HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dioxolane-2-methanamine, N-methyl- → N-[5-(N,N-dimethylaminosulfonyl)-1,3,4-thiadiazol-2-yl]-N'-(1,3-dioxolan-2-ylmethyl)-N'-methylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dioxolane-2-methanamine, N-methyl- | HCID 541754 | — |
| Reactant | 5-(N,N-Dimethylaminosulfonyl)-1,3,4-thiadiazol-2-yl isocyanate | HCID 12894454 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-[5-(N,N-dimethylaminosulfonyl)-1,3,4-thiadiazol-2-yl]-N'-(1,3-dioxolan-2-ylmethyl)-N'-methylurea | HCID 12894461 | — |
Reaction Steps
5-(N,N-Dimethylaminosulfonyl)-1,3,4-thiadiazol-2-yl isocyanate dimer (6 grams), N-(1,3-dioxolan-2-ylmethyl)-N-methylamine (6 grams) and ethyl acetate (20 ml) were charged into a glass reaction vessel fitted with a mechanical stirrer. The reaction mixture was heated on a steam bath for a period of about 2 hours. Solvent was then stripped off using a rotary evaporator to yield the desired product N-[5-(N,N-dimethylaminosulfonyl)-1,3,4-thiadiazol-2-yl]-N'-(1,3-dioxolan-2-ylmethyl)-N'-methylurea as the residue. Melting point 100°-110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04255182 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-7a6eb0a19767460d820ab947b30a4bad |
| Source note | uspto-grants-1981_03 |