4-Isopropylaniline → 4-bromo-N-(4-isopropylphenyl)picolinamide

Reaction equation

[Br:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([C:8]([OH:10])=O)[CH:3]=1.[CH:11]([C:14]1[CH:20]=[CH:19][C:17]([NH2:18])=[CH:16][CH:15]=1)([CH3:13])[CH3:12]>>[Br:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([C:8]([NH:18][C:17]2[CH:19]=[CH:20][C:14]([CH:11]([CH3:13])[CH3:12])=[CH:15][CH:16]=2)=[O:10])[CH:3]=1

Participants

Reactant 2

HCID 74644-Isopropylaniline

HCID 7351504-Bromopyridine-2-carboxylic acid

Product 1

HCID 866958534-bromo-N-(4-isopropylphenyl)picolinamide

Procedure

In a manner similar to that describe in Preparation 34, 4-bromo-pyridine-2-carboxylic acid and 4-isopropylaniline were converted to the title compound.

Sources & evidence

ORD record: ord-344c7c3f2a3d40f5b8bb5f1b023e74a4
Source dataset: uspto-grants-2016_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09388176B2

Reaction notes

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