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1,3-Benzenediamine, N1,N1-dimethyl-, hydrochloride (1:2) → 4-(3-Dimethylamino-phenylamino)-5,8-dimethoxy-quinoline-3-carbonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,3-Benzenediamine, N1,N1-dimethyl-, hydrochloride (1:2) | HCID 77124 | — |
| 反応物 | 1-Ethoxyethanol | HCID 10129898 | — |
| 反応物 | 4-Chloro-5,8-dimethoxyquinoline-3-carbonitrile | HCID 22466535 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | 4-(3-Dimethylamino-phenylamino)-5,8-dimethoxy-quinoline-3-carbonitrile | HCID 22466736 | 77.2% |
反応手順
A mixture of 0.148 g of 4-chloro-5,8-dimethoxy-3-quinolinecarbonitrile, 0.146 g of N,N-dimethyl-1,3-phenylenediamine dihydrochloride, 0.2 ml of pyridine, and 5 ml of ethoxyethanol was stirred under nitrogen, at reflux temperature for 30 minutes. Then the mixture was partitioned between ethyl acetate and saturated sodium chloride solution. The organic layer was dried and concentrated in vacuo. The residue thus obtained was chromatographed on silica gel eluting with ethyl acetate. Solvent was removed from product fractions giving 0.160 g of 4-(3-dimethylamino-phenylamino)-5,8-dimethoxy-quinoline-3-carbonitrile as a solid, mp 103-105° C.; mass spectrum (EI, m/e): M 348.1588.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06002008 |
| 出典データセット | uspto-grants-1999_12 |
| ORD ID | ord-9a9221bcd5094dbea5d4910619fe94c9 |
| 出典メモ | uspto-grants-1999_12 |