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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1988401생성일: 2026년 10월 27일

m-Chloroperbenzoic acid → N-methyl-4-(2-(methylsulfinyl)benzo[d]oxazol-6-yloxy)picolinamide

https://huagongshe.com/reaction/1988401

반응식

참여 물질

역할이름HCID투입량
반응물m-Chloroperbenzoic acidHCID 70297—
반응물4-(2-(methylthio)benzo[d]oxazol-6-yloxy)-N-methylpyridine-2-carboxamideHCID 57725632—
용매DichloromethaneHCID 6344—
생성물N-methyl-4-(2-(methylsulfinyl)benzo[d]oxazol-6-yloxy)picolinamideHCID 57725414—

반응 단계

To a solution of the 4-(2-(methylthio)benzo[d]oxazol-6-yloxy)-N-methylpyridine-2-carboxamide (1.26 g, 4.0 mmol, 1.0 eq) in 40 mL of methylene chloride was added 3-chloroperoxybenzoic acid (70%, 989 mg, 4.4 mmol, 1.1 eq). The reaction mixture was stirred at room temperature for 5 hours and then was diluted with 200 mL of methylene chloride. The resulting mixture was washed with aqueous sodium bicarbonate and brine then dried over MgSO4, filtered, and evaporated under reduced pressure to give crude product, which was used to next step without further purification. MH+=332.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07553854B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-6322664519874d0588641a8cd9015788
출처 메모uspto-grants-2009_06