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HRID 217527作成日:2026年10月25日

Ethanol → Methyl [3,5-bis(trifluoromethyl)benzyl][2-isoquinolin-4-yl-5-(trifluoromethyl)benzyl]carbamate

https://huagongshe.com/reaction/217527

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Sodium CarbonateHCID 10340—
反応物Isoquinoline-4-boronic acidHCID 3761204—
反応物Methyl [3,5-bis(trifluoromethyl)benzyl](2-iodo-5-trifluoromethyl-benzyl)carbamateHCID 59343876—
溶媒TolueneHCID 1140—
生成物Methyl [3,5-bis(trifluoromethyl)benzyl][2-isoquinolin-4-yl-5-(trifluoromethyl)benzyl]carbamateHCID 11563310—

反応条件

温度97.5 °C

反応手順

To a solution of methyl [3,5-bis(trifluoromethyl)benzyl](2-iodo-5-trifluoromethyl-benzyl)carbamate (41 mg, 0.070 mmol) (Example 5) in 3:2 EtOH:toluene, 4-isoquinolineboronic acid (18.2 mg, 0.105 mmol) and 2.5 M sodium carbonate (0.175 mmol) were added. The solution was degassed, followed by the addition of a catalytic amount of tetrakis(triphenylphosphine)palladium. The solution was stirred at 95-100° C. until completion of the reaction. Upon cooling, the solvent was removed in vacuo. The desired product was obtained by preparative thin layer chromatography using 25% acetone/hexane. 1H NMR (CDCl3, 500 MHz) δ 9.36 (s, 1H), 8.38 (s, 1H), 8.10-8.13 (m, 1H), 7.68-7.80 (m, 4H), 7.26-7.64 (m, 5H), 4.22-4.48 (m, 4H), 3.64-3.78 (m, 3H). LC-MS (M+1) 587.2 (3.48 min).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193365B2
出典データセットuspto-grants-2012_06
ORD IDord-14ce06d31f2c4c2db7a2fe467f7dd5af
出典メモuspto-grants-2012_06