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HRID 555946作成日:2026年10月26日
Hydrazine → [5-(5-isopropyl-2,4-dimethoxy-phenyl)-4-(1-methyl-1H-indol-5-yl)-4H-[1,2,4]triazol-3-yl]-phenylamine
https://huagongshe.com/reaction/555946
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Hydrazine | HCID 9321 | — |
| 反応物 | Phenylimidocarbonyl chloride | HCID 12145 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 5-Isopropyl-2,4-dimethoxy-n-(1-methyl-1h-indol-5-yl)-thiobenzamide | HCID 59729557 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | [5-(5-isopropyl-2,4-dimethoxy-phenyl)-4-(1-methyl-1H-indol-5-yl)-4H-[1,2,4]triazol-3-yl]-phenylamine | HCID 59729571 | — |
反応手順
A flask was charged with 5-isopropyl-2,4-dimethoxy-N-(1-methyl-1H-indol-5-yl)-thiobenzamide (123 mg; 0.33 mmol), dioxane (2 mL), and hydrazine (0.5 mL). The reaction was heated to 100° C. for one hour, and the solvent was removed by evaporation. To the solid cake was added ethyl acetate (10 mL) and 10% aqueous potassium carbonate (1 mL), and it was shaken until the solid was completely dissolved. The organic layer was isolated, and dried with sodium sulfate. To the crude intermediate in the organic layer was added diisopropylethylamine (86 mg, 0.66 mmol) and phenylisocyanide dichloride (88 mg; 1.5 eq.). The reaction was stirred overnight, and washed with saturated aqueous ammonium chloride, dried with sodium sulfate, and the product was purified by column chromatography to give [5-(5-Isopropyl-2,4-dimethoxy-phenyl)-4-(1-methyl-1H-indol-5-yl)-4H-[1,2,4]triazol-3-yl]-phenyl-amine (64 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08053456B2 |
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| 出典データセット | uspto-grants-2011_11 |
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| ORD ID | ord-a105fc2b3ee5488883dcfe83a1d5040a |
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| 出典メモ | uspto-grants-2011_11 |
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