Reaction equation
[N:1]1[N:5]2[CH:6]=[CH:7][C:8]([C:10](=O)[CH3:11])=[CH:9][C:4]2=[CH:3][CH:2]=1.Cl.S1C2C=C[N:19]=CC=2C=C1CN>>[N:1]1[N:5]2[CH:6]=[CH:7][C:8]([CH:10]([NH2:19])[CH3:11])=[CH:9][C:4]2=[CH:3][CH:2]=1Participants
3
Procedure
Intermediate 3 was prepared from 1-(pyrazolo[1,5-a]pyridin-5-yl)ethanone (3-3) following the procedures similar to the procedures of intermediate D′ from D′-3. MS (m/z): 162 (M+1)+.
Sources & evidence
- ORD record
- ord-974e312f68bd4710b9761ab721738951
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08987269B2
Linked notes
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