O-Methylhydroxylamine → N-Benzyloxy-3-(2-chloro-4-iodo-phenylamino)-isonicotinamide

HRID 78838

Reaction equation

HRID 78838 reaction equation
[Cl: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.[CH3:19][O:20][NH2:21]>>[CH2:19]([O:20][NH:21][C:12](=[O:14])[C:11]1[CH:15]=[CH:16][N:17]=[CH:18][C:10]=1[NH:9][C:3]1[CH:4]=[CH:5][C:6]([I:8])=[CH:7][C:2]=1[Cl:1])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 4113O-MethylhydroxylamineHCID 576496513-[(2-Chloro-4-iodophenyl)amino]isonicotinic acid2×

Product 1

HCID 11677348N-Benzyloxy-3-(2-chloro-4-iodo-phenylamino)-isonicotinamide

Procedure

N-Benzyloxy-3-(2-chloro-4-iodo-phenylamino)-isonicotinamide was synthesized according to the procedure for General Method 1, outlined above, starting with 0.25 mmol of 3-[(2-chloro-4-iodophenyl)amino]isonicotinic acid (intermediate 2) and 0.36 mmol of O-methyl-hydroxylamine. LC/MS [10.01 min; 480 (M+1)]

Workup

  1. customLC/MS [10.01 min; 480 (M+1)]

Sources & evidence

ORD record
ord-b5d33fa1f90b463887abfcf524328a3e
Source dataset
uspto-grants-2014_09
Patent number
US08841459B2

Linked notes

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