HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178522995, compound → 5-benzyloxy-N-(4-fluoro-benzyl)-6-formyl-4-hydroxy-nicotinic acid amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178522995 | HCID 178522995 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-benzyloxy-N-(4-fluoro-benzyl)-6-formyl-4-hydroxy-nicotinic acid amide | HCID 178519984 | 84.2% |
Reaction Steps
After manganese dioxide (49 g) was added to a suspension of the compound 10 (9.8 g, 25.6 mmol) in chloroform (490 ml), the mixture was stirred at room temperature for 1 hour. After the reaction solution was stirred at 60° C. for 20 minutes, Celite filtration was performed, and this was washed with chloroform heated at 50° C. The filtrate was distilled off under reduced pressure to obtain 5-benzyloxy-N-(4-fluoro-benzyl)-6-formyl-4-hydroxy-nicotinic acid amide 12 (8.2 g, 84%) as a pale yellow crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08188271B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-7ac07432362e4677b2dda02dd377996b |
| Source note | uspto-grants-2012_05 |