化工社化工社 化学情報印刷レポート · 研究参考用
Sodium borohydride → 6-{4-[(2-Cyclopentyl-ethylamino)-methyl]-phenoxy}-nicotinamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | 2-Cyclopentylethanamine | HCID 5305650 | — |
| 反応物 | 6-(4-Formylphenoxy)pyridine-3-carboxamide | HCID 56851422 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 6-{4-[(2-Cyclopentyl-ethylamino)-methyl]-phenoxy}-nicotinamide | HCID 59730261 | 52.2% |
反応手順
Combine 6-(4-formyl-phenoxy)-nicotinamide (0.61 g, 2.54 mmol) with 2-Cyclopentyl-ethylamine (0.38 g, 3.3 mmol), 2 g of 3 {acute over (Å)} molecular sieves, and 10 mL of methanol. Stir for 18 h under nitrogen. Add sodium borohydride (0.5 g, 13.2 mmol), and stir for 24 h. Filter through Celite, remove the solvent in vacuo. Partition the residue between water (50 mL) and ethyl acetate (100 mL). Dry the organic phase (sodium sulfate), filter, and concentrate in vacuo. Adsorb on silica, and purify on an ISCO® 100 g system (eluting with 95:5:0.5 to 90:10:1 chloroform/ethanol/ammonium hydroxide) to afford 0.45 g of product. HPLC retention time: 5.93 min (98.7% purity), ESMS (M+): 340.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07381719B2 |
| 出典データセット | uspto-grants-2008_06 |
| ORD ID | ord-84f3d6a721274a9d824451f4301ec669 |
| 出典メモ | uspto-grants-2008_06 |