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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1041867Generated: October 26, 2026

Dimethylamine, hydrochloride → 4-Dimethylamino-3-methanesulfonyl-benzoic acid methyl ester

https://huagongshe.com/reaction/1041867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-Fluoro-3-(methylsulfonyl)benzoateHCID 10752025—
SolventDimethyl SulfoxideHCID 679—
Product4-Dimethylamino-3-methanesulfonyl-benzoic acid methyl esterHCID 6690912456%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of 5.23 g (22.5 mmol) 4-Fluoro-3-methanesulfonyl-benzoic acid methyl ester (J. Med. Chem.; 40; 13; 1997; 2017-2034) and 60.0 ml dimethylsulphoxid were added 2.23 g (27.0 mmol) dimethylamine hydrochloride and 6.54 g (47.3 mmol) potassium carbonate. The reaction mixture was stirred for 7 h at 60° C. in an autoclave and was concentrated with high vacuum rotation evaporator at 65° C. The residue was diluted with dichloromethane, washed twice with water. The combined water phases were extracted with dichloromethane. The combined dichloromethane phases were washed with diluted sodium hydrogen carbonate solution, dried with sodium sulphate and concentrated. The oily crude was purified by column chromatography and the desired product 10a was obtained in 56% yield (3.24 g, 12.6 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557776B2
Source datasetuspto-grants-2013_10
ORD IDord-4e90e05250034a908ee44c51913f701b
Source noteuspto-grants-2013_10