3,5-Dimethylpyrazole → HCID 131729914, 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.[CH2:13]([NH2:17])[CH2:14][CH2:15][CH3:16].[CH3:18][C:19]1[CH:23]=[C:22]([CH3:24])[NH:21][N:20]=1>>[ClH:1].[CH2:13]([NH:17][C:10]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=[C:2]([N:20]2[C:19]([CH3:18])=[CH:23][C:22]([CH3:24])=[N:21]2)[N:11]=1)[CH2:14][CH2:15][CH3:16]Participants
4
Procedure
Was prepared according to Method A from 2,4-dichloroquinazoline, butylamine and 3,5-dimethylpyrazole. Mp. 98.4° C.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-1a7f5c30e41c4ca1ab01f78074fce0be
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252806B2
Reaction notes
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