HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azetidine → Benzyl (azetidin-1-ylsulfonyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azetidine | HCID 10422 | — |
| Reactant | HCID 178482961 | HCID 178482961 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl (azetidin-1-ylsulfonyl)carbamate | HCID 89633251 | 1,102.5% |
Reaction Steps
Azetidine (0.36 g, 0.5 mmol) was added to N-{1-[N-(benzyloxycarbonyl)-sulfamoyl]pyridin-4(1H)-ylidene}-N-methylmethanaminium chloride (Preparation 21, 2.0 g, 0.5 mmol) in DCM (10 mL). The reaction mixture was stirred overnight at room temperature. The mixture was concentrated in vacuo and the residue partitioned between ethyl acetate (50 mL) and water (50 mL). The organic layer was discarded and the aqueous layer was acidified with 1M HCl. The aqueous layer was extracted with ethylacetate (2×50 mL), dried over magnesium sulfate and concentrated to afford the title compound (1.49 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09085517B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-9aaf321f7d2f4962a86df03130dc5cc3 |
| Source note | uspto-grants-2015_07 |