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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288395Generated: November 5, 2026

HCID 21501673, compound → HCID 21501685, compound

https://huagongshe.com/reaction/1288395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21501673HCID 21501673—
Reactant5-Allyl-1,3,4-thiadiazol-2-yl isocyanateHCID 53838972—
SolventBenzeneHCID 241—
ProductHCID 21501685HCID 21501685—

Reaction Steps

A mixture of 5-allyl-1,3,4-thiadiazol-2-yl isocyanate dimer (0.05 mole), the dimethyl acetal of 3-chloromethylaminopropionaldehyde (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 the dimethyl acetal of 3-[1-chloromethyl-3-(5-allyl-1,3,4-thiadiazol-2-yl)ureido]propionaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03988143
Source datasetuspto-grants-1976_10
ORD IDord-f46eed6d46ac4ae3b8bd401e7d7bb2c5
Source noteuspto-grants-1976_10