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HRID 2187814作成日:2026年10月25日
1-(4-Chlorobenzyl)-4-[[(N-Boc-valyl)amino]methyl]piperidine → 1-(4-Chlorobenzyl)-4-[(valylamino)methyl]piperidine
https://huagongshe.com/reaction/2187814
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 1-(4-Chlorobenzyl)-4-[[(N-Boc-valyl)amino]methyl]piperidine | HCID 18711802 | — |
| 溶媒 | Hydrochloride methanol | HCID 21893726 | — |
| 生成物 | 1-(4-Chlorobenzyl)-4-[(valylamino)methyl]piperidine | HCID 53782731 | 97% |
反応手順
1-(4-Chlorobenzyl)-4-[{(N-Boc-valyl)amino}methyl]piperidine (1.1 g, 2.51 mmol) was dissolved in 3 M HCl-CH3OH solution (25 mL) and stirred at 25° C. for 1 h. The reaction mixture was concentrated and the resulting salt was dissolved in 3:1 tBuOH—H2O (25 mL). Anion (OH−) exchange resin was added until the solution was slightly basic. Filtration and concentration afforded 1(4-chlorobenzyl)-4-{(valylamino)methyl}piperidine (819 mg, 97%) which required no further purification: RPLC (97%); ESI/MS 338.1 (M++H, C19H28ClN3O).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06410566B1 |
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| 出典データセット | uspto-grants-2002_06 |
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| ORD ID | ord-583a93977f5a457c9fbac88310f01a8f |
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| 出典メモ | uspto-grants-2002_06 |
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