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HRID 1519258作成日:2026年10月25日
2'-Nitro-4-thiocarbamoyl-biphenyl-2-carboxylic acid methyl ester → 4-[4-(4-Fluoro-phenyl)-thiazol-2-yl]-2'-nitro-biphenyl-2-carboxylic acid methyl ester
https://huagongshe.com/reaction/1519258
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 2'-Nitro-4-thiocarbamoyl-biphenyl-2-carboxylic acid methyl ester | HCID 86679832 | — |
| 反応物 | 4-[4-(4-Fluoro-phenyl)-thiazol-2-yl]-2'-nitro-biphenyl-2-carboxylic acid methyl ester 4-Fluorophenacyl bromide | HCID 86679838 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 4-[4-(4-Fluoro-phenyl)-thiazol-2-yl]-2'-nitro-biphenyl-2-carboxylic acid methyl ester | HCID 86679837 | 57.5% |
反応手順
4-[4-(4-Fluoro-phenyl)-thiazol-2-yl]-2′-nitro-biphenyl-2-carboxylic acid methyl ester 4-Fluorophenacyl bromide (available from Alfa Aesar; 35 mg, 0.16 mmol) was added to a suspension of 2′-nitro-4-thiocarbamoyl-biphenyl-2-carboxylic acid methyl ester (which may be prepared as described for Intermediate 4; 50 mg, 0.16 mmol) in ethanol (2 mL) and the resulting mixture was stirred at 45° C. for 20 h. The reaction mixture was concentrated to a small volume and cooled. The precipitate was collected by filtration to give 4-[4-(4-fluoro-phenyl)-thiazol-2-yl]-2′-nitro-biphenyl-2-carboxylic acid methyl ester (40 mg) which was used directly in the next step without purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09073881B2 |
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| 出典データセット | uspto-grants-2015_07 |
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| ORD ID | ord-94e822ac3930439782e9bac5ab1fb868 |
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| 出典メモ | uspto-grants-2015_07 |
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