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Pyrazole → methyl 6-(1H-pyrazol-1-yl)nicotinate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyrazole | HCID 1048 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Methyl 6-chloropyridine-3-carboxylate | HCID 254249 | — |
| 溶媒 | Dimethyl Sulfoxide | HCID 679 | — |
| 生成物 | methyl 6-(1H-pyrazol-1-yl)nicotinate | HCID 3741563 | 93% |
反応手順
To a solution of pyrazole (19.4 g, 0.28 mol) in 100 mL anhydrous DMSO, which was at a temperature of 0° C., was added NaH (7.5 g, 0.3 mol) gradually over a period of 30 min. The resulting reaction mixture was allowed to warm to room temperature, at which the mixture continued to agitate for an additional 30 min. Methyl 6-chloronicotinate (35 g, 0.2 mol) was added to the stirring reaction mixture and agitated vigorously for a period of 6 hr. The reaction mixture was subsequently cooled to a temperature of about 0° C. and poured into a saturated aqueous, 0° C. NH4Cl solution. The resulting precipitate was filtered, washed with water, and dried to give a compound of formula (XI-a) (38.3 g, 93% yield) as an off-white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07135573B2 |
| 出典データセット | uspto-grants-2006_11 |
| ORD ID | ord-0599d0c7b18f4778a3a100508a329676 |
| 出典メモ | uspto-grants-2006_11 |