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HRID 1850850作成日:2026年10月27日

Triethylamine → N'-[2-({1-[1-(4-Chlorophenyl)cyclobutyl]-4,4-dimethyl-3,4-dihydroisoquinolin-7-yl}oxy)ethyl]-N,N-diethylsulfuric diamide

https://huagongshe.com/reaction/1850850

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物N,N-diethylsulfamoyl chlorideHCID 11252267—
反応物2-({1-[1-(4-Chlorophenyl)cyclobutyl]-4,4-dimethyl-3,4-dihydroisoquinolin-7-yl}oxy)ethanamineHCID 58246302—
溶媒DichloromethaneHCID 6344—
生成物N'-[2-({1-[1-(4-Chlorophenyl)cyclobutyl]-4,4-dimethyl-3,4-dihydroisoquinolin-7-yl}oxy)ethyl]-N,N-diethylsulfuric diamideHCID 66868671—

反応条件

温度2.5 °C

反応手順

2-({1-[1-(4-Chlorophenyl)cyclobutyl]-4,4-dimethyl-3,4-dihydroisoquinolin-7-yl}oxy)ethanamine (145 mg, 0.38 mmol, cf. example 67) was dissolved in dry dichloromethane (8 mL). Triethylamine (60 μL, 0.45 mmol). The solution was cooled to 0-5° C. and diethylsulfamoyl chloride (71.5 mg, 0.42 mmol) was added. The reaction mixture was stirred at room temperature over night. The reaction mixture was diluted with dichloromethane (20 mL) and washed with a 1:1 mixture of water and saturated ammonium chloride solution (20 mL). The organic layer was dried (MgSO4) and the solvent was evaporated in vacuo. The crude product was purified by flash chromatography (silica, dichloromethane then dichloromethane:ethyl acetate=180:5). Yield: 96 mg (0.19 mmol, 48.9%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08957089B2
出典データセットuspto-grants-2015_02
ORD IDord-42b2f3ce90a648c7b1166e2a0717bd11
出典メモuspto-grants-2015_02