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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,4'-Bipiperidine | HCID 78607 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | PyBOP | HCID 2724699 | — |
| 反応物 | (+/-)-2-Hydroxy-3-(7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)propanoic acid | HCID 59424315 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Ethyl Acetate | HCID 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-one | HCID 59424337 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07772244B2 |
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| 出典データセット | uspto-grants-2010_08 |
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| ORD ID | ord-4091db7fdc48467ba9dfa7c6a916c613 |
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| 出典メモ | uspto-grants-2010_08 |
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