HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(Diphenoxymethylene)-methanesulfonamide → N-methanesulfonyl-N'-[2-[[5-[N-methyl-N-(2,2,2-trichloroethoxycarbonyl)aminomethyl]-2furyl]methylthio]ethyl]-O-phenylisourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(Diphenoxymethylene)-methanesulfonamide | HCID 13738851 | — |
| Reactant | 2-[[5-[N-methyl-N-(2,2,2-trichloroethoxycarbonyl)aminomethyl]-2furyl]methylthio]ethylamine | HCID 14671749 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-methanesulfonyl-N'-[2-[[5-[N-methyl-N-(2,2,2-trichloroethoxycarbonyl)aminomethyl]-2furyl]methylthio]ethyl]-O-phenylisourea | HCID 19847901 | 78% |
Reaction Steps
11.6 g of diphenyl methanesulfonylimidocarbonate was dissolved in 40 ml of methylene chloride. With ice-cooling, thereto was added 15 g of 2-[[5-[N-methyl-N-(2,2,2-trichloroethoxycarbonyl)aminomethyl]-2furyl]methylthio]ethylamine. The mixture was stirred for 10 minutes. The solvent was removed by distillation under reduced pressure. The residue thus obtained was purified by a column chromatography (eluant: benzene:ethyl acetate=2:1) to obtain 17.8 g (yield: 78%) of oily N-methanesulfonyl-N'-[2-[[5-[N-methyl-N-(2,2,2-trichloroethoxycarbonyl)aminomethyl]-2furyl]methylthio]ethyl]-O-phenylisourea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04871765 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-e0e9d4ffb1b143bd82890815b91456a9 |
| Source note | uspto-grants-1989_10 |