HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Methylamino)acetaldehyde → 2-[1-Methyl-3-(5-methylsulfonyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Methylamino)acetaldehyde | HCID 13316132 | — |
| Reactant | 5-Methylsulfonyl-1,3,4-thiadiazol-2-yl isocyanate | HCID 54253736 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-[1-Methyl-3-(5-methylsulfonyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde | HCID 21434236 | — |
Reaction Steps
A mixture of 5-methylsulfonyl-1,3,4-thiadiazol-2-yl isocyanate dimer (0.05 mole), the dimethyl acetal of 2-methylaminoacetaldehyde (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 2-[1-methyl-3-(5-methylsulfonyl-1,3,4-thiadiazol-2-yl)ureido] acetaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04023957 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-48e5e58b2e8c47de8b9c72768edbd8bb |
| Source note | uspto-grants-1977_05 |