戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 250333作成日:2026年10月25日

Methanol → 4-Hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid butyl ester

https://huagongshe.com/reaction/250333

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Sodium AcetateHCID 517045—
反応物Butyl 1-bromo-4-hydroxy-7-phenoxyisoquinoline-3-carboxylateHCID 86595463—
触媒PalladiumHCID 23938—
溶媒Ethyl AcetateHCID 8857—
生成物4-Hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid butyl esterHCID 6671295177.1%

反応手順

A mixture of 208 mg of 1-Bromo-4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid butyl ester (0.5 mmol), 49 mg of sodium acetate (0.6 mmol), 50 mg of 10 wt % palladium on charcoal, 10 ml of methanol, and 5 ml of ethyl acetate was stirred under hydrogen at 1 atm for 15 h. Then the mixture was filtered by suction through a pad of celite and was concentrated in vacuo. The residue was partitioned between 2 ml of half concentrated aqueous bicarbonate solution and 8 ml of ethyl acetate. The organic phase was dried over MgSO4. Evaporation in vacuo gave 130 mg of the title compound; 1H NMR (CDCl3): δ=11.89 (bs, 1H), 8.61 (s, 1H), 8.36 (d, 1H), 7.10 to 7.53 (m, 7H), 4.49 (t, 2H), 1.87 (m, 2H), 1.47 (m, 2H), 0.98 (t, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07863292B2
出典データセットuspto-grants-2011_01
ORD IDord-042a36b26f354773aa7be5d784819031
出典メモuspto-grants-2011_01