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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 395344생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물2-Amino-5-chlorobenzonitrileHCID 80019—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물Ethyl 2-[5-(2-morpholin-4-ylethoxy)benzimidazol-2-yl]acetateHCID 12988786—
생성물N-(4-Chloro-2-cyanophenyl)-2-(5-morpholin-4ylbenzimidazol-2-yl)acetamideHCID 22664809—

반응 조건

온도23 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06605617B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-31fb1ab8829c49f191a7f1634835eb16
출처 메모uspto-grants-2003_08