3,5-Dimethylpyrazole → HCID 131729912, 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]([NH2:15])[CH3:14].[CH3:16][C:17]1[CH:21]=[C:20]([CH3:22])[NH:19][N:18]=1>>[ClH:1].[CH3:16][C:17]1[CH:21]=[C:20]([CH3:22])[N:19]([C:2]2[N:11]=[C:10]([NH:15][CH2:13][CH3:14])[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=2)[N:18]=1Participants
4
Procedure
Was prepared according to Method A from 2,4-dichloroquinazoline, ethylamine and 3,5-dimethylpyrazole. Mp. 286° C.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-43c57d1429b64df0a7fe0f35b96d2fa7
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252806B2
Reaction notes
Loading…