化工社化工社 化学情報印刷レポート · 研究参考用
HRID 75116作成日:2026年10月25日
o-Methylvalerolactim → 3-(3,4-Difluorophenyl)-5,6,7,8-tetrahydroimidazo-[1,5-a]pyridine-1-carboxylic acid
https://huagongshe.com/reaction/75116
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | o-Methylvalerolactim | HCID 138567 | — |
| 反応物 | Lithium hydroxide, monohydrate | HCID 168937 | — |
| 反応物 | 2-(3,4-difluorophenyl)oxazol-5(4H)-one | HCID 58054172 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3-(3,4-Difluorophenyl)-5,6,7,8-tetrahydroimidazo-[1,5-a]pyridine-1-carboxylic acid | HCID 58054185 | 71% |
反応手順
6-methoxy-2,3,4,5-tetrahydropyridine (0.431 g, 3.80 mmol) was dissolved in THF (5 mL) in a 40 mL screw-cap vial and 2-(3,4-difluorophenyl)oxazol-5(4H)-one (0.75 g, 3.80 mmol) in THF (5 mL) was added, producing an orange solution. The vial was capped and heated to 90° C. for 3 hours. THF was removed under reduced pressure and the residue was dissolved in MeOH (10 ml) and lithium hydroxide monohydrate (0.479 g, 11.41 mmol) in water (1 mL) was added. The reaction was heated to 90° C. for 3 hours. MeOH was removed by evaporation under reduced pressure. The remaining aqueous solution was diluted with water (5 mL) and acidified to pH 2 with 5M HCl. The solution was extracted with EtOAc (3×5 mL). The combined organic extracts were dried over anhydrous sodium sulfate, filtered and evaporated to yield the desired product as a brown oil (742 mg, 71%) that was used without further purification. LCMS (+ESI) m/z: 279.3 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US08835422B2 |
|---|
| 出典データセット | uspto-grants-2014_09 |
|---|
| ORD ID | ord-6dfdf4e4b2b14b39b3030a94bfc4e3bf |
|---|
| 出典メモ | uspto-grants-2014_09 |
|---|