化工社化工社 化学情報印刷レポート · 研究参考用
4-Methylnicotinic acid Hydrochloride → 4-Methylpiperidine-3-carboxylic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Methylnicotinic acid Hydrochloride | HCID 2796506 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 触媒 | Adams' catalyst | HCID 345198 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | 4-Methylpiperidine-3-carboxylic acid | HCID 13658609 | — |
反応手順
AcOH (380 mL) was added to 4-methylnicotinic acid hydrochloride (50.5 g, 291 mmol, Maybridge) and PtO2 (5.05 g, 22.2 mmol, Johnson Matthey) in a 600 mL stainless steel reactor. The mixture was stirred under 220 psi of hydrogen at ambient temperature for about 14 hr. The supernatant solution was filtered through a nylon membrane and rinsed with enough AcOH until only the catalyst remained. The filtrate was concd under reduced pressure to give a clear oil that solidified upon cooling to ambient temperature to give crude 4-methylpiperidine-3-carboxylic acid with AcOH as an excipient (88.94 g, 170%): LC/MS (Table 1, Method b) Rt=0.44 min; MS m/z: 144 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08426411B2 |
| 出典データセット | uspto-grants-2013_04 |
| ORD ID | ord-683763b43ab047b0854bd0249ed5ebf2 |
| 出典メモ | uspto-grants-2013_04 |