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2-Toluidine hydrochloride → 1-(2-Methylphenyl)-6-methyl-2,3-dihydropyrrolo [3,2-c]cinnoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Toluidine hydrochloride | HCID 12484 | — |
| 反応物 | 4-Chloro-3-(2-chloroethyl)-8-methylcinnoline | HCID 20072762 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 1-(2-Methylphenyl)-6-methyl-2,3-dihydropyrrolo [3,2-c]cinnoline | HCID 20072757 | — |
反応手順
3-(2-Chloroethyl)-4-chloro-8-methylcinnoline (2.5 g, 0.01mol) and o-toluidine hydrochloride (1.4 g, 0.01 mol) in 1,4 dioxan (20 ml) were heated under reflux for 20 hours. The solvent was evaporated under reduced pressure to give an oil. The oil was partitioned between chloroform and dilute sodium carbonate solution and extracted further with chloroform (4×100 ml). The chloroform extracts were combined, dried over magnesium sulphate, filtered and evaporated to give an oil. The oil was purified by column chromatography using dichloromethane then chloroform as eluant. The solid obtained was recrystallized from diethyl ether/ dichloromethane to give the title compound, 0.6 g, m.p. 135-137°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04988695 |
| 出典データセット | uspto-grants-1991_01 |
| ORD ID | ord-7a2061e706aa463688322487297d07ec |
| 出典メモ | uspto-grants-1991_01 |