B2 (ja) 1987-06-18

Family

ID=24536447

Family Applications (3)

Application Number Title Priority Date Filing Date
JP51134735A Granted JPS5262265A (en) 1975-11-17 1976-11-11 Method
JP61262903A Granted JPS6354391A (ja) 1975-11-17 1986-11-06 ステロイドの製法
JP61262901A Granted JPS6354393A (ja) 1975-11-17 1986-11-06 17α−ヒドロキシステロイド及びその製法

Family Applications After (2)

Application Number Title Priority Date Filing Date
JP61262903A Granted JPS6354391A (ja) 1975-11-17 1986-11-06 ステロイドの製法
JP61262901A Granted JPS6354393A (ja) 1975-11-17 1986-11-06 17α−ヒドロキシステロイド及びその製法

Country Status (12)

Country Link
US (1) US4041055A (ja)
JP (3) JPS5262265A (ja)
CH (2) CH636362A5 (ja)
DE (1) DE2649753C2 (ja)
FR (2) FR2351997A1 (ja)
GB (4) GB1531049A (ja)
HU (8) HU174396B (ja)
IE (1) IE44548B1 (ja)
IL (3) IL50787A (ja)
MX (1) MX4328E (ja)
NL (1) NL170420C (ja)
PL (3) PL116356B1 (ja)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6354391A (ja) * 1975-11-17 1988-03-08 ジ アツプジヨン カンパニ− ステロイドの製法

