Reaction equation
[NH:1]([C:3]1[CH:8]=[C:7]([C:9]#[N:10])[CH:6]=[CH:5][N:4]=1)[NH2:2].C[O:12][CH2:13][C:14](=O)[CH2:15][C:16]([O:18][CH3:19])=O>>[OH:12][C:13]1[N:1]([C:3]2[CH:8]=[C:7]([C:9]#[N:10])[CH:6]=[CH:5][N:4]=2)[N:2]=[C:15]([CH2:16][O:18][CH3:19])[CH:14]=1Participants
3
Procedure
The title compound was prepared in 39% yield from 2-hydrazinylpyridine-4-carbonitrile (PREPARATION 2) and methyl 4-methoxy-3-oxobutanoate according to the procedure for the preparation of Example 3, part A. [M+H] Calc'd for C11H10N4O2, 231. Found, 231.
Sources & evidence
- ORD record
- ord-6db4a19df11942199e101559947264ff
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09107916B2
Linked notes
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