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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51844생성일: 2026년 10월 26일

Hydrochloric Acid → 4-fluoro-N-{4-methoxy-7-[(2-methoxy-ethyl)-methyl-amino]-benzothiazol-2-yl}-benzamide

https://huagongshe.com/reaction/51844

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-Fluorobenzoic AcidHCID 9973—
반응물DiisopropylethylamineHCID 81531—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물4-methoxy-N7-(2-methoxy-ethyl)-N7-methyl-benzothiazole-2,7-diamineHCID 22015744—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
용매1,4-DioxaneHCID 31275—
생성물4-fluoro-N-{4-methoxy-7-[(2-methoxy-ethyl)-methyl-amino]-benzothiazol-2-yl}-benzamideHCID 1012655325.2%

반응 단계

To a stirred solution of 79 mg (0.56 mmol) 4-fluoro-benzoic acid in 10 ml THF were added 235 mg (0.62 mmol) HATU and 0.11 ml (0.62 mmol) N-ethyldiisopropylamine and stirring continued at room temperature for 1 h. A solution of 150 mg (0.56 mmol) 4-methoxy-N7-(2-methoxy-ethyl)-N7-methyl-benzothiazole-2,7-diamine in 5 ml dioxane and 1 ml DMF was then added and stirring continued at room temperature for 16 h. The reaction mixture was then poured into 100 ml 1 M hydrochloric acid and extracted three times with dichloromethane. The combined organic phases were dried over sodium sulfate and concentrated in vacuo. Flash chromatography (1/4-1/1 ethyl acetate/hexane) followed by trituration in hexane afforded 55 mg (25%) 4-fluoro-N-{4-methoxy-7-[(2-methoxy-ethyl)-methyl-amino]-benzothiazol-2-yl}-benzamide as an off-white crystalline solid. ES-MS m/e (%): 390 (M+H+, 100).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713499B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-6413f97c041a4449bed82926c1d1bab4
출처 메모uspto-grants-2004_03