Families Citing this family (53)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4216159A (en) * 1978-05-25 1980-08-05 The Upjohn Company Synthesis of 16-unsaturated pregnanes from 17-keto steroids
US4336200A (en) * 1980-01-31 1982-06-22 The Upjohn Company 17α-Acyloxy-5β-corticoids
FR2486947A1 (fr) * 1980-07-15 1982-01-22 Roussel Uclaf Nouveaux derives steroides 20-isonitriles 17(20) insatures, leur procede de preparation et leur application a la preparation des steroides 17a-hydroxy 20-ceto
HU183397B (en) * 1981-04-16 1984-04-28 Richter Gedeon Vegyeszet Process for preparing 17alpha-hydroxy-pregn-4-ene-3,20-dione derivatives
US4342702A (en) * 1981-05-18 1982-08-03 The Upjohn Company Metallated halogenated acetylene corticoid synthesis
US4357279A (en) * 1981-05-18 1982-11-02 The Upjohn Company Preparation of corticoids from 17-keto steroids
US4411835A (en) * 1981-05-18 1983-10-25 The Upjohn Company Preparation of corticoids from 17-keto steroids
US4404142A (en) * 1981-05-18 1983-09-13 The Upjohn Company Preparation of corticoids from 17-keto steroids
US4412955A (en) * 1981-05-18 1983-11-01 The Upjohn Company Preparation of corticoids from 17-keto steroids
US4401599A (en) * 1981-05-18 1983-08-30 The Upjohn Company Preparation of 21-halo steroids
US4383947A (en) * 1981-07-24 1983-05-17 The Upjohn Company Introduction of a fluorine atom
US4524134A (en) * 1982-07-30 1985-06-18 The Upjohn Company Process for preparing 1,2-dehydro steroids
DE3322120A1 (de) * 1982-07-30 1984-02-02 The Upjohn Co., 49001 Kalamazoo, Mich. Verfahren zur umwandlung von 1,2-gesaettigten 3-ketosteroiden in 1,2-dehydrosteroide
EP0104054A3 (en) * 1982-09-20 1985-10-09 The Upjohn Company 16-methylene-steroids and their preparation
US4704358A (en) * 1982-10-25 1987-11-03 The Upjohn Company Δ1 -dehydrogenation with heat or air-dried B. cyclooxidans
US4684610A (en) * 1983-03-15 1987-08-04 The Upjohn Company Process for converting 1,2-saturated steroids to 1,2-dehydro steroids
US4749649A (en) * 1983-05-16 1988-06-07 The Upjohn Company Microbial Δ1-dehydrogenation process using a scavenger of toxic oxygen
US4618456A (en) * 1984-03-20 1986-10-21 The Upjohn Company Ethynylation of 16-methyl-17-keto steroids
US4614621A (en) * 1984-04-20 1986-09-30 The Upjohn Company Ethynylation of 16-methylene-17-keto steroids
US4548748A (en) * 1984-02-03 1985-10-22 The Upjohn Company Cyanohydrin process
US4831131A (en) * 1984-02-03 1989-05-16 The Upjohn Company 11β,17α-Dihydroxy-17β-cyano-androstanes
US4500461A (en) * 1984-02-03 1985-02-19 The Upjohn Company Cyanohydrin process
US4585590A (en) * 1984-02-03 1986-04-29 The Upjohn Company Cyanohydrin process
US4530795A (en) * 1984-02-27 1985-07-23 The Upjohn Company Process for preparation of 16 α-methyl corticoids from Δ16 -steroids
US4600538A (en) * 1984-08-02 1986-07-15 The Upjohn Company Corticosteroids from 17-keto steroids via 20-cyano-Δ17 (20)-pregnanes
US4613463A (en) * 1984-11-01 1986-09-23 The Upjohn Company Process and intermediates for the preparation of 17 alphahydroxyprogesterones and corticoids from an enol steroid
US5380840A (en) * 1985-09-12 1995-01-10 The Upjohn Company Triazinylpiperazinyl steroids
US5099019A (en) * 1985-09-12 1992-03-24 Upjohn Company Amines useful in producing pharmaceutically active CNS compounds
USRE35053E (en) * 1985-09-12 1995-10-10 The Upjohn Company Amines useful in producing pharmaceutically active CNS compounds
US4910191A (en) * 1988-06-28 1990-03-20 Merrell Dow Pharmaceuticals Inc. 19-substituted progesterone derivatives useful as 19-hydroxylase inhibitors
US5972922A (en) * 1990-06-11 1999-10-26 Alcon Laboratories, Inc. Steroids which inhibit angiogenesis
JPH05507912A (ja) * 1990-06-11 1993-11-11 アルコン・ラボラトリーズ,インコーポレイテッド 血管形成を阻害するステロイド
JP3378245B2 (ja) * 1991-11-22 2003-02-17 アルコン ラボラトリーズ,インコーポレイテッド 血管形成抑制性ステロイド
US20040023935A1 (en) * 2002-08-02 2004-02-05 Dey, L.P. Inhalation compositions, methods of use thereof, and process for preparation of same
US20040109826A1 (en) * 2002-12-06 2004-06-10 Dey, L.P. Stabilized albuterol compositions and method of preparation thereof
HU227112B1 (hu) * 2006-06-14 2010-07-28 Richter Gedeon Nyrt Ipari eljárás 17-alfa-acetoxi-11-béta-[4-(N,N-dimetil-amino)-fenil]-19-norpregna-4,9-dién-3,20-dion elõállítására és új intermedierek az eljáráshoz
EP2805720B1 (en) 2008-05-28 2019-08-07 ReveraGen BioPharma, Inc. Non-hormonal steroid modulators of NF-KB for treatment of disease
EP2556083A4 (en) 2010-04-05 2013-12-04 Validus Biopharma Inc NONHORMONAL STEROID MODULATORS OF NF-KAPPA-B FOR DISEASE TREATMENT
CN102477060B (zh) * 2010-11-22 2014-08-13 华润紫竹药业有限公司 甾体化合物及其制备方法和用途
HUE027821T2 (en) 2011-12-23 2016-11-28 Crystal Pharma Sau A method for alkinylation of 16-substituted-17-ketosteroid derivatives
CN104628806A (zh) * 2012-01-19 2015-05-20 华润紫竹药业有限公司 甾体化合物及其制备方法和用途
CN106046099B (zh) * 2012-01-19 2018-03-16 华润紫竹药业有限公司 甾体化合物及其制备方法和用途
CN102702296B (zh) * 2012-06-19 2014-09-03 山东诚创医药技术开发有限公司 环-3,20-双(1,2-亚乙基缩醛)-17α-羟基-17β-乙酰基-雌甾-5(10),9(11)-二烯-3-酮的制备方法
CN102942612A (zh) * 2012-10-30 2013-02-27 四川大学 一种合成醋酸乌利司他的新方法
WO2014067127A1 (zh) * 2012-11-02 2014-05-08 Huang Yunsheng 一种合成6-甲基-17α-乙酰氧基-19-去甲孕甾-4,6-二烯-3,20-二酮的方法
CN103145788B (zh) * 2013-03-25 2015-08-19 浙江仙琚制药股份有限公司 醋酸优力司特关键中间体的制备方法
WO2017004205A1 (en) 2015-06-29 2017-01-05 Reveragen Biopharma, Inc. NON-HORMONAL STEROID MODULATORS OF NF-κB FOR TREATMENT OF DISEASE
CN105001294A (zh) * 2015-07-29 2015-10-28 宝鸡康乐生物科技有限公司 一种妊娠素的合成方法
CN105153261B (zh) * 2015-10-08 2017-12-05 浙江仙居君业药业有限公司 一种炔孕酮的合成方法
CN106986911B (zh) * 2017-03-23 2019-05-10 湖南玉新药业有限公司 地塞米松关键中间体联烯亚砜物的制备方法
CN106986908B (zh) * 2017-03-23 2019-05-10 湖南玉新药业有限公司 倍他米松的制备方法
US11382922B2 (en) 2019-03-07 2022-07-12 Reveragen Biopharma, Inc. Aqueous oral pharmaceutical suspension compositions
CN112175035A (zh) * 2020-09-08 2021-01-05 山东斯瑞药业有限公司 一种倍他米松重排物的制备方法及倍他米松重排物

