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HRID 7493作成日:2026年10月26日

4-(5-Benzyloxy-2-fluoro-4-methylphenoxy)-6-methoxy-7-(2-methoxyethoxy)cinnoline → 4-(2-Fluoro-5-hydroxy-4-methylphenoxy)-6-methoxy-7-(2-methoxyethoxy)cinnoline

https://huagongshe.com/reaction/7493

反応式

関与物質

役割名称HCID仕込み量
反応物4-(5-Benzyloxy-2-fluoro-4-methylphenoxy)-6-methoxy-7-(2-methoxyethoxy)cinnolineHCID 21991063—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
溶媒DimethylformamideHCID 6228—
生成物4-(2-Fluoro-5-hydroxy-4-methylphenoxy)-6-methoxy-7-(2-methoxyethoxy)cinnolineHCID 2199106446.5%

反応手順

A solution of 4-(5-benzyloxy-2-fluoro-4-methylphenoxy)-6-methoxy-7-(2-methoxyethoxy)cinnoline (242 mg 0.5 mmol) in a mixture of methanol (9 ml) and DMF (10.5 ml) containing 10% palladium-on-charcoal catalyst (100 mg) was stirred under hydrogen at 5 atmospheres pressure for 9 hours. The catalyst was removed by filtration and the solvent was evaporated. The residue was washed with methanol and ether and dried under vacuum to give 4-(2-fluoro-5-hydroxy-4-methylphenoxy)-6-methoxy-7-(2-methoxyethoxy)cinnoline as a white solid (87 mg, 44%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087602B2
出典データセットuspto-grants-2006_08
ORD IDord-3806cfe94ac247309d3610fb7b304642
出典メモuspto-grants-2006_08