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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 455186생성일: 2026년 10월 24일

Dimethylformamide → N-(3-{[2-(acetylamino)-7-cyano-1,3-benzothiazol-6-yl]oxy}phenyl)-4-chloro-3-(1-cyano-1-methylethyl)benzamide

https://huagongshe.com/ko/reaction/455186

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Oxalyl chlorideHCID 65578—
반응물4-Chloro-3-(1-cyano-1-methylethyl)benzoic acidHCID 66810425—
반응물N-[6-(3-aminophenoxy)-7-cyano-1,3-benzothiazol-2-yl]acetamideHCID 86644686—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물N-(3-{[2-(acetylamino)-7-cyano-1,3-benzothiazol-6-yl]oxy}phenyl)-4-chloro-3-(1-cyano-1-methylethyl)benzamideHCID 5945449166.2%

반응 단계

To a solution of 4-chloro-3-(1-cyano-1-methylethyl)benzoic acid (83 mg, 0.370 mmol) in tetrahydrofuran (2 mL) were added oxalyl chloride (40 μL, 0.462 mmol) and N,N-dimethylformamide (5 μL), and the mixture was stirred at room temperature for 1 hr. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in N,N-dimethylacetamide (2 mL). N-[6-(3-Aminophenoxy)-7-cyano-1,3-benzothiazol-2-yl]acetamide (100 mg, 0.308 mmol) produced in Example 12(ii) was added to the solution, and the mixture was stirred at room temperature for 10 hr. The reaction mixture was diluted with ethyl acetate (10 mL), washed successively with 5% aqueous sodium hydrogen carbonate solution (5 mL) and saturated brine (5 mL), and dried over anhydrous sodium sulfate. Insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was crystallized from ethyl acetate to give the title compound (108 mg, 66%) as a white powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08497274B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-7959f218305344da910aeb0200fa7e60
출처 메모uspto-grants-2013_07