HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215766Generated: October 30, 2026
HCID 66933595, compound → HCID 59541743, compound
https://huagongshe.com/reaction/215766
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 66933595 | HCID 66933595 | — |
| Reactant | HCID 178418676 | HCID 178418676 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 59541743 | HCID 59541743 | — |
Reaction Steps
To a solution of 1-(4-{3-[(2R)-2-methylpyrrolidin-1-yl]propoxy}phenyl)-1H-pyrazole-4-carboxylic acid methoxymethylamide obtained in Example 23-(1) (0.25 g) in tetrahydrofuran (3 mL), a solution of 4-fluorophenylmagnesium bromide in tetrahydrofuran (1.0 M, 4.0 mL) was added dropwise in an ice bath and stirred at room temperature for 2 hours. The reaction mixture was diluted with saturated aqueous ammonium chloride and extracted with chloroform. The organic layer was dried over sodium sulfate and concentrated under reduced pressure, and the resulting residue was purified by NH-type silica gel column chromatography (eluting solvent: hexane:ethyl acetate=5:1 to 4:1) and silica gel column chromatography (eluting solvent: chloroform:methanol=95:5) to give the titled compound (0.11 g) as a light-blue solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193176B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-d7cc6eff350841e28d135cce08d03642 |
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| Source note | uspto-grants-2012_06 |
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