Isopropylamine → 1-(diphenylmethyl)-N-(1-methylethyl)-3-[(phenylmethyl)amino]azetidine-3-carboxamide
反応式
[C:1]1([CH:7]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[N:8]2[CH2:11]C(NCC3C=CC=CC=3)(C(O)=O)[CH2:9]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C([N:32](CC)[CH:33]([CH3:35])[CH3:34])(C)C.C[CH:39]([NH2:41])[CH3:40].C([O:45][CH2:46][CH3:47])(=O)C>CN(C=O)C>[C:23]1([CH:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[N:8]2[CH2:9][C:47]([NH:41][CH2:39][C:40]3[CH:5]=[CH:6][CH:1]=[CH:2][CH:3]=3)([C:46]([NH:32][CH:33]([CH3:34])[CH3:35])=[O:45])[CH2:11]2)[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
To a mixture of 1-(diphenylmethyl)-3-[(phenylmethyl)amino]azetidine-3-carboxylic acid (0.50 g, 1.34 mmol), N,N-diisopropylethylamine (0.47 mL, 2.68 mmol) in DMF (3 mL) was added 1-benzotriazolyloxytripyrrolidinylphosphonium hexafluorophosphate (1.34 g, 2.68 mol) and the resulting mixture was stirred at room temperature for 10 minutes. To this mixture was added 2-propylamine (0.22 mL, 2.68 mmol) and stirring was continued for 18 h. The reaction mixture was diluted with ethyl acetate (100 mL) and washed with 2% aqueous citric acid, 5% lithium chloride, and brine solutions (50 mL each), dried over sodium sulfate, filtered and concentrated to give an oily residue which was purified by flash chromatography (silica gel, eluting with 15-25% ethyl acetate-hexane) to give 1-(diphenylmethyl)-N-(1-methylethyl)-3-[(phenylmethyl)amino]azetidine-3-carboxamide (0.51 g, 92% yield), MS (EI) for C27H31N3O: 414 (MH+).
後処理
- stirringstirring
- waitwas continued for 18 h
- washwashed with 2% aqueous citric acid, 5% lithium chloride, and brine solutions (50 mL each)
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated
- customto give an oily residue which
- customwas purified by flash chromatography (silica gel, eluting with 15-25% ethyl acetate-hexane)
出典と根拠
- ORDレコード
- ord-5666c48af14749069f341d6d4c25dbd0
- 出典データセット
- uspto-grants-2011_08
- 特許番号
- US07999006B2
反応ノート
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