HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620498Generated: October 25, 2026
tert-Butyl 4-formylpiperidine-1-carboxylate → HCID 178456946, compound
https://huagongshe.com/reaction/1620498
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl 4-formylpiperidine-1-carboxylate | HCID 1514430 | — |
| Reactant | Piperidinium acetate | HCID 3014295 | — |
| Reactant | HCID 178456890 | HCID 178456890 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178456946 | HCID 178456946 | 76.3% |
Reaction Steps
To a solution of tert-butyl 4-formylpiperidine-1-carboxylate (11.2 g) in 2-propanol (230 mL) were added 4-(prop-2-yn-1-ylamino)-1,3-thiazol-2(5H)-one (16.3 g) and piperidinium acetate (3.90 g). The reaction mixture was stirred at 60° C. overnight, and the solvent was evaporated under reduced pressure. Ethyl acetate was added to the residue, the precipitate was removed, and the filtrate was concentrated. Water was added to the residue, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (14.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772277B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-2d1f4c70c0e44e019a253e196f4f8a92 |
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| Source note | uspto-grants-2014_07 |
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