HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 2-[1-Propargyl-3-(5-cyclopropyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 5-Cyclopropyl-1,3,4-thiadiazol-2-yl isocyanate | HCID 53975514 | — |
| Reactant | 2-Propargyl-aminoacetaldehyde | HCID 55285654 | — |
| Product | 2-[1-Propargyl-3-(5-cyclopropyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde | HCID 20392662 | — |
Reaction Steps
A mixture of 5-cyclopropyl-1,3,4-thiadiazol-2-yl isocyanate dimer (7 grams), the dimethyl acetal of 2-propargyl-aminoacetaldehyde (5 grams) and ethyl acetate (50 ml) were 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 2 hours. After this time the mixture is stripped of solvent under reduced pressure to yield the desired product the dimethyl acetal of 2-[1-propargyl-3-(5-cyclopropyl-1,3,4-thiadiazol-2-yl)ureido]-acetaldehyde as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04053480 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-14c3d97f4c8a4b8ab6416fbf396b325e |
| Source note | uspto-grants-1977_10 |