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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116530Generated: October 31, 2026

Diisopropylethylamine → 3-Phenylsulfonyl-8-piperazin-1-yl-quinoline hydrochloride

https://huagongshe.com/reaction/2116530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Chloroethyl chloroformateHCID 521305—
ReactantHCID 69198975HCID 69198975—
Solvent1,2-DichloroethaneHCID 11—
Product3-Phenylsulfonyl-8-piperazin-1-yl-quinoline hydrochlorideHCID 5697214152.5%

Reaction Steps

A stirred solution of 8-(4-methyl-piperazin-1-yl)-3-phenylsulfonylquinoline hydrochloride (D10) (0.148 g, 0.4 mmol), 1-chloroethyl chloroformate (0.093 ml, 0.85 mmol) and N,N-diisopropylethylamine (0.148 ml, 0.85 mmol) in 1,2-dichloroethane (9 ml) was heated at reflux for 1.25 h under argon. The reaction mixture was cooled to ambient temperature and concentrated in vacuo to an oil. The oil was purified by chromatography over silica gel eluting with a gradient of methanol/dichloromethane, pooling fractions which contained the major component (Rf 0.9, methanol/dichloromethane 1:19). The purified material was redissolved in methanol (15 ml) and the solution was refluxed for 1 h under argon. The reaction mixture was cooled to ambient temperature and concentrated in vacuo to a solid which was stirred with diethyl ether (5 ml) and filtered to afford the title compound (D11) (0.08 g, 0.21 mmol, 51%);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439244B2
Source datasetuspto-grants-2008_10
ORD IDord-1ea7b831b4ce4031b4a47fb6fc36be36
Source noteuspto-grants-2008_10