HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359923Generated: November 1, 2026
3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)pyridine → HCID 66633797, compound
https://huagongshe.com/reaction/2359923
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)pyridine | HCID 57416218 | — |
| Reactant | HCID 66633262 | HCID 66633262 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | HCID 66633797 | HCID 66633797 | — |
Reaction Steps
Under argon, 3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]pyridine (0.1 g, 0.37 mmol), 2-bromo-N-(methylsulphonyl)-1,3-thiazole-4-carboxamide (0.105 g, 0.37 mmol) and tetrakis(triphenylphosphine)palladium (0.013 g, 0.011 mmol) were added to a mixture, degassed by means of argon, of sodium carbonate solution in water (1.5 ml, 2 M/L) and acetonitrile (3.8 ml). The reaction mixture was stirred at 70° C. for 16 h. After cooling, the reaction mixture was poured onto water and extracted with dichloromethane. The organic phase was dried over sodium sulphate and the solvent was removed under reduced pressure. The residue was 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-3b9ffcbbdc784a1c8b65f52c1baeadc4 |
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| Source note | uspto-grants-2014_04 |
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