Acetone → Anecortave Acetate

HRID 65344

反応式

HRID 65344 の反応式
[OH:1][C@:2]1([C@:28]2([CH3:29])[C@H:14]([C@H:15]3[C:25](=[CH:26][CH2:27]2)[C@:23]2([CH3:24])[C:18](=[CH:19][C:20](=[O:30])[CH2:21][CH2:22]2)[CH2:17][CH2:16]3)[CH2:13][CH2:12]1)[C:3]([O:5]C1C=CC=CC=1)=[CH2:4].P([O-])([O-])([O-])=O.[K+].[K+].[K+].OOS([O-])=O.[K+].[OH-:45].[K+].C[C:48]([CH3:50])=[O:49]>O.C1(C)C=CC=CC=1.C(Cl)Cl>[OH:1][C@:2]1([C@:28]2([CH3:29])[C@H:14]([C@H:15]3[C:25](=[CH:26][CH2:27]2)[C@:23]2([CH3:24])[C:18](=[CH:19][C:20](=[O:30])[CH2:21][CH2:22]2)[CH2:17][CH2:16]3)[CH2:13][CH2:12]1)[C:3](=[O:4])[CH2:5][O:49][C:48](=[O:45])[CH3:50]

参加物

8

反応条件

温度
15 °C

実験手順

17α-hydroxy-20-phenoxypregna-4,9(11),20-trien-3-one (4.05 grams, 10 mmoles) is slurried with 210 ml of an aqueous pH 8 potassium phosphate buffer (0.5M in PO4 ≡), 20 ml of acetone, 40 ml of toluene/methylene chloride (3:2) and n-tetrabutylammonium bromide is (0.645 grams, 2.0 mmole) added. The pH is adjusted to 7.0 to 8.0 and the mixture cooled to 15° C. and an OXONE® solution is (18.4 gms, 30 mmoles dissolved in 65 ml of water) added dropwise by an addition funnel while stirring and maintaining pH at 7.0 to 8.0 by addition of a 30% potassium hydroxide solution. The reaction is worked up by separating the layers and replacing the organic solvent with toluene to a volume of 100 ml so as to remove water. After cooling to 10° C., 3 ml of glacial acetic acid is added. The product is isolated by replacing the toluene with acetone and filtering to obtain 3.12 g of 17α-hydroxy-21-acetoxypregna-4,9(11)-diene-3,20-dione.

後処理

  1. additionadded
  2. additionadded dropwise by an addition funnel
  3. temperaturemaintaining pH at 7.0 to 8.0
  4. customby separating the layers
  5. customto remove water
  6. temperatureAfter cooling to 10° C.
  7. addition3 ml of glacial acetic acid is added
  8. customThe product is isolated
  9. filtrationfiltering

出典と根拠

ORDレコード
ord-a9ec3ad44eae4e0c8fd779ec69e81f7c
出典データセット
uspto-grants-1986_09
特許番号
US04613463

関連ノート

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