HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406593Generated: October 31, 2026
Sodium borohydride → HCID 86686304, compound
https://huagongshe.com/reaction/406593
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 66613393 | HCID 66613393 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86686304 | HCID 86686304 | — |
Reaction Steps
To a mixture of (2,4-difluorophenyl)-[5-(2,4-difluorophenyl)-1,3-dimethyl-1H-pyrazol-4-yl]methanone (i.e. the product of Example 7) (80 mg, 0.23 mmol) in ethanol (3 mL) at about 0° C. was added sodium borohydride (38 mg, 0.92 mmol). The reaction mixture was stirred at room temperature for 2 h, and then diluted with ice/hydrochloric acid (about 1 mL). The resulting mixture was poured onto a solid phase extraction tube (Varian Chem Elute®, prepacked with diatomaceous earth) eluting with ethyl acetate (75 mL). The ethyl acetate eluant was concentrated under reduced pressure and the resulting material was purified by MPLC (20 to 70% gradient of ethyl acetate in hexanes as eluant) to provide the title compound, a compound of the present invention, as a solid (63 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754115B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-d933960d14f04ba68ea0c35f58c5a611 |
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| Source note | uspto-grants-2014_06 |
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