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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1281392생성일: 2026년 10월 25일

2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline → {5'-[8-(Benzoxazol-2-ylsulfanyl)-octylcarbamoyl]-3,3''-dichloro-[1,1':3'1'']-terphenyl-2'-yloxy}-ethanol

https://huagongshe.com/reaction/1281392

반응식

참여 물질

역할이름HCID투입량
반응물2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinolineHCID 27833—
반응물3,5-Bis(3-chlorophenyl)-4-(2-hydroxyethoxy)benzoic acidHCID 22237395—
반응물8-(Benzoxazol-2-ylsulfanyl)octylamineHCID 22237518—
용매Ethyl AcetateHCID 8857—
용매Npc112006HCID 21965192—
생성물{5'-[8-(Benzoxazol-2-ylsulfanyl)-octylcarbamoyl]-3,3''-dichloro-[1,1':3'1'']-terphenyl-2'-yloxy}-ethanolHCID 8658365874.1%

반응 단계

To a flame dried round bottom flask with 8-(benzoxazol-2-ylsulfanyl)octylamine (0.155 g, 0.558 mmol) in benzene:EtOH (1:1, 6 mL) at room temperature was added 3,5-bis-(m-chlorophenyl)-4-(2-hydroxyethoxy)benzoic acid (0.150 g, 0.372 mmol) followed by EEDQ (0.258 g, 1.04 mmol). After 3 days at this temperature, it was diluted with EtOAc (200 mL). This solution was washed with 1 N HCl (20 mL), sat. aq. NaHCO3 (20 mL), and brine (20 mL) and then dried (MgSO4). After concentration, the residue was purified by preparatory plate chromatography (30% EtOAc/petroleum ether) to afford the product (0.183 g, 74%) as a solid; 1H NMR (CDCl3) δ 1.28-1.42 (m, 6H), 1.42-1.68 (m, 5H), 1.77-1.97 (m, 2H), 3.27-3.41 (m, 6H), 3.46 (dd, J=6.1, 13.5 Hz, 2H), 6.09-6.17 (m, 1H), 7.22-7.47 (m, 7H), 7.47-7.54 (m, 2H), 7.54-7.66 (m, 3H), 7.74 (s, 2H); mass spectrum [(+) ESI], m/z 664 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06451827B2
출처 데이터셋uspto-grants-2002_09
ORD IDord-1cce95a1e00e4ec9b864bac2bbc9082b
출처 메모uspto-grants-2002_09