関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Ethyl-2-methylpyridine | HCID 68307 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 反応物 | HCID 178520036 | HCID 178520036 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | HCID 178436305 | HCID 178436305 | 32% |
反応手順
To a stirred solution of 4-ethyl-2-methylpyridine (0.458 9, 3.79 mmol) in THF (4mL) at −50 degrees Celsius, add butyl lithium (1.5 mL, 2.5 M, 3.79 mmol) slowly and stir for 10 minutes. To the reaction, slowly add a solution of 6-Chloro-1H-indazole-3-carbaldehyde (0.5 g, 1.89 mmol) in THF (4 mL). After stirring for 10 minutes, the reaction was quenched with 1 N citric acid (10 mL). The mixture was diluted with EtOAc (50 mL), water (20 mL), and saturated NaCl (10 mL). The layers were separated, and the aqueous was extracted with EtOAc (3×15 mL). The organics were combined and washed with saturated NaCl (20 mL). After drying the organic layer over Na2SO4, the solids were removed by filtration and the liquid was concentrated to an oil by rotary evaporation. Chromatography (40 g silica gel, 60–100% EtOAc/hex) yields the desired product (142 mg, 32%) and recovered 6-Chloro-1H-indazole-3-carbaldehyde (348 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07053107B2 |
|---|
| 出典データセット | uspto-grants-2006_05 |
|---|
| ORD ID | ord-1cf3762e7edb43eba9e8b60d8675ebcc |
|---|
| 出典メモ | uspto-grants-2006_05 |
|---|