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HRID 54758作成日:2026年10月26日

Sodium Iodide → 5-(2-cyanomethylaminoethoxy)-7-chloro-1-[2-methoxy-4-(2-chlorobenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzo-azepine

https://huagongshe.com/reaction/54758

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物ChloroacetonitrileHCID 7856—
反応物TriethylamineHCID 8471—
反応物5-(2-aminoethoxy)-7-chloro-1-[2-methoxy-4-(2-chlorobenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzoazepineHCID 18917210—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物5-(2-cyanomethylaminoethoxy)-7-chloro-1-[2-methoxy-4-(2-chlorobenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzo-azepineHCID 53719122—

反応条件

温度60 °C

反応手順

0.01 ml of chloroacetonitrile, 0.22 ml of triethylamine and 0.24 ml of sodium iodide were added to 50 ml of a solution of 0.7 g of 5-(2-aminoethoxy)-7-chloro-1-[2-methoxy-4-(2-chlorobenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzoazepine dissolved in dimethylformamide. The mixture was stirred at 60° C. for 2 hours. The reaction mixture was mixed with water, followed by extraction with ethyl acetate-n-hexane (10:1). The organic layer was water-washed, dried and subjected to vacuum distilation to remove the solvent. The residue was purified by silica gel column chromatography (elutant: dichloromethane/methanol=50/1) and crystallized from acetone-n-hexane to obtain 0.5 g of 5-(2-cyanomethylaminoethoxy)-7-chloro-1-[2-methoxy-4-(2-chlorobenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzo-azepine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05622947
出典データセットuspto-grants-1997_04
ORD IDord-1e51edf5b77046b28bfbebbd9e96e5e4
出典メモuspto-grants-1997_04