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HRID 1923734作成日:2026年10月27日

4-Fluorobenzoyl chloride → N-(5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)-4-fluorobenzamide

https://huagongshe.com/reaction/1923734

反応式

関与物質

役割名称HCID仕込み量
反応物4-Fluorobenzoyl chlorideHCID 67879—
反応物5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-amineHCID 60205276—
溶媒PyridineHCID 1049—
生成物N-(5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)-4-fluorobenzamideHCID 6020534978.3%

反応手順

4-Fluorobenzoyl chloride (0.15 mL, 1.30 mmol) was added to 5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-amine (200 mg, 0.87 mmol, Example 1, Step H) in pyridine (5 mL). The reaction was stirred at room temperature for 10 minutes, and then the pyridine was removed. THF (5 mL) and 2N LiOH (3 mL) were added and stirred for 20 minutes. The THF was removed, and water (20 mL) was added. The solid formed was collected by filtration and dried to give N-(5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)-4-fluorobenzamide (0.24 g, 77% yield) as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08178131B2
出典データセットuspto-grants-2012_05
ORD IDord-3636d7889ecb43d2aa3ff66a07486380
出典メモuspto-grants-2012_05