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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380744Generated: November 1, 2026

Triethylamine → 2-Chloro-N-methylnicotinamide

https://huagongshe.com/reaction/380744

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 suspensions 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 numberUS06303790B1
Source datasetuspto-grants-2001_10
ORD IDord-ddf31783291f4d458aab496f0dcaec62
Source noteuspto-grants-2001_10