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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593004Generated: October 26, 2026

Acetyl chloride → 4-{3-[4-(Methylthio)benzyl]-1,2,4-oxadiazol-5-yl}piperidine hydrochloride

https://huagongshe.com/reaction/1593004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTert-butyl 4-{3-[4-(methylthio)benzyl]-1,2,4-oxadiazol-5-yl}piperidine-1-carboxylateHCID 68710908—
SolventMethanolHCID 887—
Product4-{3-[4-(Methylthio)benzyl]-1,2,4-oxadiazol-5-yl}piperidine hydrochlorideHCID 68709132100.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

Acetyl chloride (86 μL, 1.21 mmol) was added dropwise to methanol (0.5 mL) and stirred for 10 minutes then added to tert-butyl 4-{3-[4-(methylthio)benzyl]-1,2,4-oxadiazol-5-yl}piperidine-1-carboxylate (237 mg, 0.61 mmol) in MeOH (5 mL) and the mixture heated to 60° C. for 1 hour and the solvents evaporated to give a the title compound as a yellow powder, (199 mg, 100%); MS: 290 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07294636B2
Source datasetuspto-grants-2007_11
ORD IDord-360ff4f085184d7db5c58602999b9d03
Source noteuspto-grants-2007_11