HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20324635, compound → HCID 20324617, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20324635 | HCID 20324635 | — |
| Reactant | 5-Methylsulfonyl-1,3,4-thiadiazol-2-yl isocyanate | HCID 54253736 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 20324617 | HCID 20324617 | — |
Reaction Steps
A mixture of 5-methylsulfonyl-1,3,4-thiadiazol-2-yl isocyanate dimer (0.05 mole), the diethyl acetal of 2-(1,1-dimethylprop-2-ynylamino)acetaldehyde (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-(1,1-dimethylprop-2-ynyl)-3-(5-methylsulfonyl-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-be12d50e7c8346b3a1cf3abbe2a05a36 |
| Source note | uspto-grants-1977_06 |