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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534957Generated: October 31, 2026

Triethylamine → HCID 66792784, compound

https://huagongshe.com/reaction/534957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 61636743HCID 61636743—
Reactant1-(2-Tert-butylphenyl)piperazine dihydrochlorideHCID 66751149—
SolventAcetonitrileHCID 6342—
ProductHCID 66792784HCID 6679278437%

Reaction Steps

A mixture of 1-(2-tert-butylphenyl)piperazine dihydrochloride (Reference Example 1, 0.30 g, 1.03 mmol), 5-cyclohexyl-1,3-oxazole-4-carboxylic acid (Reference Example 14, 0.22 g, 1.13 mmol), triethylamine (0.23 g, 2.26 mmol), EDCI (0.22 g, 1.13 mmol) and HOBt (0.17 g, 1.13 mmol) in acetonitrile (10 mL) was stirred at room temperature for 16 h. The reaction mixture was concentrated under reduced pressure and the resulting residue was partitioned between ethyl acetate and 10% sodium hydrogen carbonate solution. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate 80:20 to 50:50) and the resulting white solid was triturated with hexane to give the title compound (0.15 g, 37%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-65d8367f98104760ad7196304c02b55a
Source noteuspto-grants-2014_10