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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 589097생성일: 2026년 10월 26일

Diisopropylethylamine → N-Methoxy-2-pyridin-2-yl-3,4-dihydroquinoline-1(2H)-carboxamide

https://huagongshe.com/reaction/589097

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Sodium BicarbonateHCID 516892—
반응물4-Nitrophenyl methoxycarbamateHCID 11564735—
반응물2-Pyridin-2-yl-1,2,3,4-tetrahydroquinolineHCID 90409822—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물N-Methoxy-2-pyridin-2-yl-3,4-dihydroquinoline-1(2H)-carboxamideHCID 9040892795%

반응 단계

A solution of 2-pyridin-2-yl-1,2,3,4-tetrahydroquinoline (0.723 g, 3.44 mmol) in methylene chloride (10.3 mL) was treated with 4-nitrophenyl methoxycarbamate (0.948 g, 4.47 mmol) (Org. Process Res. Dev. 2012, 16, 109-116) followed by the dropwise addition of N,N-diisopropylethylamine (1.20 mL, 6.88 mmol), and the resulting mixture was stirred at room temperature for 1.5 h. The reaction mixture was then poured over water (25 mL) and saturated sodium bicarbonate (25 mL) and extracted with dichloromethane (2×50 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated to give a crude oily solid. Purification by flash column chromatography (100% hexanes to 20% ethyl acetate/hexanes [the ethyl acetate contained 5% methanol]) gave the desired product (0.923 g, 95%) as a racemic mixture. LCMS calculated for C16H18N3O2 (M+H)+: m/z=284.1. found: 284.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09227985B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-ab994f55efbd452aa72be3d56fa76a88
출처 메모uspto-grants-2016_01