HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → HCID 178522800, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | N-benzhydryl-2-(benzyloxymethyl)-4-hydroxypyrimidine-5-carboxamide | HCID 178522799 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178522800 | HCID 178522800 | 21% |
Reaction Steps
A mixture of step E product, 2-f, (3.0 g, 7 mmol), ammonium formate (0.9 g, 14 mmol) and Pd/C (0.6 g) in MeOH (70 mL) was refluxed overnight. The reaction solution was filtered. The filtrate was evaporated under vacuum to obtain a residue, which was purified by silica gel chromatography by eluting with PE:EA=1:2 and DCM:MeOH=10:1 to afford the product, 2-g, (0.51 g, 21%). 1H NMR (300 MHz, CDCl3): δ4.47 (s, 2H), 6.30-6.32 (d, Hz, 1H), 7.23-7.25 (m, 11H), 8.72 (s, 1H), 9.98-10.00 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09034851B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-3870b3f3c2ed49b68341be4b9c563be1 |
| Source note | uspto-grants-2015_05 |