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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013429Generated: October 30, 2026

4-Toluenesulfonyl chloride → Toluene-4-sulfonic acid 1-benzyl-4-(4-bromo-thiophen-2-yl)-pyrrolidine-3-yl-methyl ester

https://huagongshe.com/reaction/1013429

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Amino-3,4-dimethylpyridineHCID 11007884—
Reactant[1-Benzyl-4-(4-bromo-thiophen-2-yl)-pyrrolidin-3-yl]-methanolHCID 58624942—
SolventDichloromethaneHCID 6344—
ProductToluene-4-sulfonic acid 1-benzyl-4-(4-bromo-thiophen-2-yl)-pyrrolidine-3-yl-methyl esterHCID 5862493051%

Reaction Steps

Diisopropylethylamine (20.2 g, 0.156 mol), dimethyl aminopyridine (320 mg, 2.6 mmol) and TsCl were (9.88 g, 0.052 mol) were added, respectively, to the product of step b) (9.1 g, 0.026 mol) in 150 mL of dichloromethane at 0° C. The reaction mixture was stirred overnight at room temperature and then was quenched with 75 mL of 1 M HCl and extracted with dichloromethane (3×100 mL). The combined organic extracts were washed with brine (100 mL), dried with MgSO4 and evaporated in vacuo to give the crude product that was purified by column chromatography (SiO2) using a 0-50% methanol-dichloromethane gradient to give the subtitle compound (6.7 g, yield: 51%). MS calculated for C23H24BrNO3S2 +H: 506, observed: 506 and 508.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981919B2
Source datasetuspto-grants-2011_07
ORD IDord-c59eb45c93e34ec78b0aeee85895ce8a
Source noteuspto-grants-2011_07