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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15333생성일: 2026년 10월 26일

8-Bromo-2,3-dihydro-1,4-benzodioxine-6-carbaldehyde → Racemic methyl 2-[3-fluoro-6-(methyloxy)-1,5-naphthyridin-4-yl]-3-[(cis)-3-fluoro-4-({[(phenylmethyl)oxy]carbonyl}amino)-1-piperidinyl]propanoate

https://huagongshe.com/reaction/15333

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참여 물질

역할이름HCID투입량
반응물8-Bromo-2,3-dihydro-1,4-benzodioxine-6-carbaldehydeHCID 16637176—
반응물Furo[2,3-c]pyridin-5-ylmethanolHCID 22047174—
반응물Methyl 2-[3-fluoro-6-(methyloxy)-1,5-naphthyridin-4-yl]-2-propenoateHCID 57486873—
반응물benzyl N-[(3R,4S)-3-fluoropiperidin-4-yl]carbamateHCID 68566554—
촉매1,1,3,3-TetramethylguanidineHCID 66460—
용매DimethylformamideHCID 6228—
생성물Racemic methyl 2-[3-fluoro-6-(methyloxy)-1,5-naphthyridin-4-yl]-3-[(cis)-3-fluoro-4-({[(phenylmethyl)oxy]carbonyl}amino)-1-piperidinyl]propanoateHCID 68685415100%

반응 조건

온도80 °C

반응 단계

A solution of methyl 2-[3-fluoro-6-(methyloxy)-1,5-naphthyridin-4-yl]-2-propenoate (953 mg, 3.63 mmol), cis-phenylmethyl[3-fluoro-4-piperidinyl]carbamate Enantiomer 2 (for a synthesis see WO2004058144, prepared by analogy to Examples 142(b), (c) and (d) from the Enantiomer 2 of Example 142(a)) (1.1 g, 4.35 mmol) and 1,1,3,3-tetramethylguanidine (6 drops) in DMF (3.5 ml) was heated at 80° C. under argon for 3 hours, cooled and evaporated. Chromatography, eluting with 1% methanol/dichloromethane, gave the product in 100% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732461B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-721d8cceaacc48fea2c0ccf5e6db4a4c
출처 메모uspto-grants-2010_06