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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330070Generated: October 25, 2026

Ethanamine, 2-fluoro-, hydrochloride → N-(2-chloroethyl)-(3-benzyl-5,6-diethylpyrazine-2-yl oxy) acetamide

https://huagongshe.com/reaction/330070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanamine, 2-fluoro-, hydrochlorideHCID 9995—
ReactantPotassium CarbonateHCID 11430—
ReactantPivaloyl chlorideHCID 62493—
Reactant(3-Benzyl-5,6-diethylpyrazine-2-yl oxy) acetateHCID 86743689—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductN-(2-chloroethyl)-(3-benzyl-5,6-diethylpyrazine-2-yl oxy) acetamideHCID 1517045188.8%

Reaction Steps

Pivaloyl chloride (3.66 g, 30 mM) was added dropwise at -5° C. to compound 655 (8.62 g, 28.7 mM) and triethylamine (4.2 ml, 30 mM) dissolved in tetrahydrofuran (50 ml), then the mixture was stirred for 30 minutes. Chloroform (30 ml) in solution with 2-fluoroethylamine hydrochloride (3.48 g) and triethylamine (4.2 ml) was added dropwise thereto with cooling at 0° to -5° C. then the mixture was stirred for 1 hour with ice cooling and 4 hours at room temperature. Dilute aqueous potassium carbonate was added to the reaction mixture and the mixture was extracted three times with chloroform. The extract was dried with anhydrous magnesium sulfate, and concentrated in vacuo. The residue was charged on a column of silica gel (C-200, 175 g) and eluted successively with benzene and benzene-ethyl acetate (5:1) to obtain the product. (9.21 g, yield: 88.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04894453
Source datasetuspto-grants-1990_01
ORD IDord-fd7256a37c514635bd620f41b69d38a7
Source noteuspto-grants-1990_01