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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1525671Generated: November 3, 2026

Azetidine → Benzyl (azetidin-1-ylsulfonyl)carbamate

https://huagongshe.com/reaction/1525671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzetidineHCID 10422—
ReactantHCID 178482961HCID 178482961—
SolventDichloromethaneHCID 6344—
ProductBenzyl (azetidin-1-ylsulfonyl)carbamateHCID 896332511,102.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085517B2
Source datasetuspto-grants-2015_07
ORD IDord-9aaf321f7d2f4962a86df03130dc5cc3
Source noteuspto-grants-2015_07