HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657657Generated: October 30, 2026
Hydrochloric Acid → HCID 69107963, compound
https://huagongshe.com/reaction/657657
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 13929038 | HCID 13929038 | — |
| Reactant | HCID 23150273 | HCID 23150273 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 69107963 | HCID 69107963 | 23.6% |
Reaction Steps
To a solution of 4-[4-(3-chloropropoxy)phenyl]pyridine 1-oxide (231 mg) and triethylamine (366 μL) in N,N-dimethylformamide (5 mL) are added potassium carbonate (363 mg) and (3S)-3-methylpiperidine mandelate (264 mg). The mixture is stirred at a temperature close to 60° C. for four hours. An additional amount of (3S)-3-methylpiperidine mandelate (100 mg) is added and heating is continued overnight. The suspension is filtered and the precipitate washed with ethyl acetate. The combined organic phases are concentrated under reduced pressure. The residue is purified twice by column chromatography over silica gel using a gradient dichloromethane/methanol/triethylamine from 100/0/0 to 95/5/0.1. Fractions containing the expected product are pooled and concentrated under reduced pressure to give 90 mg of the crude base which is converted to the hydrochloride with an ethereal solution of hydrogen chloride in ethanol to give 75 mg of (3S)-4-{4-[3-(3-methylpiperidin-1-yl)propoxy]phenyl}pyridine 1-oxide, hydrochloride melting at 74° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076329B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-2b9bce58c73449bb8f5c62a9f2b51f14 |
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| Source note | uspto-grants-2011_12 |
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