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HRID 76104作成日:2026年10月24日
Ammonium Chloride → 4-Isopropyl-6-[4-(1-methyl-1H-indol-5-yl)-5-phenylamino-4H-[1,2,4]triazol-3-yl]-benzene-1,3-diol
https://huagongshe.com/ja/reaction/76104
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Einecs 211-027-4 | HCID 69401 | — |
| 反応物 | [5-(5-isopropyl-2,4-dimethoxy-phenyl)-4-(1-methyl-1H-indol-5-yl)-4H-[1,2,4]triazol-3-yl]-phenylamine | HCID 59729571 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-Isopropyl-6-[4-(1-methyl-1H-indol-5-yl)-5-phenylamino-4H-[1,2,4]triazol-3-yl]-benzene-1,3-diol | HCID 135971866 | 66.7% |
反応手順
A flask was charged with [5-(5-Isopropyl-2,4-dimethoxy-phenyl)-4-(1-methyl-1H-indol-5-yl)-4H-[1,2,4]triazol-3-yl]-phenyl-amine (27 mg; 0.06 mmol) and pyridinium chloride (2 g.). The reactants were placed under a nitrogen atmosphere, and the reaction was heated to 210° C. for 25 minutes. To the cooled reaction mixture was added dichloromethane and saturated ammonium chloride solution. The organic fraction was isolated, and the product was purified by column chromatography to give 4-Isopropyl-6-[4-(1-methyl-1H-indol-5-yl)-5-phenylamino-4H-[1,2,4]triazol-3-yl]-benzene-1,3-diol (18 mg; 0.04 mmol.)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08835464B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-ca50e995b3fa4a0a90d8e327a12543be |
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| 出典メモ | uspto-grants-2014_09 |
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