HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570105Generated: October 30, 2026
Methanol → 1-Methoxy-4-methylamino-piperidine-4-carboxylic acid methyl ester
https://huagongshe.com/reaction/570105
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-Methoxy-4-methylamino-piperidine-4-carboxylic acid | HCID 58537906 | — |
| Product | 1-Methoxy-4-methylamino-piperidine-4-carboxylic acid methyl ester | HCID 58537903 | — |
Reaction Steps
To a suspension of 1-methoxy-4-methylamino-piperidine-4-carboxylic acid (2.0 g, 10.63 mmol) in methanol (50 ml) at 0-10° C. was added thionyl chloride (2.29 ml, 3.76 g, 31.57 mmol) and the reaction mixture was heated at reflux overnight. After cooling, the mixture was concentrated, the residue diluted with ice water (20 ml) and neutralised with aqueous sodium bicarbonate. The aqueous phase was extracted with ethyl acetate (4×25 ml) and dichloromethane (4×50 ml), the combined organic layers washed with aqueous sodium bicarbonate (15 ml) and brine (15 ml), dried over sodium sulfate and concentrated. Yield: 0.76 g of 1-methoxy-4-methylamino-piperidine-4-carboxylic acid methyl ester (compound P5.4) as a viscous, orange oil. The spectral data of this crude material were identical to those described above under preparation example 6, step 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09023760B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-9c3617cb09e54e2b90b54d0e61c8f534 |
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| Source note | uspto-grants-2015_05 |
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