反応式
[C:1]([O:5][C:6](=[O:24])[NH:7][CH:8]([C:12](=[O:23])[NH:13][C:14]1[CH:18]=[C:17]([C:19]([CH3:22])([CH3:21])[CH3:20])[O:16][N:15]=1)[CH2:9][CH2:10]C)([CH3:4])([CH3:3])[CH3:2].NC1C=CON=1>>[C:1]([O:5][C:6](=[O:24])[NH:7][CH:8]([C:12](=[O:23])[NH:13][C:14]1[CH:18]=[C:17]([C:19]([CH3:22])([CH3:21])[CH3:20])[O:16][N:15]=1)[CH2:9][CH3:10])([CH3:3])([CH3:2])[CH3:4]参加物
3
実験手順
Prepared by the analogous method for the preparation of [1-(5-tert-butyl-isoxazol-3-ylcarbamoyl)butyl]-carbamic acid tert-butyl ester, starting with an appropriate amino-isoxazole (1 a-b) together with an appropriate N-t-BOC-amino acid methyl or ethyl ester.
出典と根拠
- ORDレコード
- ord-d7f47e78ef3147b1bb761a63a2b37375
- 出典データセット
- uspto-grants-2007_07
- 特許番号
- US07241786B2
関連ノート
読み込み中…