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HRID 714064作成日:2026年10月25日

Methanol → (rac)-N-[4-(4-Cyanophenyl)-5,6,7,8-tetrahydroisoquinolin-8-yl]-N'-propylsulfuric diamide

https://huagongshe.com/reaction/714064

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物TriethylamineHCID 8471—
反応物N-propylsulfamoyl chlorideHCID 13398949—
反応物4-(8-Amino-5,6,7,8-tetrahydro-4-isoquinolinyl)benzonitrileHCID 71811360—
溶媒DichloromethaneHCID 6344—
生成物(rac)-N-[4-(4-Cyanophenyl)-5,6,7,8-tetrahydroisoquinolin-8-yl]-N'-propylsulfuric diamideHCID 7181136268%

反応手順

A cooled (0° C.) solution of (rac)-4-(8-amino-5,6,7,8-tetrahydroisoquinolin-4-yl)benzonitrile (example 1) (62.3 mg, 250 μmol) in CH2Cl2 (3 ml) was treated with propylsulfamoyl chloride (98.5 mg, 625 μmol) in CH2Cl2 (0.6 ml) and Et3N (69.7 μL, 500 μmol). After 1 h the mixture was stirred at room temperature for 1 h, cooled down (0° C.) and treated again with Et3N (69.7 μL, 500 μmol). After ½ h at room temperature, the mixture was treated with MeOH (0.2 mL) and extracted with water/AcOEt (3×). The organic phases were dried over Na2SO4, filtered and evaporated under reduced pressure. Purification by flash chromatography (50 g SiO2, Telos-cartridge, CH2Cl2/MeOH (1 to 3%)) and precipitation from CH2Cl2 with n-pentane gave the title compound (63 mg, 68%) as off-white powder. MS: 371.2 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09187429B2
出典データセットuspto-grants-2015_11
ORD IDord-beee2114ca484373af676d4505643951
出典メモuspto-grants-2015_11