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HRID 395344作成日:2026年10月24日

Tetrahydrofuran → N-(4-Chloro-2-cyanophenyl)-2-(5-morpholin-4ylbenzimidazol-2-yl)acetamide

https://huagongshe.com/ja/reaction/395344

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物2-Amino-5-chlorobenzonitrileHCID 80019—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物Ethyl 2-[5-(2-morpholin-4-ylethoxy)benzimidazol-2-yl]acetateHCID 12988786—
生成物N-(4-Chloro-2-cyanophenyl)-2-(5-morpholin-4ylbenzimidazol-2-yl)acetamideHCID 22664809—

反応条件

温度23 °C

反応手順

LiHMDS (2.5 eq) was added to ethyl 2-[5-(2-morpholin-4-ylethoxy)benzimidazol-2-yl]acetate (1.0 eq) in THF at −78° C. After 1 hour, 2-amino-5-chlorobenzenecarbonitrile (0.82 eq) in THF was added. The reaction was allowed to warm to 23° C. and stirred overnight. The resulting mixture was quenched with NH4Cl (aqueous saturated solution) and extracted with EtOAc. The combined organic layers were washed with H2O and brine, dried over Na2SO4, filtered and concentrated in vacuo to yield a brown solid. The crude material was purified by silica gel chromatography (5:1 EtOAc:hexane) to give the desired product. LC/MS m/z 396.1 (MH+), Rf 1.79 minutes.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06605617B2
出典データセットuspto-grants-2003_08
ORD IDord-31fb1ab8829c49f191a7f1634835eb16
出典メモuspto-grants-2003_08