HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → HCID 68183055, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 8-Nitro-7-quinolinecarboxaldehyde | HCID 11769554 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68183055 | HCID 68183055 | 71.6% |
Reaction Steps
A solution of 8-nitro-quinoline-7-carbaldehyde (Intermediate 204) (500 mg, 2.4 mmol) and aniline (270 μl, 2.9 mmol) in MeOH (20 ml) under a nitrogen atmosphere was stirred at room temperature for 16 hours. Sodium borohydride (269 mg, 7.1 mmol) was added and stirring continued at room temperature for 1 h. The reaction mixture was concentrated in vacuo and residue was diluted with sat. NaHCO3 solution (30 ml) and was extracted with DCM. The organic phases were dried (MgSO4) and concentrated in vacuo. The crude residue was purified by column chromatography with heptane/EtOAc gradient elution to give the title compound (0.48 g, 69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09102688B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-9944d5d4a6124901bbc54a3baa828a32 |
| Source note | uspto-grants-2015_08 |