3,5-Dimethylpyrazole → HCID 131729916, 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([NH2:16])[CH2:15][CH2:14]1.[CH3:17][C:18]1[CH:22]=[C:21]([CH3:23])[NH:20][N:19]=1>>[ClH:1].[CH:13]1([NH:16][C:10]2[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=[C:2]([N:19]3[C:18]([CH3:17])=[CH:22][C:21]([CH3:23])=[N:20]3)[N:11]=2)[CH2:15][CH2:14]1Participants
4
Procedure
Was prepared according to Method A from 2,4-dichloroquinazoline, cyclopropylamine and 3,5-dimethylpyrazole. Mp. 254° C.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-af5267f4aef842c89998ad957b98d402
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252806B2
Reaction notes
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