関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Aminobiphenyl | HCID 7102 | — |
| 反応物 | Triethylamine hydrochloride | HCID 11130 | — |
| 反応物 | Phosphorus oxide (P4O10) | HCID 14812 | — |
| 反応物 | Carbonate Ion | HCID 19660 | — |
| 反応物 | 4-(4-Pyridylmethyl)-1(2H)-phtalazinone | HCID 789954 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dichloromethane methanol | HCID 21226129 | — |
| 生成物 | N-(4-phenylphenyl)-4-(pyridin-4-ylmethyl)phthalazin-1-amine | HCID 6419389 | — |
反応手順
A mixture of 2.41 g (16.98 mmol) phosphorus pentoxide, 2.32 g (16.85 mmol) triethylamine hydrochloride, 3 g (17.73 mmol) 4-aminobiphenyl, and 1 g (4.21 mmol) 4-(4-pyridylmethyl)-1(2H)-phthalazinone is stirred for 20 h at 200° C. under a nitrogen atmosphere. After cooling to RT, the hyalinocrystalline melt is distributed between a dichloromethane/methanol mixture (99:1) and a mixture of water and saturated aqueous carbonate solution on (1:1) with intensive stirring and the use of an ultrasonic bath. The organic phase dried over sodium sulfate is evaporated under vacuum and the residue purified by means of flash chromatography on silica gel with particle size 0.04-0.06 mm, using a dichloromethane/methanol mixture (49:1). Title compound is obtained after evaporation of the product-containing fractions under vacuum and recrystallization of the residue from acetonitrile; m.p. 189-191 °C.; ESI-MS: (M+H)+=389.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06710047B2 |
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| 出典データセット | uspto-grants-2004_03 |
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| ORD ID | ord-68d8d685ff174f3fb8764293eccc5175 |
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| 出典メモ | uspto-grants-2004_03 |
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