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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520261Generated: October 31, 2026

1-Hydroxybenzotriazole → ethyl (3R)-1-(4-((1-(4-(5-ethylpyrimidin-2-yl)-2-methylphenyl)-4,4,4-trifluorobutyl)amino)benzoyl)piperidine-3-carboxylate

https://huagongshe.com/reaction/1520261

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactantethyl (3R)-piperidine-3-carboxylateHCID 185582—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-((1-(4-(5-Ethylpyrimidin-2-yl)-2-methylphenyl)-4,4,4-trifluorobutyl)amino)benzoic acidHCID 117840030—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Productethyl (3R)-1-(4-((1-(4-(5-ethylpyrimidin-2-yl)-2-methylphenyl)-4,4,4-trifluorobutyl)amino)benzoyl)piperidine-3-carboxylateHCID 131733101—

Reaction Steps

A solution of 4-((1-(4-(5-ethylpyrimidin-2-yl)-2-methylphenyl)-4,4,4-trifluorobutyl)amino)benzoic acid obtained in step B, ethyl (3R)-piperidine-3-carboxylate (5.08 mL), 1-hydroxybenzotriazole (4.46 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (6.32 g) and diisopropylethylamine (5.76 mL) in dimethylformamide (79 mL) was stirred at room temperature overnight. The reaction mixture was added to water, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (15.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073864B2
Source datasetuspto-grants-2015_07
ORD IDord-9c46e9e3e5f1462999a64d4af2eba75c
Source noteuspto-grants-2015_07