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HRID 589097作成日:2026年10月26日

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

https://huagongshe.com/reaction/589097

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Sodium BicarbonateHCID 516892—
反応物4-Nitrophenyl methoxycarbamateHCID 11564735—
反応物2-Pyridin-2-yl-1,2,3,4-tetrahydroquinolineHCID 90409822—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物N-Methoxy-2-pyridin-2-yl-3,4-dihydroquinoline-1(2H)-carboxamideHCID 9040892795%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09227985B2
出典データセットuspto-grants-2016_01
ORD IDord-ab994f55efbd452aa72be3d56fa76a88
出典メモuspto-grants-2016_01