HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49884Generated: October 26, 2026
3-Chloro-4-fluoroaniline → 1-(3-Chloro-4-fluoroanilino)-4-(4-pyridylmethyl)phthalazine
https://huagongshe.com/reaction/49884
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloro-4-fluoroaniline | HCID 9708 | — |
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | 4-(4-Pyridylmethyl)-1(2H)-phtalazinone | HCID 789954 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(3-Chloro-4-fluoroanilino)-4-(4-pyridylmethyl)phthalazine | HCID 9799193 | — |
Reaction Steps
A mixture of 1.42 g (10 mmol) phosphorus pentoxide, 1.38 g (10 mmol) triethylamine hydrochloride, and 1.46 g (10 mmol) 3-chloro-4-fluoroaniline is heated and stirred in a nitrogen atmosphere at 200° C. until a homogeneous melt has formed. To the melt, 0.593 g (2.5 mmol) 4-(4-pyridylmethyl)-1(2H)-phthalazinone is added and the reaction mixture stirred for a further 3 h at 200° C. After cooling to RT, the hyalinocrystalline reaction mixture is distributed between 150 ml dichloromethane and a mixture of 10 ml water and 20 ml 2N sodium hydroxide solution with intensive stirring and sonication. The organic phase washed with water and dried over sodium sulfate is concentrated by evaporation and the residue recrystallized from acetate. Title compound is obtained after a second recrystallization from methanol/water and drying under HV (8 h at 100° C.); m.p. 185-187° C.; ESI-MS: (M+H)+=365.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06710047B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-8dbc3bce22d84d228a83e727e949ad00 |
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| Source note | uspto-grants-2004_03 |
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