HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359920Generated: October 26, 2026
6-Bromopyridine-2-sulfonamide → 6-[1-(pyridin-3-yl)-1H-pyrazol-4-yl]pyridine-2-sulphonamide
https://huagongshe.com/reaction/2359920
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Bromopyridine-2-sulfonamide | HCID 57345816 | — |
| Reactant | 3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)pyridine | HCID 57416218 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | 6-[1-(pyridin-3-yl)-1H-pyrazol-4-yl]pyridine-2-sulphonamide | HCID 66633631 | — |
Reaction Steps
Under argon, 3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]pyridine (0.2 g, 0.74 mmol, prepared by the methods described in WO 2011/045224), 6-bromopyridin-2-sulphonamide (0.175 g, 0.74 mmol) and tetrakis(triphenylphosphine)palladium (0.025 g, 0.022 mmol) were added to a mixture, degassed by means of argon, of sodium carbonate solution in water (2.9 ml, 2 M/L) and acetonitrile (4 ml). The reaction mixture was stirred at 70° C. for 18 h. After cooling, the reaction mixture was poured onto water and the precipitated crystals were filtered off with suction. They were subsequently stirred with diethyl ether and filtered off with suction. This gave 0.23 g (97% of theory) of 6-[1-(pyridin-3-yl)-1H-pyrazol-4-yl]pyridine-2-sulphonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08686004B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-a29f05021e9442229f8ad18f739e5945 |
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| Source note | uspto-grants-2014_04 |
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