HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 10501216, compound → HCID 19607806, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 10501216 | HCID 10501216 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19607806 | HCID 19607806 | 79.9% |
Reaction Steps
Ethanol (50 ml) is added to 10% Pd--C (0.1 g) and thereto is added-1-[4-(3-nitrobenzoylamino)benzoyl]-1,2,3,4-tetrahydroquinoline (0.73 g). The mixture is subjected to catalytic reduction at ordinary temperature under atmospheric pressure of hydrogen. After completion of the reduction, 10% Pd--C is removed by filtration and the filtrate is concentrated under reduced pressure. The residue is extracted with dichloromethane and the extract is dried over magnesium sulfate. The solvent is distilled off under reduced pressure and recrystallized from methanol to give 1-[4-(3-aminobenzoylamino)benzoyl]-1,2,3,4-tetrahydroquinoline (0.54 g) as white powder, m.p. 205.5°-206.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753677 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-298d5a8a480d42708f106122a7f7947d |
| Source note | uspto-grants-1998_05 |