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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968702Generated: October 29, 2026

Diisopropylethylamine → 4-[4-Phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/968702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
ReactantPyBOPHCID 2724699—
Reactant1,7-Diphenyl-4-aminoheptane hydrochlorideHCID 21892255—
SolventDichloromethaneHCID 6344—
Product4-[4-Phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl esterHCID 12136744—

Reaction Steps

1-tert-Butoxycarbonyl-piperidine-4-carboxylic acid (4.00 g; 17.4 mmol) is dissolved in methylene chloride (125 mL) at ambient temperature. 1,7-Diphenyl-4-aminoheptane hydrochloride (1) (6.36 g; 20.9 mmol), diisopropylethylamine (7.27 g; 55.8 mmol), and PyBOP (10.89 g; 20.9 mmol) are added sequentially. The mixture is stirred for 14 hours at ambient temperature then concentrated in vacuo at 40° C. The residue is purified via silica gel chromatography with gradient elution (20%→40% ethyl acetate in hexanes) affording the desired product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07304053B2
Source datasetuspto-grants-2007_12
ORD IDord-490bd5b311c64e2f82da0dacdd745b61
Source noteuspto-grants-2007_12