Lithium Carbonate → Atamestane

HRID 275064

反応式

HRID 275064 の反応式
C(=O)([O-])[O-].[Li+].[Li+].I[C@@H:8]1[C@H:25]([CH3:26])[C@@:24]2([CH3:27])[C:11]([CH2:12][CH2:13][C@@H:14]3[C@@H:23]2[CH2:22][CH2:21][C@@:19]2([CH3:20])[C@H:15]3[CH2:16][CH2:17][C:18]2=[O:28])=[CH:10][C:9]1=[O:29]>CN1CCCC1=O>[CH3:26][C:25]1[C@@:24]2([CH3:27])[C:11]([CH2:12][CH2:13][C@@H:14]3[C@@H:23]2[CH2:22][CH2:21][C@@:19]2([CH3:20])[C@H:15]3[CH2:16][CH2:17][C:18]2=[O:28])=[CH:10][C:9](=[O:29])[CH:8]=1

参加物

4

反応物 2

HCID 11125Lithium CarbonateHCID 677816322alpha-Iodo-1alpha-methylandrost-4-ene-3,17-dione

生成物 1

HCID 57050Atamestane収率 60%

試薬・触媒・溶媒 1

HCID 13387N-methyl-2-pyrrolidone溶媒

実験手順

147.78 mg (2 mmol) of lithium carbonate is heated to 130° C. in 3 ml of N-methyl-pyrrolidone under nitrogen atmosphere. 426 mg (1 mmol) of 2α-iodo-1α-methyl-androst-4-ene-3,17-dione of example 3 is added to this preheated solution. The solution is stirred for another 2 hours at this temperature. After cooling to room temperature, the solution is added in 20 ml of ice water and the product is extracted with ethyl acetate. After evaporation of the solvent, the crude product is purified with ethyl acetate/hexane as mobile solvent by chromatography on silica gel. Concentration by evaporation of the fractions and recrystallization from ethyl acetate yields 178 mg (60% of theory) of 1-methylandrosta-1,4-diene-3,17-dione of melting point 169° C.

後処理

  1. extractionthe product is extracted with ethyl acetate
  2. customAfter evaporation of the solvent
  3. customthe crude product is purified with ethyl acetate/hexane as mobile solvent by chromatography on silica gel
  4. concentrationConcentration
  5. customby evaporation of the fractions and recrystallization from ethyl acetate

出典と根拠

ORDレコード
ord-e048232aa518420dbe795277f166435a
出典データセット
uspto-grants-1995_02
特許番号
US05391778

関連ノート

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