HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 18433622, compound → HCID 18433566, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 18433622 | HCID 18433622 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18433566 | HCID 18433566 | — |
Reaction Steps
3-(tert-Butyldimethylsilyloxy)-5-nitroquinoline, as described above in Step E, (4.58 g, 15.04 mmol) was dissolved in EtOH (150 mL) and EtOAc (150 mL), the vessel was degassed, Pd/C (0.458 g, 10 wt %) was added and the mixture was subjected to H2 (1 atm) with vigorous stirring for 1 hour. The mixture was filtered through a celite pad and concentrated in vacuo. The residue was chromatographed on silica gel, eluting with a gradient of 0% to 10% EtOAc in CH2Cl2, to yield the above-titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06441017B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-0a867fc34bf94d41b629140b36e30aee |
| Source note | uspto-grants-2002_08 |