Ammonium Acetate → 2-Chloro-3-(2-fluoro-4-iodo-phenylamino)-isonicotinamide
Reaction equation
[Cl:1][C:2]1[C:3]([NH:11][C:12]2[CH:17]=[CH:16][C:15]([I:18])=[CH:14][C:13]=2[F:19])=[C:4]([CH:8]=[CH:9][N:10]=1)[C:5](O)=[O:6].C([O-])(=O)C.[NH4+:24]>>[Cl:1][C:2]1[C:3]([NH:11][C:12]2[CH:17]=[CH:16][C:15]([I:18])=[CH:14][C:13]=2[F:19])=[C:4]([CH:8]=[CH:9][N:10]=1)[C:5]([NH2:24])=[O:6]Participants
3
Procedure
2-Chloro-3-(2-fluoro-4-iodo-phenylamino)-isonicotinamide was synthesized according to the procedure for General Method 1, outlined above, starting with 0.2 mmol of 2-Chloro-3-(2-fluoro-4-iodo-phenylamino)-isonicotinic acid and 0.5 mmol of ammonium acetate. LC/MS [8.61 min; 392 (M+1)].
Workup
- customLC/MS [8.61 min; 392 (M+1)]
Sources & evidence
- ORD record
- ord-29d5ea4b06584737aa13b64e59ea5915
- Source dataset
- uspto-grants-2013_09
- Patent number
- US08524911B2
Reaction notes
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