SU426363A3 - - Google Patents

Info

Publication number
SU426363A3
SU426363A3 SU1695204A SU1695204A SU426363A3 SU 426363 A3 SU426363 A3 SU 426363A3 SU 1695204 A SU1695204 A SU 1695204A SU 1695204 A SU1695204 A SU 1695204A SU 426363 A3 SU426363 A3 SU 426363A3
Authority
SU
USSR - Soviet Union
Prior art keywords
trioxo
difluoro
mixture
pregnadiene
acetoxy
Prior art date
Application number
SU1695204A
Other languages
Russian (ru)
Original Assignee
ностранцы Георг Аннер , Петер Виланд
Ииостранна фирма Циба Гейги
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 ностранцы Георг Аннер , Петер Виланд, Ииостранна фирма Циба Гейги filed Critical ностранцы Георг Аннер , Петер Виланд
Application granted granted Critical
Publication of SU426363A3 publication Critical patent/SU426363A3/ru

Links

Classifications

    • 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J75/00Processes for the preparation of steroids in general

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Steroid Compounds (AREA)

Description

(54) СПОСОБ ПОЛУЧЕНИЯ 6а, 9а-ДИФТОР-16аМЕТИЛ-17а-АЦЕТОКСИ-3 ,11,20-ТРИОКСО-Д -ПРЕГНЕНА(54) METHOD OF OBTAINING 6a, 9a-DIFTOR-16AMETHYL-17A-ACETOXI-3, 11,20-TRIOXO-D-PREGNEN

1212

Изобретение иллюстрируетс  следующим примером.The invention is illustrated by the following example.

Пример. К смеси 3 г ба, 9а-дифтор-16амет ,ил-17а - окси-3,11,20-Т1риок€о-А - прегнадиена и 30 лгуг лед ной уксусной кислоты прибавл ют нри перемешивании и охлаждении, в токе азота в течение 40 мин. 42 мл трифторуксусного ангидрида. После перемешивани  в течение 15 час при комнатной температуре смесь выливают на 400 г льда и медленно прибавл ют 750 мл насышенного раствора би карбоната  атри . Через 30 мин осадок отфильтровывают , промывают водой и раствор ют в хлористом метилене. Раствор отдел ют от воды, сушат и выпаривают в вакууме. Кристаллизацией остатка из смеси хлористый метилен - эфир получают 6а, 9а-дифтор-16аметил-17а-ацетокси - 3,11,20-триоксо-Д - прегпадиен с т. пл. 252-254°С.Example. To a mixture of 3 g of ba, 9a-difluoro-16met, il-17a - oxy-3,11,20-T1riok € o-A - pregnadiene and 30 people of glacial acetic acid are added, with stirring and cooling, in a stream of nitrogen for 40 min 42 ml of trifluoroacetic anhydride. After stirring for 15 hours at room temperature, the mixture is poured onto 400 g of ice and 750 ml of saturated solution of bi-carbonate altri are slowly added. After 30 minutes, the precipitate was filtered, washed with water and dissolved in methylene chloride. The solution is separated from water, dried and evaporated in vacuo. By crystallization of the residue from a mixture of methylene chloride - ether, 6a, 9a-difluoro-16methyl-17a-acetoxy-3,11,20-trioxo-D - pregpadien with m. Pl. 252-254 ° C.

Предмет и з о б р е т е ,н и  Subject and statement of

Способ получени  6а, 9а-дифтор-16а-метил17а-ацетокси-3 ,11,20-триоксо - A-нрегнена или А Прегнадиена формулы IThe method of obtaining 6a, 9a-difluoro-16a-methyl17a-acetoxy-3, 11,20-trioxo-A-nregnen or A Pregnadiene formula I

0-СО-СНСО-СНз0-CO-SNSO-SNZ

отличающийс  тем, что соединение формулы II,characterized in that a compound of formula II,

СО-СНзCO-CH3

где 1,2-св зь может быть насыщена или ненасышена , подвергают ацетилированию с последующим выделением целевого продукта известными приемами.where the 1,2-bond can be saturated or unsaturated, is subjected to acetylation followed by isolation of the target product by known techniques.

SU1695204A 1970-08-28 1971-08-27 SU426363A3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH1291070A CH542831A (en) 1970-08-28 1970-08-28 Process for the preparation of 6a, 9a-difluoro-16a-methyl-17a-acetoxy-3,11,20-trioxo-4-pregnene or -1,4-pregnadiene

Publications (1)

Publication Number Publication Date
SU426363A3 true SU426363A3 (en) 1974-04-30

Family

ID=4387518

Family Applications (1)

Application Number Title Priority Date Filing Date
SU1695204A SU426363A3 (en) 1970-08-28 1971-08-27

Country Status (11)

Country Link
AR (1) AR196989A1 (en)
AT (1) AT312822B (en)
AU (1) AU3275071A (en)
BE (1) BE771900A (en)
BR (1) BR7105636D0 (en)
CH (3) CH542829A (en)
DE (1) DE2141559A1 (en)
FR (1) FR2103585A1 (en)
HU (1) HU162767B (en)
NL (1) NL7111859A (en)
SU (1) SU426363A3 (en)

Also Published As

Publication number Publication date
CH542829A (en) 1973-10-15
BR7105636D0 (en) 1973-05-10
NL7111859A (en) 1972-03-01
CH542831A (en) 1973-10-15
HU162767B (en) 1973-04-28
AR196989A1 (en) 1974-03-08
BE771900A (en) 1972-02-28
AU3275071A (en) 1973-03-01
FR2103585A1 (en) 1972-04-14
AT312822B (en) 1974-01-25
DE2141559A1 (en) 1972-03-02
FR2103585B1 (en) 1974-11-15
CH542833A (en) 1973-10-15

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