戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1384146作成日:2026年10月27日

Ammonia → 1-(3-Phenoxyanilino)-4-(4-pyridylmethyl)phthalazine

https://huagongshe.com/reaction/1384146

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物(4-Aminophenoxy)benzeneHCID 8764—
反応物1-Chloro-4-(4-pyridinylmethyl)phthalazineHCID 1944609—
溶媒Dichloromethane methanolHCID 21226129—
生成物1-(3-Phenoxyanilino)-4-(4-pyridylmethyl)phthalazineHCID 22742003—

反応条件

温度90 °C

反応手順

A mixture of 256 mg (1.00 mmol) 1-chloro-4-(4-pyridylmethyl)phthalazine and 556 mg (3.00 mmol) 4-phenoxyaniline (Aldrich) is heated for 2 h at 90° C. The melt is cooled and 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), concentrated by evaporation, and chromatographed (SiO2; ethyl acetate→ethyl acetate/CH3OH 19:1→10:1). Crystallization from acetonitrile yields the title compound: m.p.: 186-1 89° C.; Anal. calc. (C26H21N4O) C 77.02%, H 5.22%, N 13.82%; found C 77.2%, H 4.9%, N 13.8%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06258812B1
出典データセットuspto-grants-2001_07
ORD IDord-e4af79b0d7b34a93a608936e1f118b90
出典メモuspto-grants-2001_07