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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969171Generated: October 25, 2026

N-(1,1-Dimethylethyl)benzenesulfonamide → N-(tert-Butyl)-2-(1-{[1-(4-chlorophenyl)cyclopropyl]carbonyl}-3-hydroxypyrrolidin-3-yl)benzenesulfonamide

https://huagongshe.com/reaction/969171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(1,1-Dimethylethyl)benzenesulfonamideHCID 314059—
Reactant1-{[1-(4-Chlorophenyl)cyclopropyl]carbonyl}pyrrolidin-3-oneHCID 66661646—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
SolventPentaneHCID 8003—
ProductN-(tert-Butyl)-2-(1-{[1-(4-chlorophenyl)cyclopropyl]carbonyl}-3-hydroxypyrrolidin-3-yl)benzenesulfonamideHCID 11627061—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of N-(tert-butyl)benzenesulfonamide (569 mg, 0.00267 mol) in ether (10 mL, 0.1 mol) was added 1.7 M of tert-butyllithium in pentane (4.7 mL) under nitrogen at −78° C. The mixture was stirred at −78° C. for 15 minutes, then at 0° C. for 1 hour. The reaction mixture then was cooled down to −78° C. again and a solution of 1-{[1-(4-chlorophenyl)cyclopropyl]carbonyl}pyrrolidin-3-one (640 mg, 0.0024 mol) in ether was added. After stirring for 2 hours, the reaction mixture was quenched with saturated NH4Cl aqueous solution and then extracted with EtOAc. The combined organic layer was washed with brine, dried over MgSO4 and concentrated. The crude product was purified using Combiflash eluting with 30% AcOEt in hexanes to afford the desired product. LC/MS (M+H+) 478.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07304081B2
Source datasetuspto-grants-2007_12
ORD IDord-9f7613bc242f480d9e7617c2400fa505
Source noteuspto-grants-2007_12