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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2120239생성일: 2026년 10월 24일

Piperidine → HCID 54352759, 화합물

https://huagongshe.com/ko/reaction/2120239

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물4-(2-Hydroxyethyl)indolin-2-oneHCID 10943004—
반응물4-Methoxy-3-(thiophen-2-yl)benzaldehydeHCID 21981024—
용매EthanolHCID 702—
생성물HCID 54352759HCID 5435275947%

반응 단계

A mixture of 4-(2-hydroxy-ethyl)-1,3-dihydro-indol-2-one (1.6 g, 9.2 mmol), 4-methoxy-3-thiophen-2-yl-benzaldehyde (2 g, 9.2 mmol) and piperidine (4.5 mL, 85 mmol) in ethanol (46 mL) was heated to reflux for overnight. The reaction mixture was concentrated and the residue was chromatographed on a column of silica gel to give 1.63 g (47%) of 4-(2-hydroxy-ethyl)-3-(4-methoxy-3-thiophen-2-yl-benzylidene)-1,3-dihydro-indol-2-one as a yellow orange solid. 1HNMR (300 MHz, DMSO-d6) δ 10.53 (s, br, 1H, NH), 8.73 (d, J=2.1 Hz, 1H), 8.10 (dd, J=2.2 & 9.1 Hz, 1H), 7.74 (s, 1H, H-vinyl), 7.56-7.65 (m, 2H), 7.07-7.22 (m, 3H), 6.81 (d, J=7.5 Hz, 1H), 6.68 (dd, J=0.6, 7.5 Hz, 1H), 4.87 (t, J=4.5 Hz, 1H, OH), 3.97 (s, 3H, OCH3), 3.68-3.75 (m, 2H, CH2CH2OH), 3.09 (t, J=4.5 Hz, 2H, CH2CH2OH).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06689806B1
출처 데이터셋uspto-grants-2004_02
ORD IDord-026f27878bb8434eb2bd152067b6cb4c
출처 메모uspto-grants-2004_02