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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 276787생성일: 2026년 10월 26일

4-ethoxymethylene-2-(1)-naphthyl-5(4H)-oxazolone → 4-{4-[(benzylidene-amino)-methyl]-piperidin-1-ylmethylene}-2-naphthalen-1-yl-4H-oxazol-5-one

https://huagongshe.com/reaction/276787

반응식

참여 물질

역할이름HCID투입량
반응물4-ethoxymethylene-2-(1)-naphthyl-5(4H)-oxazoloneHCID 356930—
반응물N-Benzylidene(piperidin-4-yl)methanamineHCID 11820173—
용매TetrahydrofuranHCID 8028—
생성물4-{4-[(benzylidene-amino)-methyl]-piperidin-1-ylmethylene}-2-naphthalen-1-yl-4H-oxazol-5-oneHCID 54057694—

반응 단계

To a solution of 4-ethoxymethylene-2-naphthalen-1-yl-4H-oxazol-5-one (11.40 g, 43 mmol) in tetrahydrofuran, benzylidene-piperidin-4-ylmethyl-amine (8.60 g, 43 mmol) was added, and the mixture was stirred at room temperature for 24 h. The reaction mixture was concentrated under reduced pressure to yield 4-{4-[(benzylidene-amino)-methyl]-piperidin-1-ylmethylene}-2-naphthalen-1-yl-4H-oxazol-5-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06355641B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-0ea03cc5fb7f4f1cb7f181c2ebd1448a
출처 메모uspto-grants-2002_03