Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | ethyl 5-amino-1-benzyl-1H-pyrazole-4-carboxylate | HCID 785810 | — |
| Product | HCID 23023146 | HCID 23023146 | 76% |
Reaction Steps
Sodium hydride (60% dispersion in oil, 520 mg, 13 mmol) was added portionwise to a suspension of ethyl 5-amino-1-benzylpyrazole-4-carboxylate (2.2 g, 9 mmol) in anhydrous THP (30 ml) at 0° C. The mixture was allowed to warm to room temperature and stirred for 2 h then 1-fluoro-2-nitrobenzene (1.26 g, 9 mmol) was added and the resultant deep purple suspension was stirred at room temperature for 18 h. 1 M KHSO4 was added to quench the reaction and the solvent was removed in vacuo. The residue was dissolved in ethyl acetate and the solution was washed with 0.3 M KHSO4, sat. NaHCO3 and brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (eluant 75% pet. ether/25% ethyl acetate) to yield ethyl 1-benzyl-5-(2′-nitrophenylamino)pyrazole-4-carboxylate (2.5 g, 76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07407949B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-ebf52a54d1464590b7560c2a5da0b72f |
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| Source note | uspto-grants-2008_08 |
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