化工社化工社 化学情報印刷レポート · 研究参考用
1,4-Dioxane → ethyl rac-2-[(1R,2R,4S)-bicyclo[2.2.1]hept-2-ylamino]-4-isopropylpyrimidine-5-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,4-Dioxane | HCID 31275 | — |
| 反応物 | Exo-2-bornanamine | HCID 98480 | — |
| 反応物 | Ethyl 4-isopropyl-2-(methylsulfonyl)pyrimidine-5-carboxylate | HCID 58168829 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | ethyl rac-2-[(1R,2R,4S)-bicyclo[2.2.1]hept-2-ylamino]-4-isopropylpyrimidine-5-carboxylate | HCID 66720026 | 84.4% |
反応手順
To a mixture of ethyl 4-isopropyl-2-(methylsulfonyl)pyrimidine-5-carboxylate (500 mg) and 1,4-dioxane (10 mL) was added exo-2-aminonorbornane (612 mg) at room temperature, and the mixture was stirred at the same temperature for 2 hours. To the reaction mixture was added water, and the aqueous layer was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate) to obtain ethyl rac-2-[(1R,2R,4S)-bicyclo[2.2.1]hept-2-ylamino]-4-isopropylpyrimidine-5-carboxylate (470 mg) as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08524727B2 |
| 出典データセット | uspto-grants-2013_09 |
| ORD ID | ord-b5b7b63357704bcca1194abd21b4cdbd |
| 出典メモ | uspto-grants-2013_09 |