GB1283442A - Triamcinolone acetonide esters and preparation thereof - Google Patents
Triamcinolone acetonide esters and preparation thereofInfo
- Publication number
- GB1283442A GB1283442A GB5172870A GB5172870A GB1283442A GB 1283442 A GB1283442 A GB 1283442A GB 5172870 A GB5172870 A GB 5172870A GB 5172870 A GB5172870 A GB 5172870A GB 1283442 A GB1283442 A GB 1283442A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- triamcinolone acetonide
- compounds
- oct
- reaction
- 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
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
- A61K31/573—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone substituted in position 21, e.g. cortisone, dexamethasone, prednisone or aldosterone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/575—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of three or more carbon atoms, e.g. cholane, cholestane, ergosterol, sitosterol
-
- 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
- C07J51/00—Normal steroids with unmodified cyclopenta(a)hydrophenanthrene skeleton not provided for in groups C07J1/00 - C07J43/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J71/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Steroid Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1283442 Triamcinolone acetonide esters SIGMA-TAU INDUSTRIE FARMACEUTICHE RIUNITE SpA 30 Oct 1970 [31 Oct 1969 9 June 1970] 51728/70 Headings C2C and C2U Novel compounds of formula (wherein R is -COCH 3 or -COC 6 H 5 and X is a C 2-10 straight or branched alkylene groups) are prepared from triamcinolone acetonide by reaction with a compound of formula in an inert dry organic solvent at a temp. of 10-50‹ C. in the presence of a hydrogen halideacceptor. Compounds of Formula II are prepared from the corresponding acids by reaction with thionyl chloride. Compounds of Formula I are stated to possess antiphlogistic, thymolytic and glucocorticoid effects and may be made up with carriers into pharmaceutical compositions for topical administration.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT6078469 | 1969-10-31 | ||
IT2572170A IT1045260B (en) | 1970-06-09 | 1970-06-09 | Triamcinolone-acetonide-21-acetyl-n benzyl - carboxylic acid esters |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1283442A true GB1283442A (en) | 1972-07-26 |
Family
ID=26328615
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB5172870A Expired GB1283442A (en) | 1969-10-31 | 1970-10-30 | Triamcinolone acetonide esters and preparation thereof |
Country Status (6)
Country | Link |
---|---|
JP (1) | JPS5335945B1 (en) |
CH (1) | CH534672A (en) |
DK (1) | DK132441C (en) |
FR (1) | FR2070186B1 (en) |
GB (1) | GB1283442A (en) |
IN (1) | IN149611B (en) |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1205537B (en) * | 1961-08-19 | 1965-11-25 | Thomae Gmbh Dr K | Process for making new steroid esters |
-
1970
- 1970-10-26 CH CH1580170A patent/CH534672A/en not_active IP Right Cessation
- 1970-10-30 GB GB5172870A patent/GB1283442A/en not_active Expired
- 1970-10-30 FR FR7039334A patent/FR2070186B1/fr not_active Expired
- 1970-10-30 DK DK553270A patent/DK132441C/en not_active IP Right Cessation
- 1970-10-31 JP JP9635570A patent/JPS5335945B1/ja active Pending
-
1978
- 1978-06-17 IN IN672/CAL/78A patent/IN149611B/en unknown
Also Published As
Publication number | Publication date |
---|---|
DK132441B (en) | 1975-12-08 |
CH534672A (en) | 1973-03-15 |
FR2070186B1 (en) | 1974-08-30 |
IN149611B (en) | 1982-02-13 |
JPS5335945B1 (en) | 1978-09-29 |
DE2047218A1 (en) | 1971-05-13 |
FR2070186A1 (en) | 1971-09-10 |
DK132441C (en) | 1976-05-10 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PE20 | Patent expired after termination of 20 years |