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 | HCID 86761232 | HCID 86761232 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 68775704 | HCID 68775704 | 57.6% |
Reaction Steps
A mixture of 2,2,2-trifluoroethyl [6-(acetylamino)pyridin-3-yl]carbamate (274 mg, 0.839 mmol), 4-[4-(4-fluorophenyl)-1,3-thiazol-2-yl]piperidine (200 mg, 0.762 mmol) and diisopropylethylamine (0.266 ml, 1.52 mmol) in dimethylsulfoxide (2.5 ml) was stirred at 70° C. for 12 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 recrystallized from a mixed solvent of hexane and tetrahydrofuran to give the desired product (193 mg, 57.6%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07851473B2 |
|---|
| Source dataset | uspto-grants-2010_12 |
|---|
| ORD ID | ord-d0809ead93774d19a91d81c85a8ba7b7 |
|---|
| Source note | uspto-grants-2010_12 |
|---|