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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930192Generated: November 1, 2026

1-Naphthalenesulfonyl chloride → HCID 86603239, compound

https://huagongshe.com/reaction/1930192

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Naphthalenesulfonyl chlorideHCID 66560—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 21994163HCID 21994163—
SolventDichloromethaneHCID 6344—
ProductHCID 86603239HCID 8660323972%

Reaction Steps

A solution of 2-(4-aminobutyl)-1,2,3,4-tetrahydroisoquinoline dihydrochloride (272 mg, 1 mmol), N,N-diisopropylethylamine (517 mg, 4 mmol) in CH2Cl2 (10 mL), was added naphtalene-1-sulfonyl chloride (238 mg, 1.05 mmol) and was stirred overnight at room temperature. The resulting solution was washed with water (3×15 mL) and dried over Na2SO4, and evaporated to dryness. The free base was dissolved in 2-propanol (5 mL). A 2.8 M solution of hydrogen chloride in ethanol (0.40 mL) was then added. The product was crystallized and collected by filtration, and vacuum dried to give a white solid (310 mg, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188115B2
Source datasetuspto-grants-2012_05
ORD IDord-dcc4e43f6a9c47e3a909b9b18a9aa534
Source noteuspto-grants-2012_05