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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

反応式

関与物質

役割名称HCID仕込み量
反応物HydrazineHCID 9321—
反応物Phenylimidocarbonyl chlorideHCID 12145—
反応物DiisopropylethylamineHCID 81531—
反応物5-Isopropyl-2,4-dimethoxy-n-(1-methyl-1h-indol-5-yl)-thiobenzamideHCID 59729557—
溶媒1,4-DioxaneHCID 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]-phenylamineHCID 59729571—

反応条件

温度100 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08053456B2
出典データセットuspto-grants-2011_11
ORD IDord-a105fc2b3ee5488883dcfe83a1d5040a
出典メモuspto-grants-2011_11