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HRID 2180394作成日:2026年10月26日

1-Naphthalenemethanamine → 3-{3-[(Naphthalen-1-ylmethyl)-sulfamoyl]-phenyl}-acrylic acid methyl ester

https://huagongshe.com/reaction/2180394

反応式

関与物質

役割名称HCID仕込み量
反応物1-NaphthalenemethanamineHCID 8355—
反応物Sodium BicarbonateHCID 516892—
反応物3-(3-Chlorosulfonylphenyl)acrylic acid methyl esterHCID 73708742—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物3-{3-[(Naphthalen-1-ylmethyl)-sulfamoyl]-phenyl}-acrylic acid methyl esterHCID 6701954076%

反応手順

A solution of 3-(3-chlorosulfonylphenyl)acrylic acid methyl ester (3) (0.4 g, 1.53 mmol) in dioxane (5 ml) was added to a mixture of 1-naphthalenemethylamine (0.24 g, 1.53 mmol) in dioxane (1 ml) and NaHCO3 (0.25 g, 3.06 mmol) in water (3 ml), and the resultant solution was stirred at room temperature until the completion of the reaction (control by TLC). The reaction mixture was evaporated and the residue was partitioned between ethyl acetate and 2N HCl. The organic layer was washed successively with water, saturated NaCl, and dried (Na2SO4). The solvent was removed and the residue was chromatographed on silica gel with petroleum ether-ethyl acetate (2:1, v/v) as eluent. The obtained product was washed with diethyl ether to give the title compound (0.44 g, 76%) as a white solid. 1H NMR (DMSO-d6, HMDSO), δ: 3.74 (3H, s); 4.47 (2H, d, J=6.0 Hz); 6.69 (1H, d, J=16.0 Hz); 7.32-8.32 (13H, m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06888027B2
出典データセットuspto-grants-2005_05
ORD IDord-0ae0692d132f42afbf7e917c64fac0e3
出典メモuspto-grants-2005_05