HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Propargylaminoacetaldehyde → 2-[1-Propargyl-3-(5-methyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Propargylaminoacetaldehyde | HCID 20392754 | — |
| Reactant | 2-Isocyanato-5-methyl-1,3,4-thiadiazole | HCID 54282028 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-[1-Propargyl-3-(5-methyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde | HCID 20324614 | — |
Reaction Steps
A mixture of 5-methyl-1,3,4-thiadiazol-2-yl isocyanate dimer (0.05 mole), the diethyl acetal of 2-propargylaminoacetaldehyde (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 diethyl acetal of 2-[1-propargyl-3-(5-methyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04028375 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-c9f9e197710f4490a781cad755b89dda |
| Source note | uspto-grants-1977_06 |