HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057709Generated: October 25, 2026
4-Aminobiphenyl → N-(4-phenylphenyl)-4-(pyridin-4-ylmethyl)phthalazin-1-amine
https://huagongshe.com/reaction/1057709
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Aminobiphenyl | HCID 7102 | — |
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | Carbonate Ion | HCID 19660 | — |
| Reactant | 4-(4-Pyridylmethyl)-1(2H)-phtalazinone | HCID 789954 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | N-(4-phenylphenyl)-4-(pyridin-4-ylmethyl)phthalazin-1-amine | HCID 6419389 | — |
Reaction Steps
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 (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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06514974B2 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-383323b6e4fb4916aaabfa63371d3f2f |
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| Source note | uspto-grants-2003_02 |
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