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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476003Generated: October 30, 2026

Sodium Carbonate → HCID 68078444, compound

https://huagongshe.com/reaction/476003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3-Pyridinylboronic acidHCID 2734378—
Reactant6-Chloro-N-[(4,6-dimethyl-2-oxo-1,2-dihydro-3-pyridinyl)methyl]-1-(1-methylethyl)-1H-pyrazolo[3,4-b]pyridine-4-carboxamideHCID 56597425—
CatalystHCID 178418476HCID 178418476—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 68078444HCID 6807844442.4%

Reaction Steps

To a 5-mL microwave vial were added 6-chloro-N-[(4,6-dimethyl-2-oxo-1,2-dihydro-3-pyridinyl)methyl]-1-(1-methylethyl)-1H-pyrazolo[3,4-b]pyridine-4-carboxamide (70 mg, 0.187 mmol), 3-pyridinylboronic acid (29.9 mg, 0.243 mmol), DMSO (1.5 mL) and sodium carbonate (0.281 mL, 0.562 mmol), and the mixture was degassed with nitrogen for 10 min. Next was added bis(triphenylphosphine)palladium(II) chloride (10.51 mg, 0.015 mmol) and the vial was sealed. The reaction mixture was irradiated (microwave) at 140° C. overnight. The reaction mixture was filtered and the residue was washed with DMSO. The crude product in DMSO was purified using reverse-phase HPLC. The TFA salt of the product was neutralized using saturated NaHCO3, filtered, washed with water and dried under high vacuum to give 33 mg (42%) of product. LCMS E-S (M+H)=417.2 1H NMR (400 MHz, DMSO-d6) δ ppm 1.56 (d, J=6.4 Hz, 6H), 2.13 (s, 3H), 2.23 (s, 3H), 4.42 (d, J=4.29 Hz, 2H), 5.26-5.43 (m, 1H), 5.91 (s, 1H), 7.62 (dd, J=7.3, 5.0 Hz, 1H), 8.26 (s, 1H), 8.43 (s, 1H), 8.64 (d, J=7.8 Hz, 1H), 8.70-8.79 (m, 1H), 8.96 (br. s., 1H), 9.46 (br. s., 1H), 11.59 (br. s., 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637509B2
Source datasetuspto-grants-2014_01
ORD IDord-ea3c02dc9c4042faa3ef3e1fcd69cd5e
Source noteuspto-grants-2014_01