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HRID 47120作成日:2026年10月26日

N-Methylhomoveratrylamine → 7,7-Dimethyl-2-(4-chloro-phenyl)-5-[2-(N-methyl-N-(2-(3,4-dimethoxy-phenyl)-ethyl)-amino)-ethyl]-5H,7H-imidazo[4,5-h]-isoquinoline-4,6-dione dihydrochloride

https://huagongshe.com/reaction/47120

反応式

関与物質

役割名称HCID仕込み量
反応物N-MethylhomoveratrylamineHCID 77039—
反応物7,7-dimethyl-2-(4-chlorophenyl)-5-(2-chloro-ethyl)-5H,7H-imidazo[4,5-h]isoquinoline-4,6-dioneHCID 70610426—
溶媒ChloroformHCID 6212—
生成物7,7-Dimethyl-2-(4-chloro-phenyl)-5-[2-(N-methyl-N-(2-(3,4-dimethoxy-phenyl)-ethyl)-amino)-ethyl]-5H,7H-imidazo[4,5-h]-isoquinoline-4,6-dione dihydrochlorideHCID 70611007—

反応条件

温度150 °C

反応手順

A mixture consisting of 1.5 gm of 7,7-dimethyl-2-(4-chlorophenyl)-5-(2-chloro-ethyl)-5H,7H-imidazo[4,5-h]isoquinoline-4,6-dione and 1.7 gm of N-methyl-N-(2-(3,4-dimethoxy-phenyl)-ethyl)-amine was heated at 150° C. for 3 hours. After cooling the reaction mixture was dissolved in chloroform, and the solution was washed with water. The chloroform phase was evaporated, and the residue was chromatographed on a silicagel column (eluant: chloroform/acetone 19:1). The dihydrochloride was precipitated from acetone by addition of ethereal hydrochloric acid and recrystallized from methylene chloride/acetone.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04176184
出典データセットuspto-grants-1979_11
ORD IDord-72fb132aac154e7b92d6bf9be397eb96
出典メモuspto-grants-1979_11