Triethylamine → 20,20-Ethylenedioxy-2alpha-methyl-5alpha-pregnane-3,11-dione

HRID 1606487ノート

反応式

HRID 1606487 の反応式
P(OC)(OC)OC.C(N(CC)CC)C.[CH2:15]1[CH2:43][O:42][C:17]([C@@H:19]2[C@:36]3([CH3:37])[C@H:22]([C@H:23]4[C@H:33]([C:34](=[O:38])[CH2:35]3)[C@:31]3([CH3:32])[C@H:26]([CH2:27][C:28](=[O:41])[C:29](=[CH:39]O)[CH2:30]3)[CH2:25][CH2:24]4)[CH2:21][CH2:20]2)([CH3:18])[O:16]1>C(O)(C)C.O.Cl.Cl.Cl[Ir](Cl)(Cl)Cl>[CH2:43]1[CH2:15][O:16][C:17]([C@@H:19]2[C@:36]3([CH3:37])[C@H:22]([C@H:23]4[C@H:33]([C:34](=[O:38])[CH2:35]3)[C@:31]3([CH3:32])[C@H:26]([CH2:27][C:28](=[O:41])[C@H:29]([CH3:39])[CH2:30]3)[CH2:25][CH2:24]4)[CH2:21][CH2:20]2)([CH3:18])[O:42]1

参加物

6

実験手順

A solution of chloroiridic acid (30 mg.) and trimethyl phosphite (4.5 ml.) in aqueous 90% isopropanol (60 ml.) was heated under reflux for 17 hr. The solution was then neutralised with triethylamine and 20,20-ethylenedioxy 2-hydroxymethylene-5α-pregnane-3,11-dione (2 g.) was added. The mixture was heated under reflux for 40 hr. then cooled and partitioned between water and methylene chloride. The organic layer was dried (MgSO4) and evaporated in vacuo. The residue (1.94 g.) was subjected to preparative t.l.c. giving two fractions. The less polar fraction (0.18 g.) was crystallised from methanol to give 20,20-ethylenedioxy-2α-methyl-5α-pregnane-3,11-dione (0.13 g.), m.p. 179°-180°, [α]D + 77.5°.

後処理

  1. temperatureunder reflux for 17 hr
  2. additionwas added
  3. temperatureThe mixture was heated
  4. temperatureunder reflux for 40 hr
  5. temperaturethen cooled
  6. custompartitioned between water and methylene chloride
  7. dry with materialThe organic layer was dried (MgSO4)
  8. customevaporated in vacuo
  9. customgiving two fractions
  10. customThe less polar fraction (0.18 g.) was crystallised from methanol

出典と根拠

ORDレコード
ord-697ca9dfd62f4d70aedfd9132700c478
出典データセット
uspto-grants-1976_04
特許番号
US03953429

反応ノート

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