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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535020Generated: October 31, 2026

Triethylamine → HCID 66751357, compound

https://huagongshe.com/reaction/535020

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 66590087HCID 66590087—
Reactant1-(2-Tert-butylphenyl)piperazine dihydrochlorideHCID 66751149—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 66751357HCID 6675135787%

Reaction Steps

A mixture of 1-(2-tert-butylphenyl)piperazine dihydrochloride obtained in Reference Example 1 (1.0 g, 3.43 mmol), 4-{[1-(tert-butoxycarbonyl)piperidin-4-yl]methoxy}benzoic acid (1.41 g, 4.2 mmol), triethylamine (1.53 mL, 11.0 mmol), EDCI (0.824 g, 4.3 mmol) and HOBt (0.659 g, 4.3 mmol) in N,N-dimethylformamide (10 mL) was stirred at room temperature for 16 h. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to purify the residue by NH-silica gel column chromatography (hexane/ethyl acetate 10:90 to 0:100). Solvent was removed to obtain a solid (1.6 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-370587b5cf014ec3adba6ce520da5b46
Source noteuspto-grants-2014_10