Acetone → 21-Desacetoxy-21-Chloro Anecortave

HRID 66551Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 66551
[Cl:1][CH:2]=[C:3]([O:25]C)[C@:4]1([OH:24])[C@:21]2([CH3:22])[C@H:7]([C@H:8]3[C:18](=[CH:19][CH2:20]2)[C@:16]2([CH3:17])[C:11](=[CH:12][C:13](=[O:23])[CH2:14][CH2:15]2)[CH2:10][CH2:9]3)[CH2:6][CH2:5]1.C1COCC1.CC(C)=O.Cl>CCCCCC.CO>[Cl:1][CH2:2][C:3](=[O:25])[C@:4]1([OH:24])[C@:21]2([CH3:22])[C@H:7]([C@H:8]3[C:18](=[CH:19][CH2:20]2)[C@:16]2([CH3:17])[C:11](=[CH:12][C:13](=[O:23])[CH2:14][CH2:15]2)[CH2:10][CH2:9]3)[CH2:6][CH2:5]1

Komponenten

7

Versuchsvorschrift

21-Chloro-17α-hydroxy-20-methoxypregna-4,9(11),20-trien-3-one (VII, Example 4, 1.0 g), THF (4 ml), acetone (4.9 ml), and methanol (1.4 ml) are mixed. Aqueous hydrochloric acid (6 N, 0.44 ml) is added and the resulting slurry heated at 40° for 1.5 hours. The mixture is cooled to 20°-25° and diluted with hexane (3 ml). The solids are isolated by filtration and washed with hexane/ethyl acetate (85/15, 13 ml) to give the title compound.

Aufarbeitung

  1. temperaturethe resulting slurry heated at 40° for 1.5 hours
  2. temperatureThe mixture is cooled to 20°-25°
  3. customThe solids are isolated by filtration
  4. washwashed with hexane/ethyl acetate (85/15, 13 ml)

Quellen und Nachweise

ORD-Eintrag
ord-846a8806a8f34412a7df715c710e35fc
Quelldatensatz
uspto-grants-1982_08
Patentnummer
US04342702

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