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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81674Generated: October 29, 2026

Dimethylformamide → 5,6-Dichloro-N-[2-(dimethylamino)ethyl]-N-methylnicotinamide

https://huagongshe.com/reaction/81674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantThionyl ChlorideHCID 24386—
Reactant1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
ReactantHCID 178524771HCID 178524771—
SolventWaterHCID 962—
Product5,6-Dichloro-N-[2-(dimethylamino)ethyl]-N-methylnicotinamideHCID 63692912100%

Reaction Conditions

Temperature90 °C

Reaction Steps

N,N-dimethylformamide (0.05 ml, 0.65 mmol) was added to a thionyl chloride solution (10 ml) of 5-chloro-6-hydroxynicotinic acid (1.0 g, 5.76 mmol), and stirred under a nitrogen atmosphere at 90° C. for 1 hour. The reaction solution was concentrated under reduced pressure, and with cooling with ice, N,N,N′-trimethylethane-1,2-diamine (2.32 ml, 17.3 mmol) was added to an N,N-dimethylformamide solution (10 ml) of the obtained residue, and stirred at room temperature for 3 minutes. Saturated saline water was added to the reaction solution, extracted with chloroform, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by amine-type silica gel column chromatography (Biotage NH, hexane:ethyl acetate=4:1 go 1:1) to obtain 5,6-dichloro-N-[2-(dimethylamino)ethyl]-N-methylnicotinamide (1.59 g, yield: 100%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846700B2
Source datasetuspto-grants-2014_09
ORD IDord-7f1e1229ed934e3b887e9910b557e00e
Source noteuspto-grants-2014_09