2-Bromobenzoic acid → 2-(6-Bromo-5-methylpyridin-3-ylamino)benzoic acid
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
- customObtained (0.17 g, yield 14%)
Sources & evidence
- ORD record
- ord-e2d4ee53862b43bbbe2566f95278fedb
- Source dataset
- uspto-grants-2013_09
- Patent number
- US08536165B2
Reaction notes
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