Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278186Generated: October 31, 2026

1,2-Dichloroethane → 2-{5-[1-(4-cyano-3-fluorophenyl)-1-hydroxyethyl]imidazol-1-yl}-N-[2-(3'-hydroxybiphenyl-2-yl)ethyl]acetamide

https://huagongshe.com/reaction/278186

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantLithiumHCID 3028194—
Reactant{5-[1-(4-Cyano-3-fluorophenyl)-1-hydroxyethyl]imidazol-1-yl}acetic acidHCID 18433492—
Reactant1-Amino-2-(3'-hydroxybiphenyl-2-yl)ethaneHCID 22627086—
Product2-{5-[1-(4-cyano-3-fluorophenyl)-1-hydroxyethyl]imidazol-1-yl}-N-[2-(3'-hydroxybiphenyl-2-yl)ethyl]acetamideHCID 22627089—

Reaction Steps

A solution of {5-[1-(4-cyano-3-fluorophenyl)-1-hydroxyethyl]imidazol-1-yl}acetic acid, lithium salt from Step H (40 mg, 0.145 mmol), 1-amino-2-(3′-hydroxybiphenyl-2-yl)ethane from Example 6, Step C (33 mg, 0.155 mmol), 1-hydroxybenzotriazole hydrate (23 mg, 0.17 mmol), EDC (33 mg, 0.17 mmol), and N,N-diisopropylethylamine (40 mg, 0.31 mmol) in dry, degassed DMF (1 mL) was stirred at ambient temperature for 18 hrs. The solvent was removed under reduced pressure and the residue was partitioned between sat. aq. NaHCO3 (1 mL) and CHCl3 (3 mL). The aqueous layer was extracted further with CHCl3 (2×2 mL). The combined organic extracts were dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude product was purified by preparative thin layer chromatography, eluting with 6% MeOH/0.6% NH4OH in CH2Cl2 to give the titled product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358985B1
Source datasetuspto-grants-2002_03
ORD IDord-b800d3e8c43f40e8aa95bdd84415451c
Source noteuspto-grants-2002_03