ethyl 3-(5-amino-3-tert-butyl-1H-pyrazol-1-yl)benzoate → 3-[3-tert-Butyl-5-(2,2,2-trichloro-ethoxycarbonylamino)-pyrazol-1-yl]-benzoic acid ethyl ester
反応式
[CH2:1]([O:3][C:4](=[O:21])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([N:11]2[C:15]([NH2:16])=[CH:14][C:13]([C:17]([CH3:20])([CH3:19])[CH3:18])=[N:12]2)[CH:6]=1)[CH3:2].[Cl:22][C:23]([Cl:47])([Cl:46])[CH2:24][O:25][C:26](=[O:45])NC1N(C2C=CC=C(CO)C=2)N=C(C(C)(C)C)C=1>>[CH2:1]([O:3][C:4](=[O:21])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([N:11]2[C:15]([NH:16][C:26]([O:25][CH2:24][C:23]([Cl:47])([Cl:46])[Cl:22])=[O:45])=[CH:14][C:13]([C:17]([CH3:20])([CH3:19])[CH3:18])=[N:12]2)[CH:6]=1)[CH3:2]参加物
3
実験手順
The title compound was prepared from Intermediate 29a using an analogous procedure to that described for Intermediate 29c. LCMS (Method 3): Rt 4.67 min, m/z 462, 464 [MH+].
出典と根拠
- ORDレコード
- ord-4676d0ccadfd49a3beb8890ac0d774ae
- 出典データセット