3,5-Dimethylpyrazole → HCID 11848970, compound
Reaction equation
Cl[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.[CH3:13][O:14][C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([NH2:21])[CH:16]=1.[CH3:22][C:23]1[CH:27]=[C:26]([CH3:28])[NH:25][N:24]=1>>[CH3:22][C:23]1[CH:27]=[C:26]([CH3:28])[N:25]([C:2]2[N:11]=[C:10]([NH:21][C:17]3[CH:18]=[CH:19][CH:20]=[C:15]([O:14][CH3:13])[CH:16]=3)[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=2)[N:24]=1Participants
4
Procedure
Was prepared according to Method B from 2,4-dichloroquinazoline, m-anisidine and 3,5-dimethylpyrazole. Mp. 193.1-194.7° C.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-9fb8b07a0a3448668541aa61531e1bdf
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252806B2
Reaction notes
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