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HRID 1821916作成日:2026年10月27日

[7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridin-2-yl]methanol → 7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridine-2-carboxaldehyde

https://huagongshe.com/reaction/1821916

反応式

関与物質

役割名称HCID仕込み量
反応物[7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridin-2-yl]methanolHCID 68981956—
触媒HCID 178418406HCID 178418406—
溶媒Methyl, chloro-HCID 5378701—
生成物7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridine-2-carboxaldehydeHCID 5789350360%

反応手順

[7-(Dibenzylamino)-1H-pyrrolo[2,3-c]pyridin-2-yl]methanol (3.0 g, 8.74 mmol) was dissolved in methylene chlorine (175 mL). Manganese dioxide (8.0 g, 92 mmol) was added and the reaction mixture was stirred at room temperature for 20 h. The slurry was filtered through diatomaceous earth to remove the catalyst, and the filtrate was concentrated to a dark oil. Purification by Biotage chromatography (10-30% ethyl acetate in hexanes) provided 7-(dibenzylamino)-1H-pyrrolo[2,3-c]pyridine-2-carboxaldehyde (1.78 g, 60%) as a yellow oil: 1H NMR (300 MHz, CDCl3) δ4.89 (4H, s), 7.06-7.12 (2H, m), 7.27-7.38 (10H, m), 7.93 (1H, d, J=5.7 Hz), 8.74 (1H, br s), 9.77 (1H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07608627B2
出典データセットuspto-grants-2009_10
ORD IDord-c1c4f3fb22ea4648afcab6b4086067e5
出典メモuspto-grants-2009_10