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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898897Generated: October 30, 2026

Methyl Salicylate → Methyl 2-[2-(4-{2-[(2,4-difluorobenzyl)(heptyl)amino]-2-oxoethoxy}-3-methoxyphenyl)ethoxy]benzoate

https://huagongshe.com/reaction/898897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl SalicylateHCID 4133—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(4-{2-[(2,4-Difluorobenzyl)(heptyl)amino]-2-oxoethoxy}-3-methoxyphenyl)ethyl methanesulfonateHCID 86600966—
SolventAcetonitrileHCID 6342—
ProductMethyl 2-[2-(4-{2-[(2,4-difluorobenzyl)(heptyl)amino]-2-oxoethoxy}-3-methoxyphenyl)ethoxy]benzoateHCID 6925949051%

Reaction Steps

2-(4-{2-[(2,4-Difluorobenzyl)(heptyl)amino]-2-oxoethoxy}-3-methoxyphenyl)ethyl methanesulfonate (138 mg, 0.262 mmol) was dissolved in acetonitrile (10 ml). 2-Hydroxybenzoic acid methyl ester (40 mg, 0.262 mmol) was added and then potassium carbonate anhydrous (54 mg, 0.392 mmol) was added. The mixture was heated to reflux overnight and then evaporated to dryness. Water (10 ml) and ethyl acetate (10 ml) were added and the two phases were separated. The organic phase was washed with water and brine, dried (magnesium sulphate) and evaporated. Chromatography of the residue on a column (ISOLUTE® SI, 2 g/6 ml) using DCM, MeOH/DCM (1:99) as eluant gave 78 mg the desired product, yield 45% (two steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351858B2
Source datasetuspto-grants-2008_04
ORD IDord-b8e07327be2948228bbf0ffa856dddee
Source noteuspto-grants-2008_04