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HRID 51845作成日:2026年10月27日

4-(Chloromethyl)benzoyl chloride → 4-chloromethyl-N-{4-methoxy-7-[(2-methoxy-ethyl)-methyl-amino]-benzothiazol-2-yl}-benzamide

https://huagongshe.com/reaction/51845

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Chloromethyl)benzoyl chlorideHCID 70136—
反応物DiisopropylethylamineHCID 81531—
反応物4-methoxy-N7-(2-methoxy-ethyl)-N7-methyl-benzothiazole-2,7-diamineHCID 22015744—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物4-chloromethyl-N-{4-methoxy-7-[(2-methoxy-ethyl)-methyl-amino]-benzothiazol-2-yl}-benzamideHCID 1021648742.5%

反応手順

To a stirred solution of 300 mg (1.12 mmol) 4-methoxy-N7-(2-methoxy-ethyl)-N7-methyl-benzothiazole-2,7-diamine and 1.12 ml (6.56 mmol) N-ethyldiisopropylamine in 10 ml THF at room temperature was added dropwise a solution of 257 mg (1.36 mmol) 4-(chloromethyl)-benzoyl chloride in 3 ml dichloromethane and stirring continued at room temperature for 16 h. The reaction mixture was then concentrated in vacuo. Flash chromatography (1/1 ethyl acetate/hexane) followed by trituration in ether and hexane afforded 200 mg (42%) 4-chloromethyl-N-{4-methoxy-7-[(2-methoxy-ethyl)-methyl-amino]-benzothiazol-2-yl}-benzamide as a light yellow crystalline solid. ES-MS m/e (%): 422 (M{37Cl}+H+, 32), 420 (M{35Cl}+H+, 100).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713499B2
出典データセットuspto-grants-2004_03
ORD IDord-5d5ede813284486dbafb3c5d5c933bb6
出典メモuspto-grants-2004_03