3,5-Dimethylpyrazole → HCID 11849090, 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.[NH2:13][C:14]1[CH:15]=[CH:16][CH:17]=[C:18]2[C:23]=1[N:22]=[CH:21][CH:20]=[CH:19]2.[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:13][C:14]3[CH:15]=[CH:16][CH:17]=[C:18]4[C:23]=3[N:22]=[CH:21][CH:20]=[CH:19]4)[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, 8-aminoquinoline and 3,5-dimethylpyrazole. Mp. 183.5-184.8° C.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-d33789069f9e478d92c99a17f4c04e2c
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252806B2
Reaction notes
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