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HRID 2399448作成日:2026年10月25日

3-(4-benzyloxyphenyl)methyl-7-methyl-2-propyl-3H-imidazo[4,5-b]pyridine → 3-(4-hydroxyphenyl)methyl-7-methyl-2-propyl-3H-imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/2399448

反応式

関与物質

役割名称HCID仕込み量
反応物3-(4-benzyloxyphenyl)methyl-7-methyl-2-propyl-3H-imidazo[4,5-b]pyridineHCID 19385692—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物3-(4-hydroxyphenyl)methyl-7-methyl-2-propyl-3H-imidazo[4,5-b]pyridineHCID 1938564382%

反応手順

To a solution of the product of Step C (0.60 g, 1.62 mmol) in 10 mL of MeOH was added 60 mg of a 10% Pd/C catalyst and was stirred under a H2 atmosphere (1 atm) for 7 hours. The reaction mixture was then filtered through magnesium sulfate and the filtrate was concentrated in vacuo to yield 0.372 g (82%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05449682
出典データセットuspto-grants-1995_09
ORD IDord-d20be1c7f9f54e5e9a77dc5804d42c3d
出典メモuspto-grants-1995_09