関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | N-Benzyl-6-chloro-nicotinamide | HCID 857488 | — |
| 反応物 | HCID 178424304 | HCID 178424304 | — |
| 触媒 | Manganese triacetate dihydrate | HCID 12416832 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | N-benzyl-6-chloro-4-o-tolyl-nicotinamide | HCID 12167314 | 89.1% |
反応手順
A solution of 0.5 g (2.0 mMol) N-benzyl-6-chloro-nicotinamide in 5.0 ml THF was added over 25 minutes to 10.1 ml (10.1 mMol) of o-tolylmagnesium chloride solution (1M in THF) cooled to 0° C. After 2.5 hours stirring at room temperature, the reaction mixture was cooled again to 0° C. and 4.0 ml acetic acid were added over 15 minutes followed by 1.1 g (4.1 mMol) manganese triacetate dihydrate. After stirring for 1 hour at room temperature, the reaction mixture was filtered and the filtrate was poured onto 20 ml deionized water. Sodium bicarbonate was added portionwise to bring the pH to 7 and the phases were separated. The aqueous layer was extracted with dichloromethane. The combined organic extracts were washed with water, dried (Na2SO4) and evaporated. The residue was purified by flash chromatography (eluent ethyl acetate/n-hexane 2:1) to yield 0.6 g (88%) N-benzyl-6-chloro-4-o-tolyl-nicotinamide as an orange resin.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06297375B1 |
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| 出典データセット | uspto-grants-2001_10 |
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| ORD ID | ord-9c1004844e1743f5ab97ad94b3f4675d |
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| 出典メモ | uspto-grants-2001_10 |
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