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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1943138생성일: 2026년 10월 25일

4-(N-Boc-amino)piperidine → 1,1-Dimethylethyl (1-{2-hydroxy-3-[7-(methyloxy)-2-oxo-3,4-dihydro-1,8-naphthyridin-1(2H)-yl]propyl}-4-piperidinyl)carbamate

https://huagongshe.com/reaction/1943138

반응식

참여 물질

역할이름HCID투입량
반응물4-(N-Boc-amino)piperidineHCID 723833—
반응물7-(Methyloxy)-1-(2-oxiranylmethyl)-3,4-dihydro-1,8-naphthyridin-2(1H)-oneHCID 86642091—
용매DimethylformamideHCID 6228—
생성물1,1-Dimethylethyl (1-{2-hydroxy-3-[7-(methyloxy)-2-oxo-3,4-dihydro-1,8-naphthyridin-1(2H)-yl]propyl}-4-piperidinyl)carbamateHCID 6904655638%

반응 단계

A solution of 7-(methyloxy)-1-(2-oxiranylmethyl)-3,4-dihydro-1,8-naphthyridin-2(1H)-one (428 mg, 1.829 mmol) and 1,1-dimethylethyl 4-piperidinylcarbamate (366 mg, 1.829 mmol) in DMF (2 ml) under argon was heated at 120° C. for 1 h. The mixture was then evaporated and chromatographed (0-10% methanol/DCM) to give the product as a yellow oil (301 mg, 38%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08389524B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-4bb6652f8eb747718ddb08b5f1599f4b
출처 메모uspto-grants-2013_03