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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841935Generated: October 26, 2026

2-Chlorobenzoxazole → methyl (2S)-1-(1,3-benzoxazol-2-yl)-2-piperidinecarboxylate

https://huagongshe.com/reaction/841935

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzoxazoleHCID 11986—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 131722236HCID 131722236—
SolventAcetonitrileHCID 6342—
Productmethyl (2S)-1-(1,3-benzoxazol-2-yl)-2-piperidinecarboxylateHCID 10220819—

Reaction Steps

Ethyldiisopropylamine (6.52 ml) was added to a solution of (2S)-2-(methoxycarbonyl)piperidinium chloride (3.057 g) [see Preparation 1] and 2-chlorobenzoxazole (2.13 ml) in acetonitrile (50 ml). The reaction mixture was stirred at room temperature for 18 hours and then at 50° C. for a further 2 hours. The solvent was removed under reduced pressure and the residue partitioned between ethyl acetate and water, the organic layer was separated, dried over magnesium sulphate and the solvent removed under reduced pressure. The crude product was purified by column chromatography on silica gel eluting with a solvent gradient of 80:10:0, changing to 0:100:0, followed by 0:95:5, by volume, hexane:ethyl acetate:methanol, to afford methyl (2S)-1-(1,3-benzoxazol-2-yl)-2-piperidinecarboxylate (3.18 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372736B1
Source datasetuspto-grants-2002_04
ORD IDord-e61dd39540eb49fdb679353cbaa41570
Source noteuspto-grants-2002_04