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HRID 1641458作成日:2026年10月27日
Hydrochloric Acid → 3-bromo-N-(4-chloro-2-(1-cyclopropylethylcarbamoyl)phenyl)-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxamide
https://huagongshe.com/reaction/1641458
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 反応物 | 2-amino-5-chloro-N-(1-cyclopropylethyl)benzamide | HCID 43533096 | — |
| 反応物 | phenyl 3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylate | HCID 66737070 | — |
| 溶媒 | Dimethyl Sulfoxide | HCID 679 | — |
| 生成物 | 3-bromo-N-(4-chloro-2-(1-cyclopropylethylcarbamoyl)phenyl)-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxamide | HCID 66736193 | 38.6% |
反応手順
0.18 g of potassium tert-butoxide was added to a mixed solution comprising 0.23 g of 2-amino-5-chloro-N-(1-cyclopropylethyl)benzamide, 0.30 g of phenyl 3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylate and 5 ml of dimethyl sulfoxide, followed by reaction at room temperature for 1 hour. The reaction liquid was slowly added to diluted hydrochloric acid, the mixed liquid was subjected to extraction with ethyl acetate, and the organic layer was washed with a saturated sodium hydrogen carbonate aqueous solution and with a sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=8/2 to 7.5/2.5) to obtain 0.16 g of the desired product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08115006B2 |
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| 出典データセット | uspto-grants-2012_02 |
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| ORD ID | ord-5c7e743ed5b64bc7bde86b38793f0962 |
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| 出典メモ | uspto-grants-2012_02 |
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