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HRID 84375作成日:2026年10月24日

6-Bromo-3-pyridinecarboxaldehyde → 6-(7-(2-Fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)nicotinaldehyde

https://huagongshe.com/ja/reaction/84375

反応式

関与物質

役割名称HCID仕込み量
反応物6-Bromo-3-pyridinecarboxaldehydeHCID 11769234—
反応物7-(2-Fluoro-4-nitrophenoxy)-2-iodothieno[3,2-b]pyridineHCID 59457661—
反応物HCID 178477788HCID 178477788—
溶媒1,4-DioxaneHCID 31275—
生成物6-(7-(2-Fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)nicotinaldehydeHCID 5945766650.2%

反応条件

温度100 °C

反応手順

To a solution of 7-(2-fluoro-4-nitrophenoxy)-2-iodothieno[3,2-b]pyridine (24) [US 2006/0287343 A1] (6 g, 14.42 mmol) in dioxane (40 mL) were added 6-bromopyridine-3-carbaldehyde (3.22 g, 17.30 mmol), palladium tetrakistriphenylphosphine (0.500 g, 0.433 mmol) and hexamethyldistannane (3.29 mL, 15.86 mmol). The mixture was heated at 100° C. for 20 h. It was then concentrated and adsorbed on silica gel, transferred onto a silica gel column and eluted with DCM/MeOH (100/0, 99/1, 98/2, 97/3) to afford title compound 123 (2.864 g, 50% yield). MS (m/z): 396.1 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846927B2
出典データセットuspto-grants-2014_09
ORD IDord-af4c3697ce7a4cc692ebf431b4df3f46
出典メモuspto-grants-2014_09