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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720907Generated: October 30, 2026

Diisopropylethylamine → 1-(1-Tert-butoxycarbonylpiperidine-4-carbonyl)-piperidine-4-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide

https://huagongshe.com/reaction/720907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
ReactantPyBOPHCID 2724699—
ReactantPiperidine-4-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amideHCID 12020260—
SolventDichloromethaneHCID 6344—
Product1-(1-Tert-butoxycarbonylpiperidine-4-carbonyl)-piperidine-4-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amideHCID 18727505—

Reaction Steps

Piperidine-4-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide (4) (1.00 g; 2.64 mmol) is dissolved in methylene chloride (25 mL) at ambient temperature. 1-tert-Butoxycarbonyl-piperidine-4-carboxylic acid (0.73 g; 3.17 mmol), N,N-diisopropylethylamine (0.75 g; 5.81 mmol) and PyBOP (1.65 g; 3.17 mmol) are added sequentially. The reaction is stirred for 16 hours at room temperature, then concentrated under reduced pressure. The residue is purified via silica gel chromatography (70%→90% ethyl acetate in hexanes) affording the desired product (70) as a solid. ESMS:MH+ 590.6

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135483B2
Source datasetuspto-grants-2006_11
ORD IDord-13b317db8b5847f781da2ef514b8471f
Source noteuspto-grants-2006_11