ES355911A1 - Metodo de obtencion de nuevos 9 beta, 10 alfa esteroides. - Google Patents
Metodo de obtencion de nuevos 9 beta, 10 alfa esteroides.Info
- Publication number
- ES355911A1 ES355911A1 ES355911A ES355911A ES355911A1 ES 355911 A1 ES355911 A1 ES 355911A1 ES 355911 A ES355911 A ES 355911A ES 355911 A ES355911 A ES 355911A ES 355911 A1 ES355911 A1 ES 355911A1
- Authority
- ES
- Spain
- Prior art keywords
- alpha
- compounds
- oxo
- pregn
- ene
- Prior art date
- 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.)
- Expired
Links
- 150000001875 compounds Chemical class 0.000 abstract 12
- -1 1,2-methylene Chemical group 0.000 abstract 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 7
- RJKFOVLPORLFTN-LEKSSAKUSA-N Progesterone Natural products C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H](C(=O)C)[C@@]1(C)CC2 RJKFOVLPORLFTN-LEKSSAKUSA-N 0.000 abstract 3
- 239000006227 byproduct Substances 0.000 abstract 3
- 238000005886 esterification reaction Methods 0.000 abstract 3
- 125000004043 oxo group Chemical group O=* 0.000 abstract 3
- 239000000047 product Substances 0.000 abstract 3
- RJKFOVLPORLFTN-UHFFFAOYSA-N progesterone acetate Natural products C1CC2=CC(=O)CCC2(C)C2C1C1CCC(C(=O)C)C1(C)CC2 RJKFOVLPORLFTN-UHFFFAOYSA-N 0.000 abstract 3
- 239000000126 substance Substances 0.000 abstract 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 230000032050 esterification Effects 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 230000007062 hydrolysis Effects 0.000 abstract 2
- 238000006460 hydrolysis reaction Methods 0.000 abstract 2
- 230000000813 microbial effect Effects 0.000 abstract 2
- 230000003647 oxidation Effects 0.000 abstract 2
- 238000007254 oxidation reaction Methods 0.000 abstract 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 abstract 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 abstract 1
- 239000007868 Raney catalyst Substances 0.000 abstract 1
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 abstract 1
- 229910000564 Raney nickel Inorganic materials 0.000 abstract 1
- 239000003513 alkali Substances 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 239000000969 carrier Substances 0.000 abstract 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 abstract 1
- 238000005695 dehalogenation reaction Methods 0.000 abstract 1
- 230000018044 dehydration Effects 0.000 abstract 1
- 238000006297 dehydration reaction Methods 0.000 abstract 1
- 238000006356 dehydrogenation reaction Methods 0.000 abstract 1
- 238000006704 dehydrohalogenation reaction Methods 0.000 abstract 1
- 150000002084 enol ethers Chemical class 0.000 abstract 1
- 238000006735 epoxidation reaction Methods 0.000 abstract 1
- 238000006266 etherification reaction Methods 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 238000005658 halogenation reaction Methods 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 238000005647 hydrohalogenation reaction Methods 0.000 abstract 1
- 238000005805 hydroxylation reaction Methods 0.000 abstract 1
- LGRLWUINFJPLSH-UHFFFAOYSA-N methanide Chemical compound [CH3-] LGRLWUINFJPLSH-UHFFFAOYSA-N 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- 238000007911 parenteral administration Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- AYGFEWYXKDFVIQ-NWSAAYAGSA-N pregn-4-en-3-one Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H](CC)[C@@]1(C)CC2 AYGFEWYXKDFVIQ-NWSAAYAGSA-N 0.000 abstract 1
- 239000000583 progesterone congener Substances 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J7/00—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J5/00—Normal 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J75/00—Processes for the preparation of steroids in general
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Steroid Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3178567 | 1967-07-11 | ||
GB26719/68A GB1247661A (en) | 1967-07-11 | 1967-07-11 | NEW 9beta,10alpha-STEROIDS AND METHODS OF PRODUCING THE SAME |
Publications (1)
Publication Number | Publication Date |
---|---|
ES355911A1 true ES355911A1 (es) | 1970-01-01 |
Family
ID=26258386
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES355911A Expired ES355911A1 (es) | 1967-07-11 | 1968-07-09 | Metodo de obtencion de nuevos 9 beta, 10 alfa esteroides. |
Country Status (9)
