HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384100Generated: October 26, 2026
4-Aminoacetanilide → 1-(4-Acetaminoanilino)-4-(4-pyridylmethyl)phthalazine
https://huagongshe.com/reaction/1384100
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Aminoacetanilide | HCID 31230 | — |
| Reactant | 1-Chloro-4-(4-pyridinylmethyl)phthalazine | HCID 1944609 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 1-(4-Acetaminoanilino)-4-(4-pyridylmethyl)phthalazine | HCID 22741957 | — |
Reaction Steps
A mixture of 0.511 g (2 mmol) 1-chloro-4-(4-pyridylmethyl)phthalazine, 0.901 g (6 mmol) 4-aminoacetanilide and 5 ml 1-butanol is heated for 3 h at 110° C. The reaction mixture is then evaporated under vacuum, the crystalline residue is taken up in a mixture of 20 ml dichloromethane and 10 ml 20% aqueous potassium carbonate solution while stirring, then filtered and the filter residue washed with water and dichloromethane. After recrystallization from dichloromethane/methanol and drying under HV (8 h, 1 00° C.), title compound is obtained with a methanol content of 1.27%;
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-b0ff465855ba470f8a076567ba42a96b |
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| Source note | uspto-grants-2001_07 |
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