HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1,1-Dimethylethyl 4-[1-(diphenylmethyl)-3-azetidinyl]hexahydro-1H-1,4-diazepine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(Diphenylmethyl)azetidin-3-yl methanesulfonate | HCID 2758716 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Product | 1,1-Dimethylethyl 4-[1-(diphenylmethyl)-3-azetidinyl]hexahydro-1H-1,4-diazepine-1-carboxylate | HCID 21183762 | — |
Reaction Steps
To a solution of 1-diphenylmethyl-3-methanesulphonyloxyazetidine (WO 96/05193) (25 g) in acetonitrile (800 mL) were added the compound of PREPARATION 24 (19 g) and potassium carbonate (33 g). The reaction mixture was heated to reflux for 12 h, then cooled to room temperature. Water was added to the resulting slurry, and the mixture extracted three times with ethyl acetate. 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 dichloromethane:methanol (95:5) yielded the title compound (24.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06262046B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-56965c0a85c7480881ad8a711f4fef68 |
| Source note | uspto-grants-2001_07 |