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HRID 350294作成日:2026年10月27日
Water → ethyl [1-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-3-pyridylmethyl]-3-phenyl-1H-pyrazol-4-yl]acetate
https://huagongshe.com/reaction/350294
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 5-Chloromethyl-2-(5-methyl-2-phenyl-4-oxazolyl)methoxypyridine | HCID 17832808 | — |
| 反応物 | HCID 178470745 | HCID 178470745 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | ethyl [1-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-3-pyridylmethyl]-3-phenyl-1H-pyrazol-4-yl]acetate | HCID 86760432 | 58% |
反応手順
Sodium hydride (60%, oily, 70.0 mg) was added to a solution of 5-chloromethyl-2-(5-methyl-2-phenyl-4-oxazolylmethoxy)pyridine (551 mg) and ethyl(3-phenyl-1H-pyrazol-4-yl)acetate (403 mg) in N,N-dimethylformamide (10 ml) at 0° C., and the mixture was stirred at room temperature for 1 hour. The reaction mixture was poured into water, and extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4), and concentrated. The residue was subjected to silica gel column chromatography to obtain ethyl [1-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-3-pyridylmethyl]-3-phenyl-1H-pyrazol-4-yl]acetate (513 mg, yield: 58%) as a colorless oily substance from the fraction eluted with ethyl acetate-hexane (2:3, volume ratio).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07179823B1 |
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| 出典データセット | uspto-grants-2007_02 |
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| ORD ID | ord-6389470430234a8bac43a1a3769be4a7 |
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| 出典メモ | uspto-grants-2007_02 |
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