HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620534Generated: October 30, 2026
Piperidinium acetate → HCID 178464089, compound
https://huagongshe.com/reaction/1620534
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidinium acetate | HCID 3014295 | — |
| Reactant | 1-[2,4-Bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde | HCID 86678663 | — |
| Reactant | HCID 178464088 | HCID 178464088 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178464089 | HCID 178464089 | 60.8% |
Reaction Steps
To a solution of 1-[2,4-bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde (1.21 g) in 2-propanol (15 mL) was added a solution of 4-({2-[2-(diethylamino)ethoxy]ethyl}amino)-1,3-thiazol-2(5H)-one (1.85 g) in 2-propanol (5 mL), and piperidinium acetate (0.52 g) was added. The reaction mixture was stirred at 60° C. overnight and 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 (NH, methanol/ethyl acetate) to give the title compound (1.26 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-a2238f892b0640ef975c8d8b476d9985 |
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| Source note | uspto-grants-2014_07 |
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