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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51845생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/51845

반응식

참여 물질

역할이름HCID투입량
반응물4-(Chloromethyl)benzoyl chlorideHCID 70136—
반응물DiisopropylethylamineHCID 81531—
반응물4-methoxy-N7-(2-methoxy-ethyl)-N7-methyl-benzothiazole-2,7-diamineHCID 22015744—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물4-chloromethyl-N-{4-methoxy-7-[(2-methoxy-ethyl)-methyl-amino]-benzothiazol-2-yl}-benzamideHCID 1021648742.5%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713499B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-5d5ede813284486dbafb3c5d5c933bb6
출처 메모uspto-grants-2004_03