HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 67183816, compound → 1-[3-(1-Piperidin-4-yl-4-pyridin-4-yl-1h-pyrazol-3-yl)-phenyl]-3-(4-trifluoromethyl-phenyl)-urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 67183816 | HCID 67183816 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-[3-(1-Piperidin-4-yl-4-pyridin-4-yl-1h-pyrazol-3-yl)-phenyl]-3-(4-trifluoromethyl-phenyl)-urea | HCID 44622813 | — |
Reaction Steps
To 4-(4-pyridin-4-yl-3-{3-[3-(4-trifluoromethyl-phenyl)-ureido]-phenyl}-pyrazol-1-yl)-piperidine-1-carboxylic acid tert-butyl ester (100 mg, 0.16 mmol) in dioxane (2 mL) HCl 4M in dioxane (1 mL, 3.30 mmol) was added. After one hour the reaction was diluted with ethyl acetate (50 mL) and washed with saturated NaHCO3 solution (3×50 mL) and brine (1×50 mL). The organic phase was dried over Na2SO4, filtered and the solvent was evaporated under reduced pressure. The deprotected urea was isolated by reverse phase chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541575B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-12dbcc4149eb4bd581d12cb21bb2d37c |
| Source note | uspto-grants-2013_09 |