HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Allylaminopropionaldehyde → 3-[1-Allyl-3-(5-methylsulfonyl-1,3,4-thiadiazol-2-yl)ureido]propionaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Allylaminopropionaldehyde | HCID 21400091 | — |
| Reactant | 5-Methylsulfonyl-1,3,4-thiadiazol-2-yl isocyanate | HCID 54253736 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 3-[1-Allyl-3-(5-methylsulfonyl-1,3,4-thiadiazol-2-yl)ureido]propionaldehyde | HCID 21400077 | — |
Reaction Steps
A mixture of 5-methylsulfonyl-1,3,4-thiadiazol-2-yl isocyanate dimer (0.05 mole), the dimethyl acetal of 3-allylaminopropionaldehyde (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-allyl-3-(5-methylsulfonyl-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-59636f28203b44248cd1e60aca1f4cf9 |
| Source note | uspto-grants-1977_10 |