関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Ethyl 3-oxohexanoate | HCID 238498 | — |
| 反応物 | Sodium ethoxide | HCID 2723922 | — |
| 反応物 | 4-azido-N-(2-piperidin-1-ylethyl)benzamide | HCID 86629800 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | HCID 68513562 | HCID 68513562 | 92.9% |
反応手順
4-Azido-N-(2-piperidin-1-ylethyl)benzamide obtained in Example 62a) and ethyl 3-oxohexanoate (1.08 ml, 6.44 mmol, 1.25 eq.) were dissolved in ethanol (20 ml), sodium ethoxide (487 mg, 6.44 mmol, 1.25 eq.) was added, and the mixture was stirred at room temperature for 30 min, and then at 60° C. for 13 hr. Water (40 ml) was added to the reaction mixture, ethanol was evaporated, and the residue was washed twice with ethyl acetate-hexane (2:1, 50 ml). The aqueous layer was neutralized (pH 6-7) with 6N hydrochloric acid and concentrated. The residue was dissolved in isobutanol, THF and ethyl acetate, dried over anhydrous sodium sulfate and concentrated, and ethyl acetate and THF were added to the residue. The precipitate was collected by filtration, washed with ethyl acetate and dried to give the title compound as a pale-brown powder (purity 90%, 2.05 g, 4.78 mmol, 92.9%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07803822B2 |
|---|
| 出典データセット | uspto-grants-2010_09 |
|---|
| ORD ID | ord-d38b9edfaa1d451a813432c4d8d294ae |
|---|
| 出典メモ | uspto-grants-2010_09 |
|---|