3,5-Dimethylpyrazole → HCID 11848975, 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.[CH:13]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:16]=[CH:15][C:14]=1[NH2:23].[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:23][C:14]3[CH:15]=[CH:16][C:17]4[C:22](=[CH:21][CH:20]=[CH:19][CH:18]=4)[CH:13]=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, 2-naphthylamine and 3,5-dimethylpyrazole. Mp. 213.3-215.6° C.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-c3bae477f6c64b5d97b9d66e31a2ce80
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252806B2
Reaction notes
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