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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364607Generated: October 28, 2026

2-Methyl-6-(trifluoromethyl)nicotinoyl chloride → N-(4-Chloro-3-iodophenyl)-6-(trifluoromethyl)-2-methylpyridine-3-carboxamide

https://huagongshe.com/reaction/1364607

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-6-(trifluoromethyl)nicotinoyl chlorideHCID 2775675—
Reactant4-Chloro-3-iodoanilineHCID 21874954—
ProductN-(4-Chloro-3-iodophenyl)-6-(trifluoromethyl)-2-methylpyridine-3-carboxamideHCID 66877122—

Reaction Steps

Procedure D was performed with 4-chloro-3-iodoaniline (225 mg, 0.889 mmol) and 6-(trifluoromethyl)-2-methylpyridine-3-carbonyl chloride (237 mg, 0/93 mmol, 1.05 eq) at 0° C. for 30 minutes. The crude residue was purified by silica gel chromatography (2-50% ethyl acetate/hexanes) to yield N-(4-chloro-3-iodophenyl)-6-(trifluoromethyl)-2-methylpyridine-3-carboxamide as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888364B2
Source datasetuspto-grants-2011_02
ORD IDord-b2632a48206a496e9a14be9dd50fdc79
Source noteuspto-grants-2011_02