Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809035Generated: October 30, 2026

2-Nitrobenzenesulfonyl chloride → HCID 67051720, compound

https://huagongshe.com/reaction/1809035

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitrobenzenesulfonyl chlorideHCID 15540—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 67051836HCID 67051836—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67051720HCID 6705172079.5%

Reaction Steps

To a solution of 1,1-dimethylethyl 3-hydroxy-3-piperazin-2-ylazetidine-1-carboxylate (227 mg, 0.88 mmol) and N,N-diisopropylethylamine (436 μL, 2.64 mmol) in THF (5 mL) was added 2-nitrobenzenesulfonyl chloride (195 mg, 0.88 mmol). The mixture was stirred at room temperature for 2 hours. The solution was concentrated and the residue was purified by column chromatography (95% dichloromethane: 5% methanol) to provide 1,1-dimethylethyl 3-hydroxy-3-{4-[(2-nitrophenyl)sulfonyl]piperazin-2-yl}azetidine-1-carboxylate as a white foam (308 mg, 0.70 mmol, 79% yield). 1H NMR (400 MHz, CDCl3): 7.98 (m, 1H), 7.72 (m, 2H), 7.64 (m, 1H), 3.96 (d, 1H), 3.94 (d, 1H), 3.85 (d, 1H), 3.79 (d, 1H), 3.79-3.73 (m, 2H), 3.11 (m, 1H), 3.05 (dd, 1H), 3.00 (br s, 1H), 2.94 (dt, 1H), 2.78 (dt, 1H), 2.68 (dd, 1H), 1.45 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362002B2
Source datasetuspto-grants-2013_01
ORD IDord-36767c461d934debb40923cdd52326b1
Source noteuspto-grants-2013_01