HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Nitro-7-(5-methyl-2-phenyl-4-oxazolylmethoxy)quinoline → 3-Amino-7-(5-methyl-2-phenyl-4-oxazolylmethoxy)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Nitro-7-(5-methyl-2-phenyl-4-oxazolylmethoxy)quinoline | HCID 21469326 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Amino-7-(5-methyl-2-phenyl-4-oxazolylmethoxy)quinoline | HCID 21469270 | 42% |
Reaction Steps
In a mixture of ethanol (20 mL) and ethyl acetate (10 mL) was suspended 3-nitro-7-(5-methyl-2-phenyl-4-oxazolylmethoxy)quinoline (740 mg, 2.1 mmol.), and to the suspension was added 10% palladium/carbon (50 mg). Then, catalytic reduction was performed overnight. After the completion of reaction was confirmed, the reaction mixture was filtered over Celite®, and the filtrate was placed under reduced pressure to remove the solvent. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/7 to ethyl acetate), to give 280 mg of the desired compound as brown oil (yield 42%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05693651 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-35bc5fa6f6db4664859e78d18e822f26 |
| Source note | uspto-grants-1997_12 |