HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ceric ammonium nitrate → HCID 21919205, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ceric ammonium nitrate | HCID 180504 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 21919193 | HCID 21919193 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 21919205 | HCID 21919205 | 68% |
Reaction Steps
N-[3-(3,4,5,6-Tetramethoxy-2-methylbenzyl)-2-(3-pyridyl)benzoyl]piperidine (80 mg, 0.1632 mmol) was dissolved in a mixed solvent of acetonitrile (9 ml) and water (3 ml), then CAN (128 mg, 0.2335 mmol) was added thereto at room temperature and the mixture was stirred for 1 hour. The reaction solution poured into water, neutralized with a saturated aqueous solution of sodium hydrogen carbonate and extracted with ethyl acetate. The extract was washed with water and dried and the solvent was evaporated therefrom. The residue was purified by preparative thin layer silica gel (hexane:ethyl acetate=1:3) to give the title compound (51 mg, 0.1108 mmol, 68%). This compound was converted to a methanesulfonate by the method according to Example 58.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07122543B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-48f93f681c6d4f6ca155a329f4c721fd |
| Source note | uspto-grants-2006_10 |