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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187367Generated: October 29, 2026

Tetrahydrofuran → 6-chloro-N-cyclohexyl-2-[2-(4-fluorophenyl)ethoxy]nicotinamide

https://huagongshe.com/reaction/1187367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-Fluorophenethyl AlcoholHCID 82068—
Reactant2,6-dichloro-N-cyclohexylnicotinamideHCID 52762493—
Solvent1,4-DioxaneHCID 31275—
Product6-chloro-N-cyclohexyl-2-[2-(4-fluorophenyl)ethoxy]nicotinamideHCID 5983068140.6%

Reaction Conditions

Temperature150 °C

Reaction Steps

2,6-dichloro-N-cyclohexylnicotinamide (Intermediate 1, 273 mg, 1 mmol) was stirred in 1,4-dioxane (4 ml). To this solution was added 4-fluorophenethyl alcohol (154 mg, 1.1 mmol) followed by bis-sodium hexamethyldisilylamide 1.0M in THF (1.1 ml, 1.1 mmol). The tube was sealed and subjected to microwave heating 150° C. (Biotage Initiator 300 W) for 2 hours. The solvent was evaporated and the residue was diluted with water (15 ml) and extracted with dichloromethane (2×20 ml). The combined extract was washed with brine (20 ml) dried over MgSO4, filtered and evaporated. The crude product was purified on SiO2 (40 g) eluting with ethyl acetate/isohexane 0-40% and gave 6-chloro-N-cyclohexyl-2-[2-(4-fluorophenyl)ethoxy]nicotinamide (153 mg, 40%) as a white solid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673938B2
Source datasetuspto-grants-2014_03
ORD IDord-4e93512bae9640d5acd6a18aef349882
Source noteuspto-grants-2014_03