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HRID 1387091作成日:2026年10月27日

Sodium Hydroxide → 6-Benzyloxy-2-dimethylaminobenzo[b]thiophen-3-yl 3-Methoxy-4-[(1-pyrrolidinyl)methyl]phenyl Ketone

https://huagongshe.com/reaction/1387091

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物6-Benzyloxy-2-dimethylaminobenzo[b]thiopheneHCID 10612994—
反応物3-Methoxy-4-[(1-pyrrolidinyl)methyl]benzoyl chlorideHCID 21706353—
溶媒ChlorobenzeneHCID 7964—
溶媒Sodium chloride; waterHCID 57417360—
生成物6-Benzyloxy-2-dimethylaminobenzo[b]thiophen-3-yl 3-Methoxy-4-[(1-pyrrolidinyl)methyl]phenyl KetoneHCID 1067301284%

反応手順

A solution of 6-benzyloxy-2-(dimethylamino)benzo[b]thiophene (2.5 g, 8.8 mmol) and 3-methoxy-4-[(1-pyrrolidinyl)methyl]benzoyl chloride (3.0 g, 1.3 equiv) in chlorobenzene (30 mL) was heated at 135° C. under nitrogen for 2 h. The cooled reaction mixture was diluted with brine (100 mL), neutralized with NaOH solution (5.0 M), and extracted with dichloromethane (100 mL×3). The combined organic layers were dried with sodium sulfate and concentrated under reduced pressure. Chromatography with Et3N:EtOAc (5:95) afforded the product as a brown oil (3.7 g, 84%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06265575B1
出典データセットuspto-grants-2001_07
ORD IDord-5e96b6e0ef1b4c77ae2c29d8b72c03eb
出典メモuspto-grants-2001_07