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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Tert-butyl 4-{3-[4-(methylthio)benzyl]-1,2,4-oxadiazol-5-yl}piperidine-1-carboxylate | HCID 68710908 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-{3-[4-(Methylthio)benzyl]-1,2,4-oxadiazol-5-yl}piperidine hydrochloride | HCID 68709132 | 100.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07294636B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-360ff4f085184d7db5c58602999b9d03 |
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| Source note | uspto-grants-2007_11 |
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