HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methoxycarbonyl isothiocyanate → 1-[2-(3-Acetylureido)-5-phenoxysulfonylphenyl]-3-methoxycarbonylthiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methoxycarbonyl isothiocyanate | HCID 552246 | — |
| Reactant | 2-(3-Acetylureido)-5-phenoxysulfonylaniline | HCID 15585384 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-[2-(3-Acetylureido)-5-phenoxysulfonylphenyl]-3-methoxycarbonylthiourea | HCID 15585385 | — |
Reaction Steps
17.5 g of 2-(3-acetylureido)-5-phenoxysulfonylaniline and 15 ml of methoxycarbonyl isothiocyanate in 150 ml of dioxane are heated at 80° C. for 5 minutes, and then stirring is continued without heating. After slowly cooling down to room temperature, the dioxane is distilled out under reduced pressure. The residue is dissolved in dimethylformamide, the solution is treated with active charcoal and evaporated and then methanol is added. After cooling down, the precipitate is filtered off with suction and washed with methanol and diisopropyl ether. Melting point 215° C., decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04504490 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-c789a8dbaaaa4effbd53aff75238dd3a |
| Source note | uspto-grants-1985_03 |