HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[5-(benzyloxy)pyrimidin-2-yl]hexanamide → N-(5-Hydroxypyrimidin-2-YL)hexanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[5-(benzyloxy)pyrimidin-2-yl]hexanamide | HCID 67391208 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(5-Hydroxypyrimidin-2-YL)hexanamide | HCID 58339660 | 46,142.898% |
Reaction Steps
N-[5-(Benzyloxy)pyrimidin-2-yl]hexanamide (87.1 g, 0.29 mmol) was dissolved in methanol (2.4 L), the solution was added with 10% palladium/carbon (20 g), and the mixture was stirred at room temperature for 3 hours under hydrogen atmosphere. The reaction mixture was filtered, the filtrate was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (chloroform:methanol=30:1) to obtain N-(5-hydroxypyrimidin-2-yl)hexanamide (28.0 g, 46%) as pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08012989B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-2cc988c048fc44649cb21d015dd6667d |
| Source note | uspto-grants-2011_09 |