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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628463Generated: October 26, 2026

Sodium Carbonate → HCID 89488463, compound

https://huagongshe.com/reaction/628463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactanttert-butyl N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)carbamateHCID 49760449—
ReactantHCID 89488335HCID 89488335—
CatalystBis(tricyclohexylphosphine)palladium(II) DichlorideHCID 11556747—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 89488463HCID 89488463—

Reaction Conditions

Temperature150 °C

Reaction Steps

3-bromo-2-(4-fluorophenyl)-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole (700 mg, 2.5 mmol) and tert-butyl [4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]carbamate (727 mg, 2.27 mmol, 1.1 eq) are dissolved in 10 mL 1,4-dioxan. To this mixture is added Bis(tricyclohexylphosphine)palladium(II)-dichloride (168 mg, 0.22 mmol, 0.1 eq) and 5.4 mL sodium carbonate solution (2 molar). The reaction mixture is flushed with argon for 5 mins and then sealed. Next the mixture is heated for 12 mins at 150° C. in the microwave (Biotage). After cooling, insoluble components are filtered off over Celite and the residue washed with 1,4-dioxan. The