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
Reaction equation
[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]Participants
3
Reactant 2
Product 1
Procedure
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+].
Sources & evidence
- ORD record
- ord-847169bcdaf340ebbe7e5916f9a5f7fc