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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872166Generated: November 3, 2026

Sodium Carbonate → HCID 56929145, compound

https://huagongshe.com/reaction/872166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant6-chloro-2-methyl-4-(5-methyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazin-2-ylamino)pyridazin-3(2H)-oneHCID 66634699—
ReactantHCID 86697939HCID 86697939—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 56929145HCID 5692914514%

Reaction Steps

A 250-mL single-neck round-bottomed flask equipped with a magnetic stirrer and nitrogen inlet was charged with 106e (366 mg, 0.788 mmol), 106f (194 mg, 0.656 mmol), sodium carbonate (348 mg, 3.28 mmol), DMF (2 mL), water (2 mL) and 1,4-dioxane (10 mL). After bubbling nitrogen through the resulting suspension for 30 min, tetrakis(tri-phenylphosphine)palladium(0) (152 mg, 0.131 mmol) was added. A reflux condenser was attached to the flask, and the reaction mixture was heated at reflux for 16 h. After this time, the mixture was diluted with ethyl acetate (150 mL) and water (100 mL), and the layers were separated. The aqueous layer was extracted with ethyl acetate (2×100 mL), and the combined organic layers were washed with brine (100 mL) and dried over sodium sulfate. The drying agent was removed by filtration. The filtrate was concentrated under reduced pressure, and the resulting residue was dissolved in THF (2 mL), water (2 mL) and methanol (2 mL). Lithium hydroxide monohydrate (138 mg, 3.28 mmol) was added, and the mixture was stirred at room temperature for 16 h. After this time, the mixture was diluted with ethyl acetate (150 mL) and water (100 mL), and the layers were separated. The aqueous layer was extracted with ethyl acetate (2×100 mL), and the combined organic layers were washed with brine (100 mL) and dried over sodium sulfate. The drying agent was removed by filtration. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by flash column chromatography (silica, 90:10 methylene chloride/methanol) to afford 106 in 14% yield (51 mg) as an amorphous off-white solid: mp 145-147° C.; 1H NMR (500 MHz, DMSO-d6) δ 9.20 (s, 1H), 7.89 (s, 1H), 7.55 (d, J=8.5 Hz, 1H), 7.49-7.47 (m, 2H), 7.41 (dd, J=7.0, 2.0 Hz, 1H), 6.87-6.84 (m, 2H), 5.99 (s, 1H), 4.82 (s, 2H), 4.62 (t, J=5.5 Hz, 1H), 4.40 (d, J=5.5 Hz, 2H), 3.96 (t, J=5.5 Hz, 2H), 3.75 (s, 3H), 3.52-3.50 (m, 4H), 2.98 (s, 3H), 2.79 (t, J=5.5 Hz, 2H), 2.35 (s, 3H), 1.09 (t, J=7.0 Hz, 3H); MS (ESI+) m/z 555.3 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975260B2
Source datasetuspto-grants-2015_03
ORD IDord-d1df882ebae44bbea29ef378faafbab6
Source noteuspto-grants-2015_03