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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899869Generated: October 25, 2026

1-Hydroxybenzotriazole → Methyl 2-{[(4-{2-[(2,4-difluorobenzyl)(heptyl)amino]-2-oxoethyl}phenyl)thio]methyl}benzoate

https://huagongshe.com/reaction/899869

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantN-(2,4-difluorobenzyl)-N-heptylamineHCID 60663854—
Reactant(4-{[2-(Methoxycarbonyl)benzyl]thio}phenyl)acetic acidHCID 69120445—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-{[(4-{2-[(2,4-difluorobenzyl)(heptyl)amino]-2-oxoethyl}phenyl)thio]methyl}benzoateHCID 6912060777.4%

Reaction Steps

(4-{[2-(Methoxycarbonyl)benzyl]thio}phenyl)acetic acid (581 mg, 1.836 mmol) and N-(2,4-difluorobenzyl)-N-heptylamine (465.3 mg, 1.968 mmol) were combined in DMF and the mixture was cooled in an ice-bath. HOBT (260.6 mg, 1.928 mmol) and TBTU (619 mg, 1.928 mmol) were added, followed by DIPEA (747.7 mg 5.785 mmol). The mixture was stirred at room temperature overnight and then evaporated. The resulting mixture was partitioned between ethyl acetate and sodium hydrogencarbonate aqueous solution (sat.). The aqueous portion was extracted with ethyl acetate and the combined organic extracts was dried with magnesium sulphate and then evaporated. Chromatography of the residue on a column (ISOLUTE® SI, 20 g/70 ml) using ethyl acetate/heptane (5:95, then 10:90) as eluant gave 767 mg the desired product, yield 77%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07355069B2
Source datasetuspto-grants-2008_04
ORD IDord-86778b2ba32f4adf8e46b31abd75301b
Source noteuspto-grants-2008_04