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ChemicalBook--->CAS DataBase List--->152-97-6

152-97-6

152-97-6 Structure

152-97-6 Structure
IdentificationBack Directory
[Name]

Fluocortolone
[CAS]

152-97-6
[Synonyms]

SH 742
SH-742
flucortolone
Fluocortolon
FLUOCORTOLONE
FLUORCORTOLONE
Fluorocortolone
Fluocortolone USP/EP/BP
Fluocortolone Impurity 13
methylfluorodehydrocorticosterone
Fluocortolone Pivalate EP Impurity A
17alpha-propyl-5alpha-androstan-3-one
Fluocortolone (Fluocortolone Pivalate EPImpurity A)
Fluocortolone Pivalate EP Impurity A (Fluocortolone)
16α-Methyl-6α-fluoro-1,4-pregnadien-11β,21-diol-3,20-dione
(6α,11β,16α)-6-Fluoro-11,21-dihydroxy-16-Methylpregna-1,4-diene-3,20-dione
6-alpha-fluoro-11-beta,21-dihydroxy-16-alpha-methylpregna-1,4-diene-3,20-dione
Pregna-1,4-diene-3,20-dione, 6-fluoro-11,21-dihydroxy-16-methyl-, (6α,11β,16α)-
Fluocortolone Pivalate Impurity 1 (Fluocortolone Pivalate EP Impurity A)(Fluocortolone)
6-fluoro-11-hydroxy-17-(2-hydroxy-1-oxoethyl)-10,13,16-trimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one
(6S,8S,9S,10R,11S,13S,14S,16R,17S)-6-fluoro-17-glycoloyl-11-hydroxy-10,13,16-trimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one
(6s,8s,9r,10s,11s,13s,14s,16r,17s)-6-fluoro-11-hydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one
(6S,8S,9S,10R,11S,13S,14S,16R,17S)-6-fluoro-11-hydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one
(6S,8S,9S,10R,11S,13S,14S,16R,17S)-6-fluoro-11-hydroxy-17-(2-hydroxyethanoyl)-10,13,16-trimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one
[EINECS(EC#)]

205-811-5
[Molecular Formula]

C22H29FO4
[MDL Number]

MFCD00867463
[MOL File]

152-97-6.mol
[Molecular Weight]

376.46
Chemical PropertiesBack Directory
[Melting point ]

113-116°C
[alpha ]

D20 +100° (dioxane)
[Boiling point ]

537.4±50.0 °C(Predicted)
[density ]

1.1001 (estimate)
[vapor pressure ]

0.001Pa at 25℃
[storage temp. ]

Refrigerator
[solubility ]

Chloroform (Slightly), Dioxane (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

12.98±0.10(Predicted)
[color ]

Pale Yellow to Yellow
[Water Solubility ]

204mg/L at 20℃
[LogP]

2.3 at 25℃
Hazard InformationBack Directory
[Chemical Properties]

Pale Yellow Solid
[Originator]

Ultralan,Schering,W. Germany,1965
[Uses]

Fluocortolone is a glucocorticoid used in the treatment of several conditions, including hemorrhoids. Fluocortolone is similar to Fluocortin, but with one less keto group.
[Definition]

ChEBI: Fluocortolone is a 21-hydroxy steroid.
[Manufacturing Process]

(a) 16α-Methyl-6α-Fluoro-δ4-11β,21-Diol-3,20-Dione:16α-methyl-6α-fluoro-δ4- pregnene-21-ol-3,20-dione-21-acetate (MP 132°/134° to 138°C, UVε238= 15,000) is hydroxylated with Curvularia lunata in 11β-position using the fermentation method whereby the 21-acetate group is simultaneously saponified. The hitherto unknown starting material 16α-methyl-6α-fluoro-δ4- pregnene-21-ol-3,20-dione-21-acetate is obtained from 16α-methyl-δ5- pregnene-3β,21-diol-20-one-21-acetate, MP 152° to 154°C, by the addition of bromofluorine (from N-bromoacetamide and hydrogen fluoride) onto the 5-6 double bond, oxidation of the 3β-hydroxyl group with chromic acid, introduction of the δ4-double bond by splitting of the hydrogen bromide and acid isomerization of the 6β-fluoro substituent to the 16α-methyl-6α-fluoro-δ4- pregnene-21-ol-3,20-dione-21-acetate. By chromatographic purification on silica gel the 16α-methyl-6α-fluoro-δ4-pregnene-11β,21-diol-3,20-dione is: MP 166°/167° to 171°C.
(b) 16α-Methyl-6α-Fluoro-δ4-Pregnene-11β,21-Diol-3,20-Dione-21-Acetate:By reaction of the compound of (a) with acetic anhydride in pyridine at room temperature, the acetate is obtained and recrystallized from ethyl acetate, MP 248°/249° to 251°C.
(c) 16α-Methyl-6α-Fluoro-δ1,4-Pregnadiene-11β,21-Diol-3,20-Dione:16α- methyl-6α-fluoro-δ4-pregnene-11β,21-diol-3,20-dione is dehydrogenated with Corynebacterium simplex. The extraction residue is subjected to chromatography on silica gel and after recrystallization there is obtained from methylene chloride-isopropyl ether 16α-methyl-6α-fluoro-δ1,4-pregnadiene- 11β,21-diol-3,20-dione, MP 180°/181° to 182°C.
[Therapeutic Function]

Glucocorticoid
[Flammability and Explosibility]

Notclassified
[storage]

-20°C
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