Country | Link |
---|---|
US (1) | US3555053A (en, 2012) |
BE (1) | BE717951A (en, 2012) |
DE (1) | DE1768897A1 (en, 2012) |
ES (1) | ES355911A1 (en, 2012) |
FR (1) | FR8088M (en, 2012) |
GB (1) | GB1247661A (en, 2012) |
IL (1) | IL30329A0 (en, 2012) |
NL (1) | NL6809797A (en, 2012) |
SE (1) | SE345128B (en, 2012) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL7003064A (en, 2012) * | 1970-03-04 | 1971-09-07 | ||
NL7003063A (en, 2012) * | 1970-03-04 | 1971-09-07 | ||
DE2623161C3 (de) * | 1976-05-22 | 1982-02-04 | Gildemeister Ag, 4800 Bielefeld | Einrichtung zur Erzeugung von insbesondere Innengewinden auf Mehrspindel-Drehautomaten |
US4293548A (en) * | 1980-09-02 | 1981-10-06 | Merrell Dow Pharmaceuticals Inc. | 18-Substituted pregn-4-ene-3,20-diones |
DE3402743C2 (de) * | 1984-01-27 | 1986-09-25 | Index-Werke Kg Hahn & Tessky, 7300 Esslingen | Verfahren und Vorrichtung zur Gewindeherstellung |
DE19735340A1 (de) * | 1997-08-14 | 1999-02-18 | Abb Patent Gmbh | Verfahren zum Gewindefräsen |
RU2008116571A (ru) * | 2005-09-30 | 2009-11-10 | Зольвай Фармасьютиклз Гмбх (De) | Новые с18 модифицированные ретростероиды в качестве модулятора рецептора прогестерона |
US20070082876A1 (en) * | 2005-09-30 | 2007-04-12 | Solvay Pharmaceuticals Gmbh | Novel C18 modified retrosteroids as progesterone receptor modulator compounds |
US20070212751A1 (en) * | 2006-01-18 | 2007-09-13 | Solvay Pharmaceuticals Gmbh | Microbial method for the 11beta hydroxylation of 9beta, 10alpha-steriods |
WO2018109622A1 (en) * | 2016-12-15 | 2018-06-21 | Glenmark Pharmaceuticals Limited | Process for preparation of dydrogesterone |
-
1967
- 1967-07-11 GB GB26719/68A patent/GB1247661A/en not_active Expired
-
1968
- 1968-07-08 IL IL30329A patent/IL30329A0/xx unknown
- 1968-07-08 SE SE9406/68A patent/SE345128B/xx unknown
- 1968-07-09 US US743311A patent/US3555053A/en not_active Expired - Lifetime
- 1968-07-09 ES ES355911A patent/ES355911A1/es not_active Expired
- 1968-07-11 BE BE717951D patent/BE717951A/xx unknown
- 1968-07-11 NL NL6809797A patent/NL6809797A/xx unknown
- 1968-07-11 DE DE19681768897 patent/DE1768897A1/de active Pending
- 1968-10-09 FR FR169261A patent/FR8088M/fr not_active Expired
Also Published As
Publication number | Publication date |
---|---|
NL6809797A (en, 2012) | 1969-01-14 |
SE345128B (en, 2012) | 1972-05-15 |
FR8088M (en, 2012) | 1970-07-20 |
GB1247661A (en) | 1971-09-29 |
BE717951A (en, 2012) | 1969-01-13 |
DE1768897A1 (de) | 1971-12-30 |
US3555053A (en) | 1971-01-12 |
IL30329A0 (en) | 1968-09-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3357973A (en) | 7alpha-mono-and dihalomethyl steroids | |
ES355911A1 (es) | Metodo de obtencion de nuevos 9 beta, 10 alfa esteroides. | |
GB1087317A (en) | New, highly active estrogenic 17-oxo-steroids and process for their manufacture | |
US3318922A (en) | 13-substituted alkyl-17-hydroxygona-4-en-3-ones and their 17alpha substitution products | |
ES248593A1 (es) | Un método de producir nuevos esteriodes | |
GB1146992A (en) | Improvements in or relating to novel steroids and the manufacture thereof | |
GB1206873A (en) | 7alpha-METHYL-ANDROSTENE COMPOUNDS | |
Marshall et al. | The total synthesis of (±)-β-vetivone | |
GB1277267A (en) | 07-acetylgonanes and derivatives therefor | |
US3357975A (en) | 7alpha-mono-and dihalomethylestra-4, 9 (10)-dienes and 4, 9 (10), 11-trienes and their preparation | |
GB1083731A (en) | Sulfurenic acid and derivatives thereof | |
US3642841A (en) | 17alpha-substituted 13 - alkyl - 17beta -hydroxygona-4 9-dien-3-ones and 17beta-alkanoates | |
GB1068500A (en) | Improvements in or relating to b-norestrogens | |
GB1425415A (en) | Steroidyl-oestratrienes | |
US3076826A (en) | 17 alpha-(lower-alkyl)-19-nor-5(10)-androstene-3, 17beta-diols | |
US2793208A (en) | Organic compounds | |
US3099659A (en) | Steroidal lactones | |
US3624111A (en) | 18-lower alkyl androstenes | |
US3077484A (en) | 2-formyl androstanes and process therefor | |
US3123600A (en) | Reaction sequence b | |
GB1272102A (en) | Steroid ethers | |
GB1089916A (en) | Novel 17-alkyl-19-nor-steroids | |
US3833644A (en) | B,d-seco-delta4 and delta5(10)-steroidal compounds | |
US3549672A (en) | 3-alkoxy-17-hydroxygona-2,5(10)-dienes | |
US3239509A (en) | 3-desoxy-deta4-androstene 17-tetrahydropyranyl ethers |