HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Methylamino)acetaldehyde → 2-[1-Methyl-3-(5-cyclohexyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Methylamino)acetaldehyde | HCID 13316132 | — |
| Reactant | 2-Cyclohexyl-5-isocyanato-1,3,4-thiadiazole | HCID 53924444 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-[1-Methyl-3-(5-cyclohexyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde | HCID 20392708 | — |
Reaction Steps
A mixture of 5-cyclohexyl-1,3,4-thiadiazol-2-yl isocyanate dimer (12 grams), the dimethyl acetal of 2-methylaminoacetaldehyde (6.9 grams) 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 from methanol to yield the desired product the dimethyl acetal of 2-[1-methyl-3-(5-cyclohexyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde having a melt point of 133° to 134° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04008068 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-5da8852f9bc149b0b9ddeb6fdcdc563e |
| Source note | uspto-grants-1977_02 |