反応式
[CH3:1][C:2]([O-:5])([CH3:4])[CH3:3].[K+].[Cl:7][C:8]1[C:9]([Cl:18])=[C:10]([Cl:17])[C:11]([Cl:16])=[C:12]([OH:15])[C:13]=1[OH:14].[C:19]([O:23][C:24]([CH:26]1[CH2:30][CH2:29][CH2:28][N:27]1[C:31](=[O:34])[CH2:32]Br)=[O:25])([CH3:22])([CH3:21])[CH3:20]>CN(C)C=O>[C:2]([O:5][C:24]([C@H:26]1[CH2:30][CH2:29][CH2:28][N:27]1[C:31](=[O:34])[CH2:32][O:14][C:13]1[C:8]([Cl:7])=[C:9]([Cl:18])[C:10]([Cl:17])=[C:11]([Cl:16])[C:12]=1[O:15][CH2:32][C:31]([N:27]1[CH2:28][CH2:29][CH2:30][C@@H:26]1[C:24]([O:23][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:25])=[O:34])=[O:23])([CH3:4])([CH3:3])[CH3:1]参加物
5
実験手順
To a solution of 185 mg (1.65 mmol) potassium tert-butylate in 1 ml dimethylformamide at room temperature was added dropwise a solution of 186 mg (0.75 mmol) tetrachlorocatechol in 1 ml dimethylformamide. Stirring was continued for 2-3 min and a solution of 438 mg (1.50 mmol) (R)-(1) -bromoacetyl-pyrrolidine-2-carboxylic acid tert-butyl ester in 2 ml dimethylformamide was added within 1-2 min. The reaction mixture was stirred for additional 4 h at room temperature. The solvent was removed in vacuo and the residue purified by flash-chromatography to yield 229 mg (45%) of the title compound as a white foam. MS m/e (%): 671 (M+H+, 100), 615 (19), 559 (14).
後処理
- stirringThe reaction mixture was stirred for additional 4 h at room temperature
- customThe solvent was removed in vacuo
- customthe residue purified by flash-chromatography
出典と根拠
- ORDレコード
- ord-8440744a0f3447d3b46c4f0f0cb923c7
- 出典データセット
- uspto-grants-2000_08
- 特許番号
- US06103910
関連ノート
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