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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610774Generated: October 31, 2026

Benzylethanolamine → N-cyclohepty-5-[benzyl(2-hydroxyethyl)amino]pentanamide

https://huagongshe.com/reaction/610774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylethanolamineHCID 4348—
ReactantPotassium CarbonateHCID 11430—
Reactantn-Cycloheptyl-5-bromopentanamideHCID 22125969—
SolventDimethylformamideHCID 6228—
ProductN-cyclohepty-5-[benzyl(2-hydroxyethyl)amino]pentanamideHCID 2212597258.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

N-cycloheptyl-5-bromopentanamide (4.15 g, 15 mmole) in solution in dimethylformamide (20 ml) is added dropwise to a hot solution (60° C.) of N-benzylethanolamine (2.27 g, 2.13 ml, 15 mmole) in dimethylformamide (25 ml) in the presence of potassium carbonate (4.15 g, 3 mmole). The reaction mixture is agitated for 2 hours at 60° C. then the solvent is evaporated under reduced pressure. The residue is taken up in dichloromethane (50 ml) and washed with water (3×30 ml). The organic phase is collected, dried over magnesium sulfate; the solvent is evaporated under reduced pressure. The product obtained is purified by flash chromatography over silica gel in a mixture of dichloromethane/methanol (90/10) to give 3.04 g (50%) of the expected compound in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998666
Source datasetuspto-grants-1999_12
ORD IDord-fadcc4f3ec5f43bab5e96e01299add98
Source noteuspto-grants-1999_12