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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596733Generated: October 30, 2026

Benzene → 2-[1-Methyl-3-(5-cyclohexyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde

https://huagongshe.com/reaction/596733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantAlaninalHCID 188982—
Reactant2-Cyclohexyl-5-isocyanato-1,3,4-thiadiazoleHCID 53924444—
Product2-[1-Methyl-3-(5-cyclohexyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehydeHCID 20392708—

Reaction Steps

A mixture of 5-cyclohexyl-1,3,4-thiadiazol-2-yl isocyanate dimer (12 grams), the dimethyl acetal of 2-methyl-aminoacetaldehyde (6.9 grams) and benzene (60 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer and reflux condenser. The reaction mixture is heated at reflux for a period of about 15 minutes. After this time the mixture is stripped of benzene under reduced pressure to yield a solid product as the residue. The residue is then recrystallized from methanol to yield the desired product the dimethyl acetal of 2-[1-methyl-3-(5-cyclohexyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde having a melt point of 133° to 134° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04012223
Source datasetuspto-grants-1977_03
ORD IDord-8c33973b3c0e4f719861ec47280035a7
Source noteuspto-grants-1977_03