1H-indazole-3-carbohydrazide → HCID 57649647, compound

HRID 78795Notes

Reaction equation

HRID 78795 reaction equation
[F:1][C:2]1[CH:7]=[C:6]([I:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10]1[CH:18]=[N:17][CH:16]=[CH:15][C:11]=1[C:12]([OH:14])=O.[NH:19]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[C:21]([C:28]([NH:30][NH2:31])=[O:29])=[N:20]1>>[F:1][C:2]1[CH:7]=[C:6]([I:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10]1[CH:18]=[N:17][CH:16]=[CH:15][C:11]=1[C:12]([NH:31][NH:30][C:28]([C:21]1[C:22]2[C:27](=[CH:26][CH:25]=[CH:24][CH:23]=2)[NH:19][N:20]=1)=[O:29])=[O:14]

Participants

3

Reactant 2

HCID 27278531H-indazole-3-carbohydrazideHCID 590267913-((2-Fluoro-4-iodophenyl)amino)isonicotinic acid2×

Product 1

HCID 57649647HCID 57649647, compound

Procedure

N′-{3-[(2-fluoro-4-iodophenyl)amino]isonicotinoyl}-1H-indazole-3-carbohydrazide was synthesized according to the procedure for General Method 1, outlined above, starting with 0.32 mmol of 3-[(2-fluoro-4-iodophenyl)amino]isonicotinic acid (intermediate 1) and 0.47 mmol of 1H-indazole-3-carboxylic acid hydrazide. LC/MS [9.14 min; 517 (M+1)]

Workup

  1. customLC/MS [9.14 min; 517 (M+1)]

Sources & evidence

ORD record
ord-2bf678250c784bf7aa706f57a8b6b278
Source dataset
uspto-grants-2014_09
Patent number
US08841459B2

Reaction notes

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