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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395528Generated: November 3, 2026

Dimethylcarbamoyl Chloride → N,N-Dimethyl-N'-(2-dimethylaminoethyl)-N'-(4,6-dimethyl-2-pyridyl)urea Dihydrochloride

https://huagongshe.com/reaction/1395528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylcarbamoyl ChlorideHCID 6598—
ReactantTriethylamineHCID 8471—
Reactant2-(2-Dimethylaminoethylamino)-4,6-dimethylpyridineHCID 12857622—
SolventBenzeneHCID 241—
ProductN,N-Dimethyl-N'-(2-dimethylaminoethyl)-N'-(4,6-dimethyl-2-pyridyl)urea DihydrochlorideHCID 12857640144.9%

Reaction Steps

2-(2-Dimethylaminoethylamino)-4,6-dimethylpyridine (7.73 g, 0.04 mole) and triethylamine (4.8 g, 0.048 mole) are dissolved in 200 ml of anhydrous benzene. Dimethyl carbamoyl chloride (4.85 g, 0.045 mole) is added, the mixture stirred at room temperature for 2 hours and then refluxed four hours. After cooling and dilution with 200 ml of diethyl ether, the triethylamine hydrochloride is filtered off and the filtrate concentrated under vacuum. For purification the crude product is taken up in 200 ml diethyl ether and filtered thru Super-Cel. On addition of ethanolic hydrogen chloride to the filtrate, the product crystallizes and is filtered off to obtain 11 g of solid, m.p. 204°. Recrystallization from 150 ml ethanol and 250 ml diethyl ether yields 10.29 g, m.p. 205°-206° C. (d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04203988
Source datasetuspto-grants-1980_05
ORD IDord-427bab30ae7540f1a8bafa8c6b47b734
Source noteuspto-grants-1980_05