3,5-Dimethylpyrazole → HCID 131729924, 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([NH2:23])[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH2:16][CH2:15][CH2:14]1.[CH3:24][C:25]1[CH:29]=[C:28]([CH3:30])[NH:27][N:26]=1>>[ClH:1].[CH3:24][C:25]1[CH:29]=[C:28]([CH3:30])[N:27]([C:2]2[N:11]=[C:10]([NH:23][CH:13]3[C:22]4[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=4)[CH2:16][CH2:15][CH2:14]3)[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=2)[N:26]=1Participants
4
Procedure
Was prepared according to Method A from 2,4-dichloroquinazoline, 1,2,3,4-tetrahydro-1-naphthylamine and 3,5-dimethylpyrazole. Mp. 221° C.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-d8872ab8fcb3415f849be031604f4df1
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252806B2
Reaction notes
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