HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057722Generated: October 26, 2026
Ammonia → 1-(3-Phenoxyanilino)-4-(4-pyridylmethyl)phthalazine
https://huagongshe.com/reaction/1057722
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | (4-Aminophenoxy)benzene | HCID 8764 | — |
| Reactant | 1-Chloro-4-(4-pyridinylmethyl)phthalazine | HCID 1944609 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | 1-(3-Phenoxyanilino)-4-(4-pyridylmethyl)phthalazine | HCID 22742003 | — |
Reaction Steps
A mixture of 256 mg (1.00 mmol) 1-chloro-4-(4-pyridylmethyl)phthalazine and 556 mg (3.00 mmol) 4-phenoxyaniline (Aldrich) is heated for 2 h at 90° C. The melt is cooled and stirred with 6 ml NH3 solution (10% in water: or 10 ml sat. NaHCO3 solution) and 15 ml dichloromethane/methanol 50:1 for 30 min. The aqueous phase is then separated off and extracted again with dichloromethane. The organic phase is dried (Na2SO4), concentrated by evaporation, and chromatographed (SiO2; ethyl acetate→ethyl acetate/CH3OH, 19:1→10:1). Crystallization from acetonitrile yields the title compound: m.p.: 186-189° C.; Anal. calc. (C26H21N4O) C, 77.02%; H, 5.22%; N, 13.82%; found C, 77.2%; H, 4.9%; N, 13.8%. The starting material is prepared as follows:
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-ae489a8ae65d4ef0bb4ec17145bf7e5a |
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| Source note | uspto-grants-2003_02 |
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