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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843344Generated: October 30, 2026

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

https://huagongshe.com/reaction/843344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
ReactantPyBOPHCID 2724699—
Reactant2-[4-Phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]-piperidineHCID 12992460—
SolventDichloromethaneHCID 6344—
Product1-(1-Tert-butoxycarbonylpiperidine-4-carbonyl)-piperidine-2 carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amideHCID 18727503—

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-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 (30%→50% ethyl acetate in hexanes) affording the desired product (75) as a solid. ESMS: MH+ 590.6

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376514B1
Source datasetuspto-grants-2002_04
ORD IDord-bcba7d5d386d4774bd79666d9a05142a
Source noteuspto-grants-2002_04