3,5-Dimethylpyrazole → HCID 131729920, compound
Reaction equation
[Cl:1][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.[NH:13]1[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1.[CH3:19][C:20]1[CH:24]=[C:23]([CH3:25])[NH:22][N:21]=1>>[ClH:1].[CH3:19][C:20]1[CH:24]=[C:23]([CH3:25])[N:22]([C:2]2[N:11]=[C:10]([N:13]3[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]3)[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=2)[N:21]=1Participants
4
Procedure
Was prepared according to Method A from 2,4-dichloroquinazoline, piperidine and 3,5-dimethylpyrazole. Mp. 157° C.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-a44cc2324fb744e48792daec8d312c42
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252806B2
Reaction notes
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