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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | N-Methylhomoveratrylamine | HCID 77039 | — |
| 反応物 | 7,7-dimethyl-2-(4-chlorophenyl)-5-(2-chloro-ethyl)-5H,7H-imidazo[4,5-h]isoquinoline-4,6-dione | HCID 70610426 | — |
| 溶媒 | Chloroform | HCID 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 dihydrochloride | HCID 70611007 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04176184 |
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| 出典データセット | uspto-grants-1979_11 |
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| ORD ID | ord-72fb132aac154e7b92d6bf9be397eb96 |
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| 出典メモ | uspto-grants-1979_11 |
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