HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloromethylaminoacetaldehyde → 2-[1-Chloromethyl-3-(5-methylsulfinyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloromethylaminoacetaldehyde | HCID 20392716 | — |
| Reactant | 5-Methylsulfinyl-1,3,4-thiadiazol-2-yl isocyanate | HCID 54084218 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-[1-Chloromethyl-3-(5-methylsulfinyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde | HCID 20392674 | — |
Reaction Steps
A mixture of 5-methylsulfinyl-1,3,4-thiadiazol-2-yl isocyanate dimer (0.05 mole), the dimethyl acetal of 2-chloromethylaminoacetaldehyde (0.1 mole) and benzene (60 ml) is 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 dimethyl acetal of 2-[1-chloromethyl- 3-(5-methylsulfinyl-1,3,4-thiadiazol-2-yl)ureido]-acetaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04053480 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-bf204155b5fd4bee88c372b583b64bf0 |
| Source note | uspto-grants-1977_10 |