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HRID 501967作成日:2026年10月25日

1,4'-Bipiperidine → (+/-)-2-hydroxy-3-(7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)-1-(4-(piperidin-1-yl)piperidin-1-yl)propan-1-one

https://huagongshe.com/reaction/501967

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(+/-)-2-Hydroxy-3-(7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)propanoic acidHCID 59424315—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物(+/-)-2-hydroxy-3-(7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)-1-(4-(piperidin-1-yl)piperidin-1-yl)propan-1-oneHCID 59424337—

反応条件

温度0 °C

反応手順

To a solution of (±)-2-hydroxy-3-(7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)propanoic acid (100 mg, 0.29 mmol), 4-piperidinopiperidine (96.0 mg, 2.0 equiv), and diisopropylethylamine (0.10 mL, 0.57 mmol) in dichloromethane (3.6 mL) at 0° C. was added PyBOP® (156 mg, 0.30 mmol) in two portions. The reaction was stirred at 0° C. for 15 minutes and at room temperature overnight. The reaction was diluted with ethyl acetate, washed with water (2×), then brine, dried over magnesium sulfate, and concentrated. Column chromatography (4% to 10% methanol/dichloromethane) gave 130 mg (91%) as an oil. Mass spec.: 501.36 (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-4091db7fdc48467ba9dfa7c6a916c613
出典メモuspto-grants-2010_08