HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexyl isocyanate → 3-[2-(trifluoromethyl)-4'-(methylthio)benzhydryloxy]-N-(cyclo-hexyl)azetidine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexyl isocyanate | HCID 18502 | — |
| Reactant | Carbonate Ion | HCID 19660 | — |
| Reactant | 3-[2-Trifluoromethyl-4'-(methylthio)benzhydryloxy]azetidine hydrochloride | HCID 68904236 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[2-(trifluoromethyl)-4'-(methylthio)benzhydryloxy]-N-(cyclo-hexyl)azetidine-1-carboxamide | HCID 11282986 | — |
Reaction Steps
To a solution of 3-[2-(trifluoromethyl)-4′-(methylthio)benzhydryloxy]azetidine hydrochloride (118) (100 mg, 0.26 mmol) in anhydrous DCM (5 mL) was added MP-carbonate (3.10 mmol/g; 250 mg, 0.84 mmol) and cyclohexyl isocyanate (33 μL, 0.26 mmol). The resultant mixture was shaken at ambient temperature for 16 h, after which time it was poured onto a DCM-wetted SCX-2 (1 g) cartridge. The sample was eluted with DCM (18 mL), then evaporated to afford the desired product as a white, crystalline solid (65 mg, 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07504522B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-b882c3fe42704152805daba2a81e1922 |
| Source note | uspto-grants-2009_03 |