HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057676Generated: October 25, 2026
1-Phenethylamine, (-)- → (S)-1-(1-Phenylethylamino)-4-(4-pyridylmethyl)phthalazine
https://huagongshe.com/reaction/1057676
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Phenethylamine, (-)- | HCID 75818 | — |
| Reactant | 1-Chloro-4-(4-pyridinylmethyl)phthalazine | HCID 1944609 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | (S)-1-(1-Phenylethylamino)-4-(4-pyridylmethyl)phthalazine | HCID 54550094 | — |
Reaction Steps
A mixture of 0.511 g (2 mmol) 1-chloro-4-(4-pyridylmethyl)phthalazine, 1.273 ml (10 mmol) (S)-1phenylethylamine and 5 ml 1-butanol is stirred for 24 h at 110° C. The reaction mixture is evaporated under vacuum and the residue distributed between dichloromethane and 20% aqueous potassium carbonate solution. The organic phase dried over anhydrous sodium sulfate is evaporated in the RE and then under HV and the residue purified on silica gel by flash chromatography using dichloromethane/methanol (50:1). The product-containing fractions are dissolved in 5 ml methanol, acidified with 0.75 ml 3N methanolic HCl and evaporated under vacuum. After recrystallization of the residue from methanol/acetonitrile, drying of the crystallizate under HV (8 h, 100° C.) and equilibration for 15 h at 20° C. and in room atmosphere, title compound is obtained with a water content of 10.66%; m.p. 190° C. (decomp.); ESI-MS: (M+H)+=341; [a]D20=+42.1±0.8° (c=1.272%, methanol).
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-75be70076af84794aef6e554d6af45e7 |
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| Source note | uspto-grants-2003_02 |
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