HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69005Generated: October 28, 2026
3-Pyridinecarboxaldehyde → HCID 67984922, compound
https://huagongshe.com/reaction/69005
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Pyridinecarboxaldehyde | HCID 10371 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 70656790 | HCID 70656790 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 67984922 | HCID 67984922 | — |
Reaction Steps
Pyridine-3-carbaldehyde (0.076 ml) was added to a 1,2-dichloroethane solution (3 ml) of 1-methyl-6-{5-[(pyridin-3-ylmethyl)-amino]-pentyloxy}-1H-quinolin-2-one (237 mg). The mixture was stirred for 30 minutes at room temperature. Sodium triacetoxyborohydride (0.23 g) was added to the mixture, and the mixture was stirred at room temperature for 3 days. A saturated sodium hydrogencarbonate aqueous solution was added to the reaction mixture, followed by extraction using dichloromethane. The organic layer was dried with anhydrous sodium sulfate, and condensed under reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate:hexane=1:1). The purified product was condensed under reduced pressure to give the title compound (247 mg) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08822453B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-194ff3f2c243413bb364fc1d148bb880 |
|---|
| Source note | uspto-grants-2014_09 |
|---|