反応式
[F:1][C:2]1[CH:3]=[C:4]([CH2:8][CH2:9][C:10]([OH:12])=O)[CH:5]=[CH:6][CH:7]=1.[C:13]([O:17][C:18](=[O:30])[NH:19][C:20]1[CH:25]=[C:24]([C:26]([NH:28][NH2:29])=[O:27])[CH:23]=[CH:22][N:21]=1)([CH3:16])([CH3:15])[CH3:14]>>[C:13]([O:17][C:18](=[O:30])[NH:19][C:20]1[CH:25]=[C:24]([C:26]([NH:28][NH:29][C:10](=[O:12])[CH2:9][CH2:8][C:4]2[CH:5]=[CH:6][CH:7]=[C:2]([F:1])[CH:3]=2)=[O:27])[CH:23]=[CH:22][N:21]=1)([CH3:16])([CH3:14])[CH3:15]参加物
3
実験手順
In the same manner as in Reference Example 1 and using 3-(3-fluorophenyl)propionic acid instead of benzothiazole-6-carboxylic acid and tert-butyl[4-(hydrazinocarbonyl)-2-pyridyl]carbamate instead of tert-butyl carbazate, the title compound (yield 60%) was obtained as colorless crystals.
出典と根拠
- ORDレコード
- ord-2c88286c69ad48efb8394d62cacbe8aa
- 出典データセット
- uspto-grants-2013_07
- 特許番号
- US08492378B2
関連ノート
読み込み中…