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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 655338생성일: 2026년 10월 24일

Triphenylphosphine → 5-methyl-3-{3-[5-(4-methylpiperazin-1-yl)pyrimidin-2-yl]benzyl}-3H-oxazolo[4,5-b]pyridin-2-one

https://huagongshe.com/ko/reaction/655338

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Di-tert-butyl azodicarboxylateHCID 97268—
반응물5-Methyloxazolo[4,5-b]pyridin-2(3H)-oneHCID 10012075—
반응물{3-[5-(4-Methylpiperazin-1-yl)pyrimidin-2-yl]phenyl}methanolHCID 59484860—
용매DimethylformamideHCID 6228—
생성물5-methyl-3-{3-[5-(4-methylpiperazin-1-yl)pyrimidin-2-yl]benzyl}-3H-oxazolo[4,5-b]pyridin-2-oneHCID 58486104—

반응 단계

67 mg (0.44 mmol) of 5-methyl-3H-oxazolo[4,5-b]pyridin-2-one and 125 mg (0.44 mmol) of {3-[5-(4-methylpiperazin-1-yl)pyrimidin-2-yl]phenyl}methanol are suspended in 5 ml of DMF with 222 mg (0.67 mmol) of polymer-bound triphenylphosphine (about 3 mmol of triphenylphosphine per g), and the mixture is shaken at room temperature for 30 min. 156 mg (0.67 mmol) of di-tert-butyl azodicarboxylate are added. The reaction mixture is shaken at room temperature for 15 h. The reaction mixture is filtered, the residue is evaporated, and the residue is purified by column chromatography on silica gel, giving 67 mg of “A125”; HPLC: Rt=2.26 min (method B); ESI: 418 (M+H);

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08071593B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-51384a395767447e990e66c19e294b6d
출처 메모uspto-grants-2011_12