Ammonium Acetate → 3-[(2-Fluoro-4-iodophenyl)amino]isonicotinamide

HRID 218889Notes

Reaction equation

HRID 218889 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](O)=[O:13].C([O-])(=O)C.[NH4+:23]>>[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]([NH2:23])=[O:13]

Participants

3

Reactant 2

HCID 517165Ammonium AcetateHCID 590267913-((2-Fluoro-4-iodophenyl)amino)isonicotinic acid2×

Product 1

HCID 116461283-[(2-Fluoro-4-iodophenyl)amino]isonicotinamide

Procedure

3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide was synthesized according to the procedure for General Method 1, outlined above, starting with 8 mmol of 3-[(2-fluoro-4-iodophenyl)amino]isonicotinic acid (intermediate 1) and 16 mmol of. ammonium acetate. LC/MS [7.27 min; 358 (M+1)].

Workup

  1. customLC/MS [7.27 min; 358 (M+1)]

Sources & evidence

ORD record
ord-439ca673853847d6ab181cb779cfc767
Source dataset
uspto-grants-2012_06
Patent number
US08198457B2

Reaction notes

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