[(S)-1-benzyl-4-methyl-4-(3-nitro-phenyl)-6-oxo-1,4,5,6-tetrahydro-pyrimidin-2-yl]-carbamic acid tert-butyl ester → [(S)-4-(3-amino-phenyl)-4-methyl-6-oxo-1,4,5,6-tetrahydro-pyrimidin-2-yl]-carbamic acid tert-butyl ester
反応式
[C:1]([O:5][C:6](=[O:32])[NH:7][C:8]1[N:9](CC2C=CC=CC=2)[C:10](=[O:24])[CH2:11][C@@:12]([CH3:23])([C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([N+:20]([O-])=O)[CH:15]=2)[N:13]=1)([CH3:4])([CH3:3])[CH3:2].C(OC(=O)NC1N(CC2C=CC=CC=2)C(=O)C[C@](C2C=CC=C(N)C=2)(C)N=1)(C)(C)C>C(OCC)(=O)C.CO>[C:1]([O:5][C:6](=[O:32])[NH:7][C:8]1[NH:9][C:10](=[O:24])[CH2:11][C@:12]([C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([NH2:20])[CH:15]=2)([CH3:23])[N:13]=1)([CH3:2])([CH3:3])[CH3:4]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
Starting from [(S)-1-benzyl-4-methyl-4-(3-nitro-phenyl)-6-oxo-1,4,5,6-tetrahydro-pyrimidin-2-yl]-carbamic acid tert-butyl ester (0.98 mmole), the crude material was chromatographed on silica using n-heptane/ethyl acetate (5:2) to give a first fraction containing [(S)-4-(3-amino-phenyl)-1-benzyl-4-methyl-6-oxo-1,4,5,6-tetrahydro-pyrimidin-2-yl]-carbamic acid tert-butyl ester (224 mg) as a colourless foam. MS (ESI): m/z=409.4 [ M+H]+ The second fraction was obtained using ethyl acetate/MeOH (9:1) to give [(S)-4-(3-amino-phenyl)-4-methyl-6-oxo-1,4,5,6-tetrahydro-pyrimidin-2-yl]-carbamic acid tert-butyl ester (49 mg) as a colourless oil. MS (ESI): m/z=319.3 [ M+H]+.
後処理
- customthe crude material was chromatographed on silica
- customto give a first fraction
- customMS (ESI): m/z=409.4 [ M+H]+ The second fraction was obtained
出典と根拠
- ORDレコード
- ord-99174738e65b46118a1c31b93c0af92f
- 出典データセット
- uspto-grants-2013_06
- 特許番号
- US08461160B2
反応ノート
読み込み中…