HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Butylamino-3-methoxypropionaldehyde → 2-[1-Butyl-3-(5-methylsulfinyl-1,3,4-thiadiazol-2-yl)ureido]-3-methoxypropionaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Butylamino-3-methoxypropionaldehyde | HCID 20357010 | — |
| Reactant | 5-Methylsulfinyl-1,3,4-thiadiazol-2-yl isocyanate | HCID 54084218 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-[1-Butyl-3-(5-methylsulfinyl-1,3,4-thiadiazol-2-yl)ureido]-3-methoxypropionaldehyde | HCID 20357045 | — |
Reaction Steps
5-Methylsulfinyl-1,3,4-thiadiazol-2-yl isocyanate dimer (0.05 mole), the dimethyl acetal of 2-butylamino-3-methoxypropionaldehyde (0.1 mole) and benzene (60 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. The reaction mixture is heated at reflux for a period of about 30 minutes. After this time the mixture is stripped of benzene under reduced pressure to yield a solid product as the residue. This residue is then recrystallized to yield the desired product the dimethyl acetal of 2-[1-butyl-3-(5-methylsulfinyl-1,3,4-thiadiazol-2-yl)ureido]-3-methoxypropionaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04086238 |
| Source dataset | uspto-grants-1978_04 |
| ORD ID | ord-667da1169559438da534ae192b4c19aa |
| Source note | uspto-grants-1978_04 |