HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384106Generated: October 25, 2026
3-Aminophenol → 1-(3-Hydroxyanilino)-4-(4-pyridylmethyl)phthalazine
https://huagongshe.com/reaction/1384106
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Aminophenol | HCID 11568 | — |
| Reactant | 1-Chloro-4-(4-pyridinylmethyl)phthalazine | HCID 1944609 | — |
| Solvent | Acetate | HCID 175 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Product | 1-(3-Hydroxyanilino)-4-(4-pyridylmethyl)phthalazine | HCID 6419391 | — |
Reaction Steps
A mixture of 0.384 g (1.5 mmol) 1-chloro-4-(4-pyridylmethyl)phthalazine and 0.491 g (4.5 mmol) 3-aminophenol is heated under nitrogen atmosphere for 1 h at 90° C. and for 3 h at 120° C. The reaction mixture is then taken up in a mixture of 30 ml acetate and 20 ml 20% aqueous potassium carbonate solution while stirring for about 4 h, and the filtration material is digested for 20 min in 20 ml of boiling methanol. After cooling to RT, filtration, washing of the filter residue with methanol, and drying under HV (8 h, 130° C.), title compound is obtained with a water content of 1.94%; m.p. 217-219° C.; ESI-MS: (M+H)+=329.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06258812B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-aee4695973b343dca4b94d8387dcfc84 |
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| Source note | uspto-grants-2001_07 |
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