HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 4-{2-[(Piperidin-4-yl)oxy]pyrimidin-5-yl}benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 23115990 | HCID 23115990 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-{2-[(Piperidin-4-yl)oxy]pyrimidin-5-yl}benzonitrile | HCID 23115971 | 100.3% |
Reaction Steps
Trifluoroacetic acid (1.5 ml) was added to a methylene chloride solution (2.0 ml) of 2-(1-t-butoxycarbonylpiperidin-4-yloxy)-5-(4-cyanophenyl)pyrimidine (122 mg, 0.32 mmol) at room temperature, and stirred for 2.5 hours at the temperature. The reaction solution was concentrated under reduced pressure, and the residue was extracted with chloroform. The organic layer was washed with aqueous saturated sodium bicarbonate solution and saturated saline solution in that order, dried with anhydrous sodium sulfate, and concentrated under reduced pressure to obtain the entitled compound (90 mg, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08044070B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-c031c6a3c5e14a6a9ea1dfa87283028f |
| Source note | uspto-grants-2011_10 |