HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 118432152, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 118431627 | HCID 118431627 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 118432152 | HCID 118432152 | 85.9% |
Reaction Steps
5-(4′-Acetyl-biphenyl-3-yl)-1-(2-chloro-phenyl)-3-pentafluoroethyl-4,5-dihydro-1H-pyrazole (18.0 mg, 0.04 mmol) prepared in Example 107 and sodium borohydride (2.0 mg, 0.06 mmol) were added at 0° C. to methanol (2.0 mL). The reaction mixture was stirred at room temperature for 3 hours, quenched with distilled water, and then extracted with ethyl acetate three times. The combined extract was washed with brine, dried on anhydrous magnesium sulfate, and then concentrated under reduced pressure to give 17.0 mg of the titled compound as a yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09376420B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-c37e63e0c9854eabadb75c5caf0f3736 |
| Source note | uspto-grants-2016_06 |