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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27997Generated: October 26, 2026

Urea → 1-Benzoyl-3-methyl-5-(3-trichloromethyl-1,2,4-thiadiazol-5-yl)biuret

https://huagongshe.com/reaction/27997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUreaHCID 1176—
ReactantBenzoyl isocyanateHCID 78210—
Reactant1-Methyl-3-(3-trichloromethyl-1,2,4-thiadiazol-5-yl)ureaHCID 23341246—
SolventBenzeneHCID 241—
Product1-Benzoyl-3-methyl-5-(3-trichloromethyl-1,2,4-thiadiazol-5-yl)biuretHCID 2334124335.5%

Reaction Conditions

Temperature145 °C

Reaction Steps

A glass pressure vessel was charged with 5.5 grams (0.02 mole) 1-methyl-3-(3-trichloromethyl-1,2,4-thiadiazol-5-yl)urea, 3.2 grams (0.02 mole) benzoyl isocyanate and 50 milliliters benzene. A magnetic stirring bar was added and the vessel sealed. The stirred reaction mixture was heated at 145° C. for 1.5 hours and then allowed to cool to room temperature where 4.5 grams of starting urea precipitates. The urea was removed by filtration and the filtrate concentrated in vacuo to leave 3.0 grams of residue. Extraction of the residue with hot cyclohexane, followed by cooling the extract yielded 0.2 grams (11% selectivity) of pure product; m.p. 70° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04224449
Source datasetuspto-grants-1980_09
ORD IDord-8612e1f7ac334909a950534ef2d2bb70
Source noteuspto-grants-1980_09