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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534948Generated: October 30, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → Methyl 1-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}piperidine-4-carboxylate

https://huagongshe.com/reaction/534948

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantMethyl isonipecotateHCID 424914—
ReactantSodium BicarbonateHCID 516892—
Reactant2-[4-(2-Tert-butylphenyl)piperazin-1-yl]-2-oxoacetic acidHCID 66750854—
SolventAcetonitrileHCID 6342—
ProductMethyl 1-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}piperidine-4-carboxylateHCID 6675115940.4%

Reaction Steps

A solution of [4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetic acid (Example 44, 0.300 g, 1.03 mmol), methyl piperidine-4-carboxylate (0.178 g, 1.24 mmol), EDCI (0.238 g, 1.24 mmol) and HOBt (0.168 g, 1.24 mmol) in acetonitrile (10 mL) was stirred at room temperature for 2 days. The reaction mixture was poured into saturated sodium hydrogen carbonate solution and extracted with ethyl acetate. The organic layer was washed with saturated sodium hydrogen carbonate solution and brine, dried over MgSO4, and the solvent was evaporated in vacuum to give the crude product. The product was purified by flash column chromatography (silica gel, n-hexane/ethyl acetate=90:10 to 50:50) to provide methyl 1-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}piperidine-4-carboxylate (0.173 g, 40%) as a white amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-d0305f1ae63b4d09b7b70300ad4de134
Source noteuspto-grants-2014_10