HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705041Generated: October 30, 2026
Dimethylformamide → HCID 69091337, compound
https://huagongshe.com/reaction/705041
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Methyl 6-bromopyridine-2-carboxylate | HCID 16217886 | — |
| Reactant | HCID 178505992 | HCID 178505992 | — |
| Catalyst | Copper oxide | HCID 14829 | — |
| Catalyst | Ferric acetylacetonate | HCID 5483663 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 69091337 | HCID 69091337 | — |
Reaction Steps
30 ml of DMF were added to 1.88 g (11.5 mmol) of 3-(5-fluoro-3-pyridinyl)-1H-pyrazole (preparation cf. step 2), 2.50 g (11.5 mmol) of methyl 6-bromo-2-pyridinecarboxylate, 92.0 mg (1.15 mmol) of copper (II) oxide, 7.54 g (23.10 mmol) of cesium carbonate and 1.22 g (3.47 mmol) of iron(III) acetylacetonate, and the mixture was stirred at 90° C. for 60 hours. The entire reaction mixture was then cooled to room temperature, and water was added. The reaction mixture was then extracted with ethyl acetate. The organic phase was separated off, dried, filtered and concentrated under reduced pressure. The residue was purified by chromatography on silica gel. This gave 191 mg (5.0% of theory) of methyl 6-[3-(5-fluoro-3-pyridinyl)-1H-pyrazol-1-yl]-2-pyridinecarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09173396B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-51486ae8918c4204a8b3eccbcd06da05 |
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| Source note | uspto-grants-2015_11 |
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