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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272961Generated: November 1, 2026

Sodium Bicarbonate → HCID 71765497, compound

https://huagongshe.com/reaction/2272961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
ReactantHCID 71765496HCID 71765496—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 71765497HCID 71765497—

Reaction Conditions

Temperature40 °C

Reaction Steps

Under nitrogen, a suspension of 141 mg (0.486 mmol) 3-(4-bromo-phenyl)-2H-pyrrolo[1,2-a]pyrazin-1-one, 111 mg (0.534 mmol) 1-methyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-pyrazole and 49 mg (0.58 mmol) sodium hydrogen carbonate in 1 ml DMF and 0.5 ml water is heated to 40° C. Then 6.8 mg (0.010 mmol) bis(triphenylphosphine)-palladium(II)-chloride is added. The reaction mixture is heated to 80° C. and stirred at this temperature for 20 hours. The reaction mixture is cooled to room temperature and excess water is added. The resulting precipitate is filtered off and washed with water. The residue is chromatographed on a silica gel column with methanol/dichloromethane as eluent to give 3-[4-(1-methyl-1H-pyrazol-4-yl)phenyl]-2H-pyrrolo[1,2-a]pyrazin-1-one as light yellow crystals; HPLC/MS 2.09 min (B), [M+H] 291;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120805B2
Source datasetuspto-grants-2015_09
ORD IDord-8d973d385e4644fa9eb6b3d4e9c99077
Source noteuspto-grants-2015_09