HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263220Generated: October 26, 2026
Water → 4-[4-(4-fluorophenyl)-1,3-thiazol-2-yl]-N-pyridazin-3-ylpiperidine-1-carboxamide
https://huagongshe.com/reaction/2263220
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-[4-(4-Fluorophenyl)-1,3-thiazol-2-yl]piperidine | HCID 24261841 | — |
| Reactant | 2,2,2-Trichloroethyl pyridazin-3-ylcarbamate | HCID 68576698 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-[4-(4-fluorophenyl)-1,3-thiazol-2-yl]-N-pyridazin-3-ylpiperidine-1-carboxamide | HCID 68777881 | 58% |
Reaction Steps
A mixture of 2,2,2-trichloroethyl pyridazin-3-ylcarbamate (170 mg, 0.629 mmol), 4-[4-(4-fluorophenyl)-1,3-thiazol-2-yl]piperidine (150 mg, 0.572 mmol) and diisopropylethylamine (0.199 ml, 1.14 mmol) in dimethylsulfoxide (2.0 ml) was stirred at 70° C. for 6 hours. Water was poured into the reaction solution, and the mixture was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate) and recrystallized from a mixed solvent of hexane and tetrahydrofuran to give the desired product (127 mg, 58.0%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07851473B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-47d2d2924df7413290605dc278750192 |
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| Source note | uspto-grants-2010_12 |
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