2-Aminopyridine → HCID 58614819, compound

HRID 1364751Notes

Reaction equation

HRID 1364751 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[C:11](=[O:26])[NH:12][C:13]1[CH:18]=[CH:17][C:16]([Cl:19])=[C:15]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][N:21]=2)[CH:14]=1)[C:5]([OH:7])=O.[N:27]1[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=1[NH2:33]>>[Cl:1][C:2]1[CH:3]=[C:4]([C:5]([NH:33][C:28]2[CH:29]=[CH:30][CH:31]=[CH:32][N:27]=2)=[O:7])[CH:8]=[CH:9][C:10]=1[C:11]([NH:12][C:13]1[CH:18]=[CH:17][C:16]([Cl:19])=[C:15]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][N:21]=2)[CH:14]=1)=[O:26]

Participants

3

Reactant 2

HCID 104392-AminopyridineHCID 668786053-Chloro-4-(4-chloro-3-(pyridin-2-yl)phenylcarbamoyl)benzoic acid

Product 1

HCID 58614819HCID 58614819, compound

Procedure

50 mg of 3-chloro-4-(4-chloro-3-(pyridin-2-yl)phenylcarbamoyl)benzoic acid was coupled to pyridin-2-amine via Procedure G. The crude product was purified on reverse phase HPLC to yield 2-chloro-N1-(4-chloro-3-(pyridin-2-yl)phenyl)-N4-(pyridin-2-yl)terephthalamide. MS (Q1) 463 (M)+.

Workup

  1. customThe crude product was purified on reverse phase HPLC

Sources & evidence

ORD record
ord-cd969131e71748bda1e0bcfb2b38eef0
Source dataset
uspto-grants-2011_02
Patent number
US07888364B2

Reaction notes

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