Acetone → Anecortave Acetate

HRID 65344

반응식

HRID 65344 반응식
[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]

참가 물질

8

반응 조건

온도
15 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-a9ec3ad44eae4e0c8fd779ec69e81f7c
출처 데이터셋
uspto-grants-1986_09
특허 번호
US04613463

연결된 노트

불러오는 중…