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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2370513생성일: 2026년 10월 24일

m-Chloroperbenzoic acid → 2-Pyridinecarboxamide, N-methyl-4-[[2-(methylsulfinyl)-6-benzothiazolyl]oxy]-

https://huagongshe.com/ko/reaction/2370513

반응식

참여 물질

역할이름HCID투입량
반응물m-Chloroperbenzoic acidHCID 70297—
반응물Sodium BicarbonateHCID 516892—
반응물N-Methyl-4-((2-(methylthio)benzo[d]thiazol-6-yl)oxy)picolinamideHCID 57725401—
용매DichloromethaneHCID 6344—
생성물2-Pyridinecarboxamide, N-methyl-4-[[2-(methylsulfinyl)-6-benzothiazolyl]oxy]-HCID 57725393—

반응 단계

To the solution of 4-(2-methylsulfanyl-benzothiazol-6-yloxy)-pyridine-2-carboxylic acid methylamide from step 3 (3.88 g, 11.72 mmol, 1.0 eq) in DCM (20 mL) at 0° C., was added MCPBA (77%, 2.88 g, 1.1 eq). The mixture was stirred at this temperature for one hour. Saturated sodium bicarbonate solution (100 mL) was added. The aqueous layer was extracted with DCM (3×150 mL). The organic layer was dried over sodium sulfate, filtered, and evaporated in vacuo to yield 4-(2-methanesulfinyl-benzothiazol-6-yloxy)-pyridine-2-carboxylic acid methylamide as white powder in quantitative yields. The crude product was used in the next step without purification. M+H=348.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08710048B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-bc512e3c69a84843a9eef4cf67443585
출처 메모uspto-grants-2014_04