戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 49863作成日:2026年10月25日

1-Phenethylamine, (-)- → (S)-1-(1-Phenylethylamino)-4-(4-pyridylmethyl)phthalazine

https://huagongshe.com/reaction/49863

反応式

関与物質

役割名称HCID仕込み量
反応物1-Phenethylamine, (-)-HCID 75818—
反応物1-Chloro-4-(4-pyridinylmethyl)phthalazineHCID 1944609—
溶媒1-ButanolHCID 263—
生成物(S)-1-(1-Phenylethylamino)-4-(4-pyridylmethyl)phthalazineHCID 54550094—

反応条件

温度110 °C

反応手順

A mixture of 0.511 g (2 mmol) 1-chloro-4-(4-pyridylmethyl)phthalazine, 1.273 ml (10 mmol) (S)-1 phenylethylamine 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; [α]D20 =+42.1±0.8° (c=1.272%, methanol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710047B2
出典データセットuspto-grants-2004_03
ORD IDord-aba9693d37aa4c728072a9adba9d472f
出典メモuspto-grants-2004_03