3,5-Dimethylpyrazole → HCID 131729932, 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.[NH2:13][CH:14]1[CH2:22][C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH2:15]1.[CH3:23][C:24]1[CH:28]=[C:27]([CH3:29])[NH:26][N:25]=1>>[ClH:1].[CH3:23][C:24]1[CH:28]=[C:27]([CH3:29])[N:26]([C:2]2[N:11]=[C:10]([NH:13][CH:14]3[CH2:22][C:21]4[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=4)[CH2:15]3)[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=2)[N:25]=1Participants
4
Procedure
Was prepared according to Method A from 2,4-dichloroquinazoline, 2-aminoindan and 3,5-dimethylpyrazole. Mp. 212-215° C.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-a958de4ccc444302a60fde758d7b64a8
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08252806B2
Reaction notes
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