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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839765Generated: October 27, 2026

Dimethylcarbamoyl Chloride → 1,1,3-Trimethyl-3-[5-(beta-chloro-alpha,alpha-dimethylethyl)-1,3,4-thiadiazol-2-yl]urea

https://huagongshe.com/reaction/839765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylcarbamoyl ChlorideHCID 6598—
Reactant5-(1-Chloro-2-methylpropan-2-yl)-N-methyl-1,3,4-thiadiazol-2-amineHCID 12769656—
SolventPyridineHCID 1049—
Product1,1,3-Trimethyl-3-[5-(beta-chloro-alpha,alpha-dimethylethyl)-1,3,4-thiadiazol-2-yl]ureaHCID 2032166189.2%

Reaction Steps

To a solution of 50.0 g of 2-methylamino-5-(β-chloro-α,α-dimethylethyl)-1,3,4-thiadiazole in 300 ml of pyridine was added 46.0 g of dimethyl carbamyl chloride and the reaction heated at reflux temperature for 16 hrs. After cooling, the pyridine was removed on the rotary evaporator and water added to the residue. The reaction was extracted with ether which was shaken with water, saturated sodium chloride and dried over Na2SO4. The solvent was removed at reduced pressure giving 60 g of a viscous oil. Crystallization was effected using a mixture of ether-petroleum ether; wt. 34.5 g (52%), m.p. 80°-82°. Recrystallization from ether-petroleum ether gave the analytical sample, m.p. 82°-83°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04097264
Source datasetuspto-grants-1978_06
ORD IDord-7a63a30b2b5345deabd7801f8db4600b
Source noteuspto-grants-1978_06