3,5-Dimethylpyrazole → HCID 131729918, 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.[CH:13]1([NH2:19])[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1.[CH3:20][C:21]1[CH:25]=[C:24]([CH3:26])[NH:23][N:22]=1>>[ClH:1].[CH:13]1([NH:19][C:10]2[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=[C:2]([N:22]3[C:21]([CH3:20])=[CH:25][C:24]([CH3:26])=[N:23]3)[N:11]=2)[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1Participants
4
Procedure
Was prepared according to Method A from 2,4-dichloroquinazoline, cyclohexylamine and 3,5-dimethylpyrazole Mp. 137.6-142.7° C.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-5ecf93d934d044dfab2a151a1d1d7c63
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252806B2
Reaction notes
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