Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267694Generated: October 29, 2026

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

https://huagongshe.com/reaction/267694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantAlaninalHCID 188982—
Reactant5-Methylsulfonyl-1,3,4-thiadiazol-2-yl isocyanateHCID 54253736—
Product2-[1-Methyl-3-(5-methylsulfonyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehydeHCID 21434236—

Reaction Steps

A mixture of 5-methylsulfonyl-1,3,4-thiadiazol-2-yl isocyanate dimer (0.05 mole), the dimethyl acetal of 2-methyl-aminoacetaldehyde (0.1 mole) 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 to yield the desired product dimethyl acetal of 2-[1-methyl-3-(5-methylsulfonyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03944409
Source datasetuspto-grants-1976_03
ORD IDord-c7f4be55cf5f46c789873328aab6a05e
Source noteuspto-grants-1976_03