3,5-Dimethylpyrazole → HCID 11848920, compound
Reaction equation
Cl[C:2]1[N:11]=[C:10](Cl)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.[F:13][C:14]([F:23])([F:22])[C:15]1[CH:16]=[C:17]([CH:19]=[CH:20][CH:21]=1)[NH2:18].[CH3:24][C:25]1[CH:29]=[C:28]([CH3:30])[NH:27][N:26]=1>>[CH3:24][C:25]1[CH:29]=[C:28]([CH3:30])[N:27]([C:2]2[N:11]=[C:10]([NH:18][C:17]3[CH:19]=[CH:20][CH:21]=[C:15]([C:14]([F:22])([F:23])[F:13])[CH:16]=3)[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=2)[N:26]=1Participants
4
Procedure
Was prepared according to Method B from 2,4-dichloroquinazoline, 3-trifluoromethylaniline and 3,5-dimethylpyrazole. Mp. 233.1-239.6° C.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-8716957902674f2fbacb84bd26afdf6b
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252806B2
Reaction notes
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