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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81672Generated: October 25, 2026

Tetrahydrofuran → 5,6-dichloro-N-[3-(dimethylamino)propyl]-N-methylpyridine-3-sulfonamide

https://huagongshe.com/reaction/81672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant1,3-Propanediamine, N1,N1,N3-trimethyl-HCID 78302—
Reactant5,6-dichloropyridine-3-sulfonyl ChlorideHCID 4736911—
SolventWaterHCID 962—
Product5,6-dichloro-N-[3-(dimethylamino)propyl]-N-methylpyridine-3-sulfonamideHCID 6460880469%

Reaction Steps

With cooling with ice, triethylamine (0.57 ml, 4.06 mmol) and N,N,N′-trimethylpropane-1,3-diamine (0.34 ml, 2.23 mmol) were added to a tetrahydrofuran solution (5 ml) of 5,6-dichloropyridin-3-sulfonyl chloride (500 mg, 2.03 mmol), and stirred for 5 minutes. Saturated saline water was added to the reaction solution, extracted with chloroform, and the organic layer was dried over anhydrous sodium sulfate, concentrated under reduced pressure. The obtained residue was purified by amine-type silica gel column chromatography (Biotage NH, hexane:ethyl acetate=6:1 to 4:1) to obtain 5,6-dichloro-N-[3-(dimethylamino)propyl]-N-methylpyridine-3-sulfonamide (454 mg, yield: 69%) as a red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846700B2
Source datasetuspto-grants-2014_09
ORD IDord-30d413919aa64b44b3d9134595c4c0ad
Source noteuspto-grants-2014_09