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Fluocortolone

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Fluocortolone Basic information

Product Name:
Fluocortolone
Synonyms:
  • 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,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
  • 6-alpha-fluoro-11-beta,21-dihydroxy-16-alpha-methylpregna-1,4-diene-3,20-dione
  • methylfluorodehydrocorticosterone
  • FLUORCORTOLONE
  • flucortolone
  • Fluocortolon
  • Fluorocortolone
CAS:
152-97-6
MF:
C22H29FO4
MW:
376.46
EINECS:
205-811-5
Product Categories:
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Steroids
Mol File:
152-97-6.mol
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Fluocortolone Chemical Properties

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℃
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Fluocortolone Usage And Synthesis

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

Not classified

FluocortoloneSupplier

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