(2S,4R)-1-(1-carbamoyl-1H-indol-3-ylcarbamoyl)-4-fluoro-pyrrolidine-2-carboxylic acid benzyl ester → (2S,4R)-1-(1-Carbamoyl-1H-indol-3-ylcarbamoyl)-4-fluoro-pyrrolidine-2-carboxylic acid
反応式
C([O:8][C:9]([C@@H:11]1[CH2:15][C@@H:14]([F:16])[CH2:13][N:12]1[C:17](=[O:31])[NH:18][C:19]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[N:21]([C:28](=[O:30])[NH2:29])[CH:20]=1)=[O:10])C1C=CC=CC=1>C1COCC1.[Pd]>[C:28]([N:21]1[C:22]2[C:27](=[CH:26][CH:25]=[CH:24][CH:23]=2)[C:19]([NH:18][C:17]([N:12]2[CH2:13][C@H:14]([F:16])[CH2:15][C@H:11]2[C:9]([OH:10])=[O:8])=[O:31])=[CH:20]1)(=[O:30])[NH2:29]参加物
4
実験手順
To a solution of (2S,4R)-1-(1-carbamoyl-1H-indol-3-ylcarbamoyl)-4-fluoro-pyrrolidine-2-carboxylic acid benzyl ester (2.5 g, 5.89 mmol) in THF (40 mL) was added Pd/C 10% (500 mg). Air was removed from the flask under high vacuum and replaced with nitrogen, this operation was repeated three times and finally nitrogen was removed and replaced with hydrogen. The mixture was stirred under a hydrogen atmosphere for 16 h. Hydrogen was removed under vacuum and replaced with nitrogen and the catalyst was removed by filtration over a pad of Celite and washed with THF. Solvents were concentrated to give the title product. MS (LC/MS): 335.0 [M+H]+, 691.2 [2M+Na]+, 333.1 [M−H]−; tR (HPLC conditions a): 2.22 min.