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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379408Generated: October 31, 2026

Triethylamine → 2-Chloro-N-methylnicotinamide

https://huagongshe.com/reaction/379408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium CarbonateHCID 10340—
ReactantThionyl ChlorideHCID 24386—
Reactant6-Chloronicotinic acidHCID 79222—
ReactantMethylamine hydrochlorideHCID 6364545—
CatalystDimethylformamideHCID 6228—
SolventTolueneHCID 1140—
SolventSodium chloride; waterHCID 57417360—
Product2-Chloro-N-methylnicotinamideHCID 1228695598.9%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a mixture of 63.0 g (0.40 mol) 6-chloronicotinic acid and 37.7 ml (0.52 mol) thionylchloride was added 340 ml toluene and 0.92 ml (12.0 mmol) DMF. The brown suspension was heated to 95° C. and stirred at 95° C. for 1.5 h. The solvent was subsequently removed and the residue treated with 340 ml CH2Cl2. This solution was cooled to 2° C. and treated with 81.0 g (1.2 mol) methylaminhydrochloride. To the so formed brown suspension was added at −2° C. to −6° C. dropwise over 75 min. 167.5 ml (1.2 mol) NEt3 (the reaction was finished after further 30 min.). The reaction mixture was poured onto 400 ml brine and 100 ml sat. aqueous sodium carbonate and extracted. The aqueous phase was extracted with total 2.4 l CH2Cl2. The organic phases were washed with 400 ml sat. aqueous sodium carbonate and 400 ml brine, combined, dried over MgSO4. The solvent was removed under reduced pressure to give 67.5 g (98.9%) product as brown crystals, m.p. 147.5-148.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06297375B1
Source datasetuspto-grants-2001_10
ORD IDord-b11b6a41b2564af98a53ee6379206571
Source noteuspto-grants-2001_10