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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177141Generated: November 1, 2026

5-Bromopyrimidine-2-carboxylic acid → 5-bromo-N,N-dimethylpyrimidine-2-carboxamide

https://huagongshe.com/reaction/1177141

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromopyrimidine-2-carboxylic acidHCID 16462970—
Reactant5-bromo-N,N-dimethylpicolinamideHCID 22831618—
Product5-bromo-N,N-dimethylpyrimidine-2-carboxamideHCID 59559990—

Reaction Steps

The title compound was prepared in a similar manner as described for Intermediate 161a, from 5-bromopyrimidine-2-carboxylic acid (1.03 g, 5.074 mmol) to give a yellow oil (308 mg, 26% yield). 1H NMR (400 MHz, CDCl3) δ 8.50 (s, 2 H) 3.17 (s, 3 H) 3.00 (s, 3 H); LCMS for C7H8BrN3O m/z 230.00 and 232.00 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842713B2
Source datasetuspto-grants-2010_11
ORD IDord-dcc375404c884b378aea8c2afc619e58
Source noteuspto-grants-2010_11