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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549317Generated: October 26, 2026

Dicyclohexylcarbodiimide → (RS)-2-(5-Phenyl-[1,3,4]oxadiazol-2-ylmethyl)-piperidine-1-carboxylic acid tert butyl ester

https://huagongshe.com/reaction/549317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-Boc-2-Piperidineacetic AcidHCID 5058536—
ReactantHCID 178418369HCID 178418369—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product(RS)-2-(5-Phenyl-[1,3,4]oxadiazol-2-ylmethyl)-piperidine-1-carboxylic acid tert butyl esterHCID 8662899664.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-carboxymethyl-piperidine-1-carboxylic acid tert butyl ester (1.22 g), (Peschke, Bernd, Ankersen, Michael; Hansen, Birgit Sehested; Hansen, Thomas Kruse; Johansen, Nils Langeland, Lau, Jesper; Madsen, Kjeld, Petersen, Hans; Thogersen, Henning; Watson, Brett. Eur. J. Med. Chem. (1999), 34(5), 363-380), dicyclohexylcarbodiimide (1.05 g) and 5-phenyltetrazole (0.73 g) in toluene (25 ml) was heated at 100° C. for 3 h. The reaction mixture was cooled to room temperature, diluted with diethyl ether and solvent decanted from the precipitated gum. The gum was column chromatographed (silica gel, 0-50% ethyl acetate in pentane eluant) to give the title compound (1.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943645B2
Source datasetuspto-grants-2011_05
ORD IDord-adbfd1b97f7246b9a1edc3c760383e5c
Source noteuspto-grants-2011_05