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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30299Generated: October 26, 2026

4-Toluenesulfonyl chloride → HCID 58624930, compound

https://huagongshe.com/reaction/30299

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—
ProductHCID 58624930HCID 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 numberUS07423056B2
Source datasetuspto-grants-2008_09
ORD IDord-8520b01f0f8f4282b49df7634b7e7b63
Source noteuspto-grants-2008_09