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HRID 989332作成日:2026年10月25日

(4-Aminophenoxy)benzene → 4-(4-Phenoxyphenylamino)benzo[4,5]furo[3,2-b]pyridine-3-carbonitrile

https://huagongshe.com/reaction/989332

反応式

関与物質

役割名称HCID仕込み量
反応物(4-Aminophenoxy)benzeneHCID 8764—
反応物4-Chlorobenzo[4,5]furo[3,2-b]pyridine-3 carbonitrileHCID 9899399—
溶媒Glycol monoethyl etherHCID 8076—
生成物4-(4-Phenoxyphenylamino)benzo[4,5]furo[3,2-b]pyridine-3-carbonitrileHCID 1027092735%

反応手順

A mixture of 200 mg (0.88 mmol) of 4-chlorobenzo[4,5]furo[3,2-b]pyridine-3-carbonitrile and 180 mg (0.96 mmol) of 4-phenoxyaniline in 5 mL of 2-ethoxyethanol is heated at reflux temperature for 3 hours. The reaction mixture is cooled to room temperature and partitioned between ethyl acetate and saturated sodium bicarbonate. The organic layer is washed with saturated sodium bicarbonate, followed by brine, then dried over sodium sulfate and filtered through a pad of diatomaceous earth. Concentration in vacuo yields 115 mg (35%) of a beige solid, mp 175-179° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06638929B2
出典データセットuspto-grants-2003_10
ORD IDord-bd042e1ef94342ad852d3fcc52e5e18c
出典メモuspto-grants-2003_10