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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843349Generated: October 29, 2026

Diisopropylethylamine → 1-(1-Tert-butoxycarbonylpiperidine-3-carbonyl)-piperidine-2-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide

https://huagongshe.com/reaction/843349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBOPHCID 2724699—
Reactant1-((Tert-butoxy)carbonyl)piperidine-3-carboxylic acidHCID 2735647—
Reactant2-[4-Phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]-piperidineHCID 12992460—
SolventDichloromethaneHCID 6344—
Product1-(1-Tert-butoxycarbonylpiperidine-3-carbonyl)-piperidine-2-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amideHCID 18727500—

Reaction Steps

Piperidine-2-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide (74) (1.00 g; 2.64 mmol) is dissolved in methylene chloride (25 mL) at ambient temperature. 1-tert-Butoxycarbonyl-piperidine-3-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 19 hours at room temperature, then concentrated under reduced pressure. The residue is purified via silica gel chromatography (30%→50% ethyl acetate in hexanes) affording the desired product (81) as a solid. ESMS: MH+ 590.6

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376514B1
Source datasetuspto-grants-2002_04
ORD IDord-b5cd31dc82a64d9e9dd4e38c347719f3
Source noteuspto-grants-2002_04