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3499016A (en) * 1958-08-04 1970-03-03 Upjohn Co 6alpha-fluoro-16alpha-methyl derivatives of the pregnane series
US3499013A (en) * 1968-11-04 1970-03-03 Searle & Co 3-oxygenated 21beta-hydrocarbonsulfonyl-pregna-17(20),20-dienes,dehydro and 19-nor derivatives thereof and intermediates thereto
FR2150216A1 (en) * 1971-08-20 1973-04-06 Syntex Corp 17-vinylidene steroids - inters for progesterone derivs
US3992422A (en) * 1975-08-14 1976-11-16 Schering Corporation Process for the preparation of 21-halogeno-21-desoxy-17α-acyloxy-20-keto-pregnenes
US4041055A (en) * 1975-11-17 1977-08-09 The Upjohn Company Process for the preparation of 17α-hydroxyprogesterones and corticoids from androstenes

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6354391A (ja) * 1975-11-17 1988-03-08 ジ アツプジヨン カンパニ− ステロイドの製法
JPS6354393A (ja) * 1975-11-17 1988-03-08 ジ アツプジヨン カンパニ− 17α−ヒドロキシステロイド及びその製法
JPH0113719B2 (ja) * 1975-11-17 1989-03-07 Upjohn Co
JPH0113718B2 (ja) * 1975-11-17 1989-03-07 Upjohn Co

Also Published As

Publication number Publication date
GB1531047A (en) 1978-11-01
IE44548L (en) 1977-05-17
IE44548B1 (en) 1981-12-30
PL116356B1 (en) 1981-06-30
JPS6354391A (ja) 1988-03-08
HU173670B (hu) 1979-07-28
JPS6354393A (ja) 1988-03-08
HU178128B (en) 1982-03-28
GB1531048A (en) 1978-11-01
NL7612364A (nl) 1977-05-20
CH636362A5 (de) 1983-05-31
FR2351997B1 (ja) 1980-11-14
JPH0113719B2 (ja) 1989-03-07
GB1531050A (en) 1978-11-01
PL116459B1 (en) 1981-06-30
HU188066B (en) 1986-03-28
HU177914B (en) 1982-01-28
DE2649753C2 (de) 1982-08-19
HU188067B (en) 1986-03-28
IL50787A (en) 1983-06-15
HU178129B (en) 1982-03-28
PL214253A1 (ja) 1980-01-14
JPS6228158B2 (ja) 1987-06-18
GB1531049A (en) 1978-11-01
MX4328E (es) 1982-03-25
IL58539A0 (en) 1980-01-31
FR2351997A1 (fr) 1977-12-16
FR2366310B1 (ja) 1980-11-14
US4041055A (en) 1977-08-09
FR2366310A1 (fr) 1978-04-28
PL215854A1 (ja) 1980-04-21
HU173541B (hu) 1979-06-28
PL119050B1 (en) 1981-11-30
IL50787A0 (en) 1976-12-31
DE2649753A1 (de) 1977-05-26
IL58540A0 (en) 1980-01-31
NL170420C (nl) 1982-11-01
HU174396B (hu) 1979-12-28
PL193723A1 (ja) 1980-01-28
CH630394A5 (de) 1982-06-15
NL170420B (nl) 1982-06-01
JPH0113718B2 (ja) 1989-03-07

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