HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphorus oxychloride → 8-bromo-2-chloro-4-nitro-10H-chromeno[3,2-b]pyridin-10-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 8-bromo-4-nitro-10-oxo-10H-chromeno[3,2-b]pyridine 1-oxide | HCID 67382950 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8-bromo-2-chloro-4-nitro-10H-chromeno[3,2-b]pyridin-10-one | HCID 86658470 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A suspension of 8-bromo-4-nitro-10-oxo-10H-chromeno[3,2-b]pyridine 1-oxide (90 mg, 0.267 mmol) in 1 mL of dry DMF was added dropwise to a solution of phosphorus oxychloride (44.0 μL, 0.481 mmol) in 0.2 mL of DMF and 0.5 mL of toluene at 0° C. After stirring at 0° C. for 0.5 h, the reaction was quenched with saturated NaHCO3 and extracted with ethyl acetate (5×5 mL). The combined organics were dried over sodium sulfate, filtered and evaporated to dryness. Purification of the crude residue by column chromatography (CH2Cl2 to CH2Cl2/EA=100:3) gave 8-bromo-2-chloro-4-nitro-10H-chromeno[3,2-b]pyridin-10-one as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08883782B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-a82393c7c51745938b7ea0caf5f0bd70 |
| Source note | uspto-grants-2014_11 |