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HRID 522227作成日:2026年10月24日

Iodine → 4-Bromo-2-iodo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/ja/reaction/522227

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Lithium diisopropylamideHCID 2724682—
反応物4-Bromo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-B]pyridineHCID 45074561—
溶媒TetrahydrofuranHCID 8028—
生成物4-Bromo-2-iodo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridineHCID 46907955—

反応条件

温度-78 °C

反応手順

To a −78° C. solution of Example 135A (250 mg, 0.741 mmol) in 10 mL tetrahydrofuran was added lithium diisopropylamide (2.0M solution in tetrahydrofuran, 0.556 mL, 1.112 mmol) slowly over the course of 5 minutes. The resulting solution was stirred at the same temperature for 30 minutes after which iodine (376 mg, 1.483 mmol) in 5 mL of tetrahydrofuran was slowly added over 10 minutes. The reaction was stirred at −78° C. for 2.5 hours, and was quenched by addition of 1M aqueous sodium thiosulfate solution. The mixture was extracted with dichloromethane. The combined organic layers were washed with brine, dried over MgSO4, filtered, and concentrated to give the title compound. MS (ESI+) m/z 462 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09328112B2
出典データセットuspto-grants-2016_05
ORD IDord-18091cced3024011912f07ec0df5ca20
出典メモuspto-grants-2016_05