戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2262353作成日:2026年10月25日

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

https://huagongshe.com/reaction/2262353

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methanesulfonyl chlorideHCID 31297—
反応物4-Amino-N-[2-(diethylamino)ethyl]-2-methoxybenzamideHCID 77374—
反応物Sodium BicarbonateHCID 516892—
溶媒DichloromethaneHCID 6344—
生成物N-(2-diethylamino-ethyl)-4-(bismethanesulfonylamino)-2-methoxy-benzamideHCID 66934940100.1%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07850948B2
出典データセットuspto-grants-2010_12
ORD IDord-d7db9b057cd24ffa91942e1dcf43f602
出典メモuspto-grants-2010_12