3,5-Dimethylpyrazole → HCID 131729929, 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.[C:13]([CH:17]1[CH2:22][CH2:21][CH:20]([NH2:23])[CH2:19][CH2:18]1)([CH3:16])([CH3:15])[CH3:14].[CH3:24][C:25]1[CH:29]=[C:28]([CH3:30])[NH:27][N:26]=1>>[ClH:1].[C:13]([CH:17]1[CH2:18][CH2:19][CH:20]([NH:23][C:10]2[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=[C:2]([N:26]3[C:25]([CH3:24])=[CH:29][C:28]([CH3:30])=[N:27]3)[N:11]=2)[CH2:21][CH2:22]1)([CH3:16])([CH3:14])[CH3:15]Participants
4
Procedure
Was prepared according to Method A from 2,4-dichloroquinazoline, 4-tert-butylcyclohexylamine and 3,5-dimethylpyrazole. Mp. 253-255° C.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-5c7a4015922a4ad3a22b87459a09499c
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252806B2
Reaction notes
Loading…