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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylcarbamoyl Chloride | HCID 6598 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(2-Dimethylaminoethylamino)-4,6-dimethylpyridine | HCID 12857622 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N,N-Dimethyl-N'-(2-dimethylaminoethyl)-N'-(4,6-dimethyl-2-pyridyl)urea Dihydrochloride | HCID 12857640 | 144.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04203988 |
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| Source dataset | uspto-grants-1980_05 |
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| ORD ID | ord-427bab30ae7540f1a8bafa8c6b47b734 |
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| Source note | uspto-grants-1980_05 |
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