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HRID 45197作成日:2026年10月25日

Cesium carbonate → {1-[4-(Isoquinolin-6-ylamino)-1-(4-methoxy-phenyl)-cyclohexyl]-propyl}-carbamic acid benzyl ester

https://huagongshe.com/reaction/45197

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物6-BromoisoquinolineHCID 313681—
反応物Binap, (A+-)-HCID 634876—
反応物{1-[4-Amino-1-(4-methoxy-phenyl)-cyclohexyl]-propyl}carbamic acid benzyl esterHCID 58380970—
触媒palladium(II) acetateHCID 167845—
溶媒TolueneHCID 1140—
生成物{1-[4-(Isoquinolin-6-ylamino)-1-(4-methoxy-phenyl)-cyclohexyl]-propyl}-carbamic acid benzyl esterHCID 6707563028.6%

反応条件

温度100 °C

反応手順

In 1 mL of absolute toluene were dissolved 66.0 mg (0.32 mmol) of 6-bromo-isoquinoline, 151 mg (380 μmol) of {1-[4-amino-1-(4-methoxy-phenyl)-cyclohexyl]-propyl}-carbamic acid benzyl ester (98), and 155 mg (476 μmol) of cesium carbonate. The solution was degassed twice, then 2.14 mg (9.5 μmol) of palladium acetate and 8.89 mg (14.3 μmol) of 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl were added and the reaction mixture was heated to 100° C. until complete conversion could be observed. The mixture was evaporated, then redissolved in 50 mL of dichloromethane and washed twice with 50 mL of saturated aqueous sodium bicarbonate solution. The organic phase was dried over magnesium sulphate, filtered, concentrated and purified by silica gel chromatography (dichloromethane:methanol) to give 48 mg of the pure desired product. Rt=1.38 min (Method 19). Detected mass: 524.4 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541449B2
出典データセットuspto-grants-2013_09
ORD IDord-c82a7faf1ea04e85bdff193acf86afb6
出典メモuspto-grants-2013_09