2-Bromobenzoic acid → 2-(6-Bromo-5-methylpyridin-3-ylamino)benzoic acid

HRID 42046

Reaction equation

HRID 42046 reaction equation
[Br:1][C:2]1[N:7]=[CH:6][C:5]([NH2:8])=[CH:4][C:3]=1[CH3:9].Br[C:11]1[CH:19]=[CH:18][CH:17]=[CH:16][C:12]=1[C:13]([OH:15])=[O:14]>>[Br:1][C:2]1[N:7]=[CH:6][C:5]([NH:8][C:11]2[CH:19]=[CH:18][CH:17]=[CH:16][C:12]=2[C:13]([OH:15])=[O:14])=[CH:4][C:3]=1[CH3:9]

Participants

3

Procedure

Obtained (0.17 g, yield 14%) following the procedure described in Intermediate 13 starting with 6-bromo-5-methylpyridin-3-amine (2.70 mmol, 0.5 g) and 2-bromobenzoic acid (4.03 mmol, 0.81 g).

Workup

  1. customObtained (0.17 g, yield 14%)

Sources & evidence

ORD record
ord-e2d4ee53862b43bbbe2566f95278fedb
Source dataset
uspto-grants-2013_09
Patent number
US08536165B2

Linked notes

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