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HRID 16403作成日:2026年10月24日

Hydrochloric Acid → 4-Chloro-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/ja/reaction/16403

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Isoamyl NitriteHCID 8053—
反応物1H-pyrrolo(2,3-b)pyridin-4-amineHCID 639249—
触媒Cuprous chlorideHCID 62652—
溶媒Acetic AcidHCID 176—
溶媒Sulfuric AcidHCID 1118—
生成物4-Chloro-1H-pyrrolo[2,3-b]pyridineHCID 11389493—

反応条件

温度12 °C

反応手順

750 mg (5.63 mmol) of 4-amino-1H-pyrrolo[2,3-b]pyridine (from example XVII) are dissolved in a mixture of 67.5 ml of glacial acetic acid and 0.67 ml of concentrated sulfuric acid. The mixture is cooled to 12° C. 3.67 ml (3.20 g, 117 mmol) of isopentyl nitrite are slowly added dropwise, and the mixture is stirred at 12° C. for 3 hours. This solution is then added to a suspension (temperature: 50° C.) of 6.07 g (61.4 mmol) of copper(I) chloride in 34 ml of concentrated hydrochloric acid, and the mixture is then heated at 80-90° C. for 30 min. The mixture is cooled to RT and stirred overnight. For work-up, the reaction solution is concentrated and made alkaline using 1N aqueous sodium hydroxide solution, the precipitated copper salts are filtered off with suction through kieselguhr and the mixture is extracted 3× with ethyl acetate. The organic phase is dried over magnesium sulfate and concentrated using a rotary evaporator.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737153B2
出典データセットuspto-grants-2010_06
ORD IDord-9f489cee178a4a85820a21148e07dc4d
出典メモuspto-grants-2010_06