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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623653Generated: October 29, 2026

2-Chloro-6-methylpyrimidine-4-carboxylic acid → 2-chloro-6-methyl-N-(1-(6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethyl)pyrimidine-4-carb oxamide

https://huagongshe.com/reaction/623653

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6-methylpyrimidine-4-carboxylic acidHCID 10535213—
Reactant1-[6-(2,2,2-Trifluoroethoxy)-pyridin-3-yl]-ethylamine hydrochlorideHCID 67509413—
Product2-chloro-6-methyl-N-(1-(6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethyl)pyrimidine-4-carb oxamideHCID 8742702274%

Reaction Steps

The title compound is prepared in 74% yield (480 mg, clear colorless oil) from (−)-1-(6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethanamine hydrochloride (450 mg, 1.7 mmol, Amine-1, single enantiomer) and 2-chloro-6-methylpyrimidine-4-carboxylic acid (300 mg, 1.7 mmol) by the similar manner in Step-1 of Example 8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302991B2
Source datasetuspto-grants-2016_04
ORD IDord-efcde459cd1a484fa98311c46a3cdd61
Source noteuspto-grants-2016_04