Trifluoroacetic acid → 3-((2R)-2-(N-((2R)-2-methylamino-3-(2-naphthyl)propionyl)-N-methylamino)-3-phenylpropionylamino)propyl acetate
反応式
FC(F)(F)C(O)=O.[C:8]([O:11][CH2:12][CH2:13][CH2:14][NH:15][C:16](=[O:50])[C@H:17]([N:25]([C:27](=[O:49])[C@H:28]([N:40](C(OC(C)(C)C)=O)[CH3:41])[CH2:29][C:30]1[CH:39]=[CH:38][C:37]2[C:32](=[CH:33][CH:34]=[CH:35][CH:36]=2)[CH:31]=1)[CH3:26])[CH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)(=[O:10])[CH3:9]>ClCCl>[C:8]([O:11][CH2:12][CH2:13][CH2:14][NH:15][C:16](=[O:50])[C@H:17]([N:25]([C:27](=[O:49])[C@H:28]([NH:40][CH3:41])[CH2:29][C:30]1[CH:39]=[CH:38][C:37]2[C:32](=[CH:33][CH:34]=[CH:35][CH:36]=2)[CH:31]=1)[CH3:26])[CH2:18][C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1)(=[O:10])[CH3:9]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
At 0° C., trifluoroacetic acid (3 mL) was added to a solution of 3-((2R)-2-(N-((2R)-2-(N-(tert-butoxycarbonyl)-N-methylamino)-3-(2-naphthyl)propionyl)-N-methylamino)-3-phenylpropionylamino)propyl acetate (885 mg, 1.50 mmol) in dichloromethane (3 mL). The reaction mixture was stirred for 5 min. The solvents were removed in vacuo at 20° C. The residue was dissolved in dichloromethane (40 mL). The S procedure was repeated twice. The crude product was purified by flash chromatography on silica (45 g) with dichloromethanelmethanol/25% solution of ammonia in water (100:10:1) to give 497 mg of 3-((2R)-2-(N-((2R)-2-methylamino-3-(2-naphthyl)propionyl)-N-methylamino)-3-phenylpropionylamino)propyl acetate.
後処理
- customThe solvents were removed in vacuo at 20° C
- dissolutionThe residue was dissolved in dichloromethane (40 mL)
- customThe crude product was purified by flash chromatography on silica (45 g) with dichloromethanelmethanol/25% solution of ammonia in water (100:10:1)
出典と根拠
- ORDレコード
- ord-3df703c3dbb8431c9cf065eb4d6f2c3f
- 出典データセット
- uspto-grants-2005_09
- 特許番号
- US06939880B2
反応ノート
読み込み中…