HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49906Generated: October 29, 2026
1-Chloro-4-(4-pyridinylmethyl)phthalazine → HCID 22741993, compound
https://huagongshe.com/reaction/49906
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Chloro-4-(4-pyridinylmethyl)phthalazine | HCID 1944609 | — |
| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Reactant | HCID 54200978 | HCID 54200978 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22741993 | HCID 22741993 | — |
Reaction Steps
To 262 mg (1.05 mmol) decyloxyaniline (Salor) in 5 ml ethanol, 0.26 ml HCl/dioxane 4N is added, the mixture stirred for 3 min, and then 256 mg (1.00 mmol) 1-chloro-4-(4-pyridylmethyl)phthalazine (Example 67A.1) is added. After 2 h boiling under reflux, the mixture is cooled and concentrated by evaporation. The residue is 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) and concentrated by evaporation. Crystallization [possibly after chromatography on SiO2 (ethyl acetate/CH3OH, 19:1)] from acetonitrile (or methanol) yields the title compound: m.p.: 116-119° C.; Anal. calc.(C30H36N4O) C, 76.89%; H, 7.74%; N, 11.96%. found C, 76.7%; H, 7.7%; N, 11.9%; FAB MS (M+H)+=469.
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-c0c1f6d3ae014cb7ba633e0d05b64d17 |
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| Source note | uspto-grants-2004_03 |
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