ES321329A1 - Un procedimiento de preparacion de derivados del estratrieno7-alfa-metilados. - Google Patents

Un procedimiento de preparacion de derivados del estratrieno7-alfa-metilados.

Info

Publication number: ES321329A1
Authority: ES; Spain
Prior art keywords: formula; see formula; see; des; estrane
Prior art date: 1965-09-03
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

Application number

ES0321329A

Other languages

English (en)

Spanish (es)

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.)

Sanofi Aventis France

Original Assignee

Roussel Uclaf SA

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.)

1965-09-03

Filing date

1965-12-30

Publication date

1966-07-16

1965-09-03 Priority claimed from FR30381A external-priority patent/FR1456779A/fr

1965-12-30 Application filed by Roussel Uclaf SA filed Critical Roussel Uclaf SA

1966-07-16 Publication of ES321329A1 publication Critical patent/ES321329A1/es

Status Expired legal-status Critical Current

Links

238000000034 method Methods 0.000 title abstract 2
238000002360 preparation method Methods 0.000 title abstract 2
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 abstract 3
239000004215 Carbon black (E152) Substances 0.000 abstract 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
238000005903 acid hydrolysis reaction Methods 0.000 abstract 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
150000002148 esters Chemical class 0.000 abstract 2
229930195733 hydrocarbon Natural products 0.000 abstract 2
239000001257 hydrogen Substances 0.000 abstract 2
229910052739 hydrogen Inorganic materials 0.000 abstract 2
-1 methyl magnesium halide Chemical class 0.000 abstract 2
230000003647 oxidation Effects 0.000 abstract 2
238000007254 oxidation reaction Methods 0.000 abstract 2
239000001301 oxygen Substances 0.000 abstract 2
229910052760 oxygen Inorganic materials 0.000 abstract 2
238000007127 saponification reaction Methods 0.000 abstract 2
229920006395 saturated elastomer Polymers 0.000 abstract 2
HLCRYAZDZCJZFG-BDXSIMOUSA-N (8s,9s,13s,14s)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene Chemical compound C1CC2=CC=CC=C2[C@@H]2[C@@H]1[C@@H]1CCC[C@@]1(C)CC2 HLCRYAZDZCJZFG-BDXSIMOUSA-N 0.000 abstract 1
WLIADPFXSACYLS-RQOWECAXSA-N (z)-1,3-dichlorobut-2-ene Chemical compound C\C(Cl)=C\CCl WLIADPFXSACYLS-RQOWECAXSA-N 0.000 abstract 1
150000004057 1,4-benzoquinones Chemical class 0.000 abstract 1
102000004190 Enzymes Human genes 0.000 abstract 1
108090000790 Enzymes Proteins 0.000 abstract 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
230000031709 bromination Effects 0.000 abstract 1
238000005893 bromination reaction Methods 0.000 abstract 1
150000001875 compounds Chemical class 0.000 abstract 1
239000007859 condensation product Substances 0.000 abstract 1
150000001879 copper Chemical class 0.000 abstract 1
230000018044 dehydration Effects 0.000 abstract 1
238000006297 dehydration reaction Methods 0.000 abstract 1
150000002081 enamines Chemical class 0.000 abstract 1
150000002164 estratrienes Chemical class 0.000 abstract 1
230000022244 formylation Effects 0.000 abstract 1
238000006170 formylation reaction Methods 0.000 abstract 1
238000006197 hydroboration reaction Methods 0.000 abstract 1
238000006317 isomerization reaction Methods 0.000 abstract 1
150000002576 ketones Chemical class 0.000 abstract 1
CFHIDWOYWUOIHU-UHFFFAOYSA-N oxomethyl Chemical compound O=[CH] CFHIDWOYWUOIHU-UHFFFAOYSA-N 0.000 abstract 1
AZQWKYJCGOJGHM-UHFFFAOYSA-N para-benzoquinone Natural products O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 abstract 1

Landscapes

Steroid Compounds (AREA)

ES0321329A 1965-09-03 1965-12-30 Un procedimiento de preparacion de derivados del estratrieno7-alfa-metilados. Expired ES321329A1 (es)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR30381A FR1456779A (fr)	1964-12-31	1965-09-03	Dérivés de l'estratriène substitués en position 7 et procédé de préparation

Publications (1)

Publication Number	Publication Date
ES321329A1 true ES321329A1 (es)	1966-07-16

Family

ID=8587747

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES0321329A Expired ES321329A1 (es)	1965-09-03	1965-12-30	Un procedimiento de preparacion de derivados del estratrieno7-alfa-metilados.

Country Status (2)

Country	Link
AT (1)	AT269380B (de)
ES (1)	ES321329A1 (de)

1965
- 1965-12-30 ES ES0321329A patent/ES321329A1/es not_active Expired
1966
- 1966-09-05 AT AT839966A patent/AT269380B/de active

Also Published As

Publication number	Publication date
AT269380B (de)	1969-03-10

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