Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883926Generated: October 26, 2026

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

https://huagongshe.com/reaction/1883926

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+), Rt 1.79 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06762194B2
Source datasetuspto-grants-2004_07
ORD IDord-ee75b53d91664d5d938cc736289afa5f
Source noteuspto-grants-2004_07