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HRID 503653作成日:2026年10月25日
Dimethyl Sulfoxide → N-(4-(7-(benzyloxy)-1,5-naphthyridin-4-yloxy)phenyl)-4-(4-chlorophenyl)phthalazin-1-amine
https://huagongshe.com/reaction/503653
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Dimethyl Sulfoxide | HCID 679 | — |
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | 3-(Benzyloxy)-8-chloro-1,5-naphthyridine | HCID 67316944 | — |
| 反応物 | 4-(4-(4-Chlorophenyl)phthalazin-1-ylamino)phenol hydrochloride | HCID 136381728 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | N-(4-(7-(benzyloxy)-1,5-naphthyridin-4-yloxy)phenyl)-4-(4-chlorophenyl)phthalazin-1-amine | HCID 67316920 | — |
反応手順
A pyrex reaction tube was charged with 4-(4-(4-chlorophenyl)phthalazin-1-ylamino)phenol hydrochloride (344 mg, 894 μmol), 3-(benzyloxy)-8-chloro-1,5-naphthyridine (220 mg, 813 μmol), cesium carbonate (662 mg, 2032 μmol) and 4.1 mL DMSO. The tube was sealed and the mixture was heated at 100° C. for 4 h. Water was added and the resulting precipitate was filtered, washed with water and dried. The crude material was purified by silica gel chromatography, 90/10/1 DCM/MeOH/NH4OH in DCM to provide N-(4-(7-(benzyloxy)-1,5-naphthyridin-4-yloxy)phenyl)-4-(4-chlorophenyl)phthalazin-1-amine. MS: [M+H]=583.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07776857B2 |
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| 出典データセット | uspto-grants-2010_08 |
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| ORD ID | ord-2401d654fa9e4e1e8b6dd2a2f299cb59 |
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| 出典メモ | uspto-grants-2010_08 |
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