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HRID 501956作成日:2026年10月26日

1,4'-Bipiperidine → (R)-3-(7-Methyl-1H-indazol-5-yl)-1-oxo-1-(4-(piperidin-1-yl)piperidin-1-yl)propan-2-yl 4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/501956

反応式

関与物質

役割名称HCID仕込み量
反応物1,4'-BipiperidineHCID 78607—
反応物DiisopropylethylamineHCID 81531—
反応物PyBOPHCID 2724699—
反応物(R)-3-(7-Methyl-1H-indazol-5-yl)-2-(4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carbonyloxy)propanoic acidHCID 59424312—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物(R)-3-(7-Methyl-1H-indazol-5-yl)-1-oxo-1-(4-(piperidin-1-yl)piperidin-1-yl)propan-2-yl 4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxylateHCID 11685954—

反応条件

温度0 °C

反応手順

To a solution of (R)-3-(7-methyl-1H-indazol-5-yl)-2-(4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carbonyloxy)propanoic acid (500 mg, 1.05 mmol), diisopropylethylamine (0.37 mL, 2.11 mmol), and 4-piperidinopiperidine (355 mg, 2.0 equiv) in dimethylformamide (4 mL) and dichloromethane (4 mL) at 0° C. was added PyBOP® (576 mg, 1.11 mmol). The reaction was stirred at 0° C. for 4 h, was concentrated, and purified by column chromatography (95:5:1 to 93:7:1 dichloromethane/methanol/triethylamine). The resulting residue was dissolved in 5% methanol/dichloromethane and passed through a basic alumina column to give 600 mg (88%) as a white powder. Mass spec.: 625.56 (MH)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07772244B2
出典データセットuspto-grants-2010_08
ORD IDord-0055b98dd3d247bbb00da879f4195822
出典メモuspto-grants-2010_08