HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl [[(methoxycarbonyl)amino](methylthio)methylene]carbamate → HCID 178502035, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl [[(methoxycarbonyl)amino](methylthio)methylene]carbamate | HCID 98708 | — |
| Reactant | 4-(Cyclopropylmethyl-amino)-benzenesulfonic acid 3,4-diamino-phenyl ester | HCID 86596079 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178502035 | HCID 178502035 | 46.7% |
Reaction Steps
To a solution of 4-(cyclopropylmethyl-amino)-benzenesulfonic acid 3,4-diamino-phenyl ester (648 mg) in acetic acid (4.5 ml) and methanol (40 ml) at 80° C. was added 1,3-bis(methoxycarbonyl)-2-methyl-2-thiopseudourea (580 mg). The reaction mixture was refluxed for 4 hours then allowed to cool to ambient temperature and stirred at this temperature for 14 hours. The resultant precipitate was filtered, washed with diethyl ether and dried under vacuum to afford 4-(cyclopropylmethyl-amino)-benzene sulfonic acid 2-methoxycarbonylamino-1H-benzoimidazol-5-yl ester (378 mg) as a beige solid. Mass spectrum: 417 [M+H]+; retention time=13.16 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07041668B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-30c39d20c91f45fb8dc98fc8366c8ac4 |
| Source note | uspto-grants-2006_05 |