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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304272Generated: November 3, 2026

Triethylamine → 7-methoxy-3,4-dihydro-1H-isoquinoline-2-sulfonyl chloride

https://huagongshe.com/reaction/2304272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSulfuryl chlorideHCID 24648—
Reactant7-Methoxy-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 2752197—
SolventChloroformHCID 6212—
Product7-methoxy-3,4-dihydro-1H-isoquinoline-2-sulfonyl chlorideHCID 22665676—

Reaction Steps

To a stirred, precooled solution (−40° C.) of 0.41 mL of sulfuryl chloride in 10 mL of chloroform was added a mixture of 1.0 g of 7-methoxy-1,2,3,4-tetrahydro-isoquinoline-hydrochloride and 2.1 mL of triethylamine in 25 mL of chloroform at 40° C. Stirring was continued at −30° C. for one hour and additionally at 5° C. for one hour. The mixture was poured on ice, the organic layer extracted with cold water, dried (sodium sulfate) and concentrated. The residue was redissolved in diethyl ether and chromatographed on silica gel (isohexane/ethyl acetate=8/2 v/v) yielding 0.62 g of 7-methoxy-3,4-dihydro-1H-isoquinoline-2-sulfonyl chloride as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432955B1
Source datasetuspto-grants-2002_08
ORD IDord-a45b7351ec7447569f1413949c097629
Source noteuspto-grants-2002_08