HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 10249539, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 10452578 | HCID 10452578 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10249539 | HCID 10249539 | — |
Reaction Steps
The title compound was prepared analogous to the methods used in Example 33 using 5-[6-(4-trifluoromethyl-phenyl)-pyrimidin-4-yloxy]-1H-quinoxalin-2-one, (Example 34(b)), (0.25 g, 0.65 mmol) and sodium borohydride (0.11 mg, 2.8 mmol, Aldrich) in EtOH (5 mL). Purification by flash chromatography (0→1.5% 2M NH3/MeOH in CH2Cl2) gave the title compound as a light-yellow powder. Mp: 305° C., MS (ESI, pos. ion) m/z: 387 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07148221B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-19df310f3b5a4e56bbc7ae5326453eb3 |
| Source note | uspto-grants-2006_12 |