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HRID 226137作成日:2026年10月25日

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

https://huagongshe.com/reaction/226137

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 NaCl1 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US07557140B2
出典データセットuspto-grants-2009_07
ORD IDord-ce6780fef75c4923a829dacb12c62c8f
出典メモuspto-grants-2009_07