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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 655324생성일: 2026년 10월 24일

Triphenylphosphine → 5-methyl-3-[3-(5-methylpyrimidin-2-yl)benzyl]-3H-benzoxazol-2-one

https://huagongshe.com/ko/reaction/655324

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물5-Methyloxazolo[4,5-b]pyridin-2(3H)-oneHCID 10012075—
반응물[3-(5-Methylpyrimidin-2-yl)phenyl]methanolHCID 59484945—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물5-methyl-3-[3-(5-methylpyrimidin-2-yl)benzyl]-3H-benzoxazol-2-oneHCID 25125095—

반응 조건

온도0 °C

반응 단계

112 mg (0.75 mmol) of 5-methyl-3H-oxazolo[4,5-b]pyridin-2-one, 180 mg (0.90 mmol) of [3-(5-methylpyrimidin-2-yl)phenyl]methanol and 238 mg (0.90 mmol) of triphenylphosphine are suspended in 5 ml of THF, and the mixture is stirred for 30 min. The mixture is subsequently cooled to 0° C., and 186 μl (0.90 mmol) of diisopropyl azodicarboxylate are added. The reaction mixture is stirred at room temperature for 2 h. The reaction mixture is diluted with 20 ml of dichloromethane, washed with 2×20 ml of water, dried over sodium sulfate and evaporated. The residue is purified by column chromatography on silica gel; yield: 101 mg of “A45”; ESI: 332 (M+H); Rt=4.91 min (method C);

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08071593B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-4e4fbdd9c9a34a518667459884621da4
출처 메모uspto-grants-2011_12