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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435541Generated: October 29, 2026

3-But-3-enylaminopropionaldehyde → 3-[1-But-3-enyl-3-(5-methoxy-1,3,4-thiadiazol-2-yl)ureido]propionaldehyde

https://huagongshe.com/reaction/435541

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-But-3-enylaminopropionaldehydeHCID 21400108—
Reactant5-Methoxy-1,3,4-thiadiazol-2-yl isocyanateHCID 45123466—
SolventBenzeneHCID 241—
Product3-[1-But-3-enyl-3-(5-methoxy-1,3,4-thiadiazol-2-yl)ureido]propionaldehydeHCID 21400109—

Reaction Steps

A mixture of 5-methoxy-1,3,4-thiadiazol-2-yl isocyanate dimer (0.05 mole), the diethyl acetyl of 3-but-3-enylaminopropionaldehyde (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 the desired product the diethyl acetal of 3-[1-but-3-enyl-3-(5-methoxy-1,3,4-thiadiazol-2-yl)ureido]propionaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04006009
Source datasetuspto-grants-1977_02
ORD IDord-f6d6719c689449f3b10029134086f579
Source noteuspto-grants-1977_02