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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734973Generated: October 27, 2026

Triethylamine → N-[5-(3-{4-[(2-methylpropyl)sulfonyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamide

https://huagongshe.com/reaction/734973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSulfuryl chlorideHCID 24648—
Reactant1-Propanesulfonyl chloride, 2-methyl-HCID 182236—
ReactantN-{5-[3-(1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamideHCID 57843497—
SolventDichloromethaneHCID 6344—
ProductN-[5-(3-{4-[(2-methylpropyl)sulfonyl]-1-piperazinyl}-6-quinoxalinyl)-3-pyridinyl]benzenesulfonamideHCID 5784339320%

Reaction Steps

To a solution of N-{5-[3-(1-piperazinyl)-6-quinoxalinyl]-3-pyridinyl}benzenesulfonamide (0.20 mmol) and triethylamine (0.20 mmol) in dichloromethane (2 ml) was added a sulfonyl chloride such as 2-methyl-1-propanesulfonyl chloride (0.22 mmol). The reaction stirred for 18 hours at ambient temperature and purified on silica by column chromatography (80% ethyl acetate/hexanes). The desired fractions were combined and concentrated to give the title compound (22 mg, 20%) as an off-white solid. MS(ES)+ m/e 567.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592342B2
Source datasetuspto-grants-2009_09
ORD IDord-e54585a1fdf44512b5607e9217bb1aa0
Source noteuspto-grants-2009_09