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HRID 2212196作成日:2026年10月23日

Triethylamine → 9-Chloro-3-methyl-5-{1-[2-(pyridin-3-yloxy)-acetyl]-piperidin-3-yl}-5H-isoxazolo[4,3-c]quinolin-4-one

https://huagongshe.com/ja/reaction/2212196

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物HOAtHCID 181649—
反応物3-(Pyridin-2-yl)propanoic acidHCID 564292—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物9-Chloro-3-methyl-5-piperidin-3-yl-5H-isoxazolo[4,3-c]quinolin-4-one hydroiodideHCID 21963712—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DimethylformamideHCID 6228—
生成物9-Chloro-3-methyl-5-{1-[2-(pyridin-3-yloxy)-acetyl]-piperidin-3-yl}-5H-isoxazolo[4,3-c]quinolin-4-oneHCID 2196369977.3%

反応手順

Add 9-chloro-3-methyl-5-piperidin-3-yl-5H-isoxazolo[4,3-c]quinolin-4-one hydroiodide (50 mg, 0.11 mmol), 2-pyridine propionic acid (100 mg, 0.33 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (26 mg, 0.13 mmol), 1-hydroxy-7-azabenzotriazole (18 mg, 0.13 mmol), 4-dimethylamino-pyridine (1 mg, 0.01 mmol), and dimethylformamide (3 mL) to a dry roundbottom flask. Stir the reaction under nitrogen, and add triethylamine (30 μL, 0.22 mmol) dropwise. Stir the solution under nitrogen at room temperature overnight. Concentrate the solution and dissolve in 20% isopropanol/chloroform, washed with saturated aqueous sodium bicarbonate solution, brine, dry over magnesium sulfate and concentrate. Purify by flash chromatography on silica gel (eluting with 0–2% methanol/chloroform) to give 38.5 mg of the title compound as a white solid, 76% yield. 1H NMR: consistent with structure. MS (ion spray) 451 (M+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07101891B2
出典データセットuspto-grants-2006_09
ORD IDord-2acb0064197f4046a27b9fbddc1d0c5a
出典メモuspto-grants-2006_09