HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-Diphenylmethyl-3-(N-methyl benzenesulphonamido)azetidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | N-Methylbenzenesulfonamide | HCID 78858 | — |
| Reactant | 1-(Diphenylmethyl)azetidin-3-yl methanesulfonate | HCID 2758716 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-Diphenylmethyl-3-(N-methyl benzenesulphonamido)azetidine | HCID 21183795 | 75.7% |
Reaction Steps
To a solution of 1-diphenylmethyl-3-methanesulphonyloxyazetidine (WO 96/05193) (1.4 g) in dioxane (25 mL) were added N-methyl benzenesulphonamide (1.2 g) and caesium carbonate (2.6 g). The reaction mixture was heated to reflux for 3 h, then cooled to room temperature. Water (20 mL) was added to the resulting slurry, and the mixture was extracted with ethyl acetate (3×25 mL). The combined organics were washed with brine, dried over magnesium sulphate, filtered and dried in vacuo to yield crude product. Chromatography on silica gel eluting with ethyl acetate:hexanes (2:3 by volume) yielded the title compound as a white foam (1.31 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06262046B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-6102f2a111f243de9734956b68074544 |
| Source note | uspto-grants-2001_07 |