3,5-Dimethylpyrazole → HCID 25016095, compound
Reaction equation
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([NH:10][C:11]3[N:19]=[C:18](Cl)[N:17]=[C:16]4[C:12]=3[N:13]=[CH:14][N:15]4[CH2:21][CH3:22])=[CH:9][C:4]=2[O:3][CH2:2]1.[CH3:23][C:24]1[CH:28]=[C:27]([CH3:29])[NH:26][N:25]=1>>[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([NH:10][C:11]3[N:19]=[C:18]([N:25]4[C:24]([CH3:23])=[CH:28][C:27]([CH3:29])=[N:26]4)[N:17]=[C:16]4[C:12]=3[N:13]=[CH:14][N:15]4[CH2:21][CH3:22])=[CH:9][C:4]=2[O:3][CH2:2]1Participants
3
Procedure
Was prepared according to Example 6 from benzo[1,3]dioxol-5-yl-(2-chloro-9-ethyl-9H-purin-6-yl)-amine and 3,5-dimethylpyrazole.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-3116b497023b4272a73cd81951cc1ea4
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09340544B2
Reaction notes
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