4-Bromo-1-isopropyl-1H-pyrazole → HCID 71109830, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:22])[C:4]1[CH:9]=[C:8]([S:10][C:11]2[C:19]3[C:14](=[CH:15][C:16]([Cl:20])=[CH:17][CH:18]=3)[NH:13][C:12]=2[CH3:21])[CH:7]=[N:6][CH:5]=1.Br[C:24]1[CH:25]=[N:26][N:27]([CH:29]([CH3:31])[CH3:30])[CH:28]=1>>[CH3:1][O:2][C:3](=[O:22])[C:4]1[CH:9]=[C:8]([S:10][C:11]2[C:19]3[C:14](=[CH:15][C:16]([Cl:20])=[CH:17][CH:18]=3)[N:13]([C:24]3[CH:25]=[N:26][N:27]([CH:29]([CH3:31])[CH3:30])[CH:28]=3)[C:12]=2[CH3:21])[CH:7]=[N:6][CH:5]=1Participants
3
Procedure
Prepared according to the procedure described in Example 3, Step 1, using the following starting materials: 5-(6-chloro-2-methyl-1H-indol-3-ylsulfanyl)-nicotinic acid methyl ester and 4-bromo-1-isopropyl-1H-pyrazole.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-9bd27cdd80224d64b4bf4277156e2cc8
- Source dataset
- uspto-grants-2016_02