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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119399Generated: October 30, 2026

2,5-Dichlorobenzooxazole → benzyl(2S)-1-(5-chloro-1,3-benzoxazol-2-yl)-2-piperidinecarboxylate

https://huagongshe.com/reaction/2119399

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DichlorobenzooxazoleHCID 10397578—
Reactant(2S)-2-((benzyloxy)carbonyl]piperidinium chlorideHCID 86591486—
Productbenzyl(2S)-1-(5-chloro-1,3-benzoxazol-2-yl)-2-piperidinecarboxylateHCID 53932308—

Reaction Steps

The title compound was prepared by a similar method to Preparation 2 from (2S)-2-[(benzyloxy)carbonyl]piperidinium chloride [see EP 530167 A1 930303] and 2,5-dichloro-1,3-benzoxazole [see J.O.C. (1996), 61(10), 3289-3297]. The crude product was purified by column chromatography on silica gel eluting with a solvent system of 95:5, by volume, hexane:ethyl acetate to afford benzyl (2S)-1-(5-chloro-1,3-benzoxazol-2-yl)-2-piperidinecarboxylate as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06686357B1
Source datasetuspto-grants-2004_02
ORD IDord-37a51b6a33434ad8aafa3676e7dfb32a
Source noteuspto-grants-2004_02