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HRID 1820904作成日:2026年10月27日

Iodine → 5-(3,4-Dimethoxy-phenyl)-3-iodo-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/1820904

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Sodium Thiosulfate PentahydrateHCID 61475—
反応物5-(3,4-Dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridineHCID 10149230—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物5-(3,4-Dimethoxy-phenyl)-3-iodo-1H-pyrrolo[2,3-b]pyridineHCID 59812169—

反応条件

温度-40 °C

反応手順

5-(3,4-Dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridine, 82, (0.270 g, 0.00106 mol) was dissolved in Tetrahydrofuran (8.5 mL, 0.10 mol) under an atmosphere of Nitrogen. The solution was stirred at −40° C. and Iodine (0.269 g, 0.00106 mol) dissolved in 2.5 mL of Tetrahydrofuran was added. The chilled reaction mixture was stirred for 2 h and was then quenched with the addition of Sodium thiosulfate, pentahydrate (0.13 g, 0.00053 mol) in water (1M). The reaction mixture was partitioned between water (20 mL and ethyl acetate (30 mL). The two layers were seperated, and the aquous layer was extracted with ethyl acetate. The organic layers were washed with water and brine, dried with sodium sulfate, then concentrated under reduced pressure. The dark colored crude residue was carried onto the next reaction without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07605168B2
出典データセットuspto-grants-2009_10
ORD IDord-7b79f6b007bb4427876698b4723b5ba2
出典メモuspto-grants-2009_10