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HRID 1440104作成日:2026年10月27日
HCID 178471895、化合物 → ethyl 2-[2-amino-5-(difluoromethoxy)-3,4,6-trifluorobenzoyl]-3-(cyclopropylamino)prop-2-enoate
https://huagongshe.com/reaction/1440104
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | HCID 178471895 | HCID 178471895 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | ethyl 2-[2-amino-5-(difluoromethoxy)-3,4,6-trifluorobenzoyl]-3-(cyclopropylamino)prop-2-enoate | HCID 178471897 | 80.6% |
反応手順
33.63 g (0.079 mole) of ethyl 3-cyclopropylamino-2-(3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl)acrylate [(XIXa): X=X'=F, R1 =OCHF2, R17 =C2H5 ] were dissolved in 1300 ml of ethanol with heating. A stream of hydrogen was then bubbled through the solution in the presence of 8.4 g of 5% palladium-on-carbon at room temperature for 40 minutes, whilst stirring. At the end of this time, the reaction mixture was filtered, and the filtrate was concentrated by evaporation under reduced pressure. The resulting residue was then purified by silica gel column chromatography using a 9:1 by volume mixture of toluene and ethyl acetate as the eluent, to give 25.1 g of ethyl 3-cyclopropylamino-2-(6-amino-3-difluoromethoxy-2,4,5-trifluorobenzoyl)acrylate [(XIXb): X=X'=F, R1 =OCHF2, R17 =C2H5 ] as a pale yellow powder, melting at 103°-104° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05496951 |
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| 出典データセット | uspto-grants-1996_03 |
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| ORD ID | ord-3b3e78adf13e4ba18bb410a0a0e75276 |
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| 出典メモ | uspto-grants-1996_03 |
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