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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395344Generated: October 26, 2026

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

https://huagongshe.com/reaction/395344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2-Amino-5-chlorobenzonitrileHCID 80019—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantEthyl 2-[5-(2-morpholin-4-ylethoxy)benzimidazol-2-yl]acetateHCID 12988786—
ProductN-(4-Chloro-2-cyanophenyl)-2-(5-morpholin-4ylbenzimidazol-2-yl)acetamideHCID 22664809—

Reaction Conditions

Temperature23 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605617B2
Source datasetuspto-grants-2003_08
ORD IDord-31fb1ab8829c49f191a7f1634835eb16
Source noteuspto-grants-2003_08