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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32290Generated: October 25, 2026

Triethylamine → N-(2-diethylamino-ethyl)-4-(bismethanesulfonylamino)-2-methoxy-benzamide

https://huagongshe.com/reaction/32290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-Amino-N-[2-(diethylamino)ethyl]-2-methoxybenzamideHCID 77374—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
ProductN-(2-diethylamino-ethyl)-4-(bismethanesulfonylamino)-2-methoxy-benzamideHCID 66934940100.1%

Reaction Steps

265 mg (1 mmol) of 4-amino-N-(2-diethylamino-ethyl)-2-methoxy-benzamide is introduced into 15 ml of methylene chloride and mixed in succession with 111 mg (1.1 mmol) of triethylamine and 126 mg (1.1 mmol) of methanesulfonic acid chloride. It is stirred for 2 hours at room temperature and then allowed to stand overnight. It is then mixed with 25 ml of saturated sodium bicarbonate solution and shaken out three times with 25 ml each of methylene chloride. The collected organic phase is dried, filtered and concentrated by evaporation. The residue is chromatographed on 10 g of basic silica gel (Isolute flash Si NH2) with a gradient from cyclohexane:ethyl acetate=100:0 to 50:50. 232 mg (52.6% of theory) of N-(2-diethylamino-ethyl)-4-(bismethanesulfonylamino)-2-methoxy-benzamide with a melting point of 144.1° C. is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07427390B2
Source datasetuspto-grants-2008_09
ORD IDord-557ed9ad4750411aa66c4b927f5247f6
Source noteuspto-grants-2008_09