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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219499Generated: November 1, 2026

3-Bromo-4-methylpyridine → 6-Methyl-3-(4-methyl-pyridin-3-ylamino)-pyridine-2-carboxylic acid (4-methyl-thiazol-2-yl)-amide

https://huagongshe.com/reaction/2219499

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-4-methylpyridineHCID 817630—
Reactant6-Methyl-3-(pyridin-3-ylamino)-pyridine-2-carboxylic acid (4-methyl-thiazol-2-yl)-amideHCID 11537140—
Product6-Methyl-3-(4-methyl-pyridin-3-ylamino)-pyridine-2-carboxylic acid (4-methyl-thiazol-2-yl)-amideHCID 25096907—

Reaction Steps

The title compound, was prepared from 3-Amino-6-methyl-pyridine-2-carboxylic acid (4-methyl-thiazol-2-yl)-amide (example 14) in accordance with the general method of example 20 using 3-Bromo-4-methylpyridine instead of 3-Bromo-4-methylpyridine to yield the final compound as an off-white solid, MS (ISP): m/e=340.3 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07414060B2
Source datasetuspto-grants-2008_08
ORD IDord-682403a6fb8648a39e4c51f06b3a538d
Source noteuspto-grants-2008_08