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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 32290Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/32290

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt4-Amino-N-[2-(diethylamino)ethyl]-2-methoxybenzamideHCID 77374—
EduktSodium BicarbonateHCID 516892—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(2-diethylamino-ethyl)-4-(bismethanesulfonylamino)-2-methoxy-benzamideHCID 66934940100,1%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07427390B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-557ed9ad4750411aa66c4b927f5247f6
Quellennotizuspto-grants-2008_09