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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298867Generated: November 1, 2026

2-Chloro-5,6-dimethyl-1,3-benzoxazole → benzyl (2S)-1-[5,6-dimethyl-1,3-benzoxazol-2-yl]-2-piperidinecarboxylate

https://huagongshe.com/reaction/2298867

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5,6-dimethyl-1,3-benzoxazoleHCID 14074187—
Reactant(2S)-2-((benzyloxy)carbonyl]piperidinium chlorideHCID 86591486—
Productbenzyl (2S)-1-[5,6-dimethyl-1,3-benzoxazol-2-yl]-2-piperidinecarboxylateHCID 54542247—

Reaction Steps

The title compound was prepared by a similar method to Preparation 2 from 2-chloro-5,6-dimethyl-1,3-benzoxazole [see J.Med. Chem. (1972), 15, 523-9] and (2S)-2-[(benzyloxy)carbonyl]piperidine [see EP 530167 A1 930303]. The crude product was purified by column chromatography on silica gel eluting with a solvent gradient of 100 : 0 changing to 80:20, by volume, hexane:ethyl acetate to afford benzyl (2S)-1-[5,6-dimethyl-1,3-benzoxazol-2-yl]-2-piperidinecarboxylate as a yellow coloured solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495549B1
Source datasetuspto-grants-2002_12
ORD IDord-84520227c9074c5ca930f98c27e35a18
Source noteuspto-grants-2002_12