HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-But-3-enylaminopropionaldehyde → 3-[1-But-3-enyl-3-(5-methoxy-1,3,4-thiadiazol-2-yl)ureido]propionaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-But-3-enylaminopropionaldehyde | HCID 21400108 | — |
| Reactant | 5-Methoxy-1,3,4-thiadiazol-2-yl isocyanate | HCID 45123466 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 3-[1-But-3-enyl-3-(5-methoxy-1,3,4-thiadiazol-2-yl)ureido]propionaldehyde | HCID 21400109 | — |
Reaction Steps
A mixture of 5-methoxy-1,3,4-thiadiazol-2-yl isocyanate dimer (0.05 mole), the diethyl acetal 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04053298 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-c9f67813723047abb8e0bea088197706 |
| Source note | uspto-grants-1977_10 |