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4-Chloroaniline → 1-(4-Chloroanilino)phthalazine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Chloroaniline | HCID 7812 | — |
| 反応物 | 1(2H)-Phthalazinone | HCID 8394 | — |
| 反応物 | 1-Chlorophthalazine | HCID 160793 | — |
| 溶媒 | 1-Butanol | HCID 263 | — |
| 生成物 | 1-(4-Chloroanilino)phthalazine | HCID 22741997 | — |
反応手順
30 g (149 mmol) 1-chlorophthalazine (prepared from phthalazone in the manner described under Example 67A.1) and 20 g (157 mmol) 4-chloroaniline are heated in 630 ml n-butanol for 30 min to 65° C. The crude product is filtered off, washed with ether, taken up in 2 l dichloromethane/methanol 9:1, and washed with sat. NaHCO3 solution and brine. The aqueous phases are extracted three times with dichloromethane/methanol 9:1, the organic phases dried (Na2SO4), and evaporated to a residual volume of −50 ml, leading to crystallization of the title compound: m.p.: 211° C.; Anal. calc. (C14H10N3Cl) C 65.76%, H 3.94%, N 16.43%, Cl 13.86%; found C 66.02%, H 3.92%, N 16.53%, Cl 13.51%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06258812B1 |
| 出典データセット | uspto-grants-2001_07 |
| ORD ID | ord-45171c2b6a004f86bd1ba4dac95f215e |
| 出典メモ | uspto-grants-2001_07 |