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HRID 537849作成日:2026年10月24日
N-(3-Aminophenyl)-1-phenylmethanesulfonamide → N-(3-((5-(4-cyanophenyl)oxazol-2-yl)amino)phenyl)-1-phenylmethanesulfonamide
https://huagongshe.com/ja/reaction/537849
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | N-(3-Aminophenyl)-1-phenylmethanesulfonamide | HCID 16772451 | — |
| 反応物 | 4-(2-Chlorooxazol-5-yl)benzonitrile | HCID 68443558 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | N-(3-((5-(4-cyanophenyl)oxazol-2-yl)amino)phenyl)-1-phenylmethanesulfonamide | HCID 71060644 | — |
反応手順
A mixture of 4-(2-chlorooxazol-5-yl)benzonitrile 2 (0.20 g, 0.98 mmol) and N-(3-aminophenyl)-1-phenylmethanesulfonamide 4 (0.256 g, 0.98 mmol) in 2-propanol (20 mL) was heated to 80° C. for 18 h with stirring. Upon cooling, a white solid precipitated out which was filtered off, washed with 2-propanol, and dried. This was then triturated with ether and filtered to yield the title product, a white solid, as the hydrochloride salt of 5 (0.15 g, 36%). Free amine containing filtrate was evaporated and silica column purified (Biotage) (Acetone/hexane as an eluent) to provide 5 (0.15 g, 36% yield) as pale yellow solid. MS (ES) m/z 431 (M+H+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08865709B2 |
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| 出典データセット | uspto-grants-2014_10 |
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| ORD ID | ord-2c17b9bee21e4cc08df6e108e92c2e04 |
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| 出典メモ | uspto-grants-2014_10 |
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