참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2-(Trifluoromethyl)benzoyl chloride | HCID 67561 | — |
| 반응물 | 2-amino-1-(3,5-dichloropyridin-2-yl)ethanone-O-ethyloxime | HCID 118071516 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-[2-(3,5-dichloropyridin-2-yl)-2-(ethoxyimino)ethyl]-2-(trifluoromethyl)benzamide | HCID 131736883 | 56.1% |
반응 단계
To a solution of 200 mg of 2-amino-1-(3,5-dichloropyridin-2-yl)ethanone-β-ethyloxime and 90 mg of triethylamine in 3 ml of dichloromethane, 169 mg of 2-(trifluoromethyl)benzoyl chloride was added dropwise with stirring under cooling with ice, and after the addition, the mixture was stirred at room temperature for another 30 minutes. After completion of the reaction, the reaction mixture was mixed with 10 ml of water and extracted with ethyl acetate (15 ml×1), the resulting organic layer was washed with water (10 ml×1) and dried over saturated aqueous sodium chloride and then anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography using ethyl acetate-hexane (with a gradient of from 1:9 to 3:7) as the eluent to obtain 190 mg of the desired product as a pale yellow resinous substance.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09434684B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-9054a357c6634b4abced56e566dacb4b |
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| 출처 메모 | uspto-grants-2016_09 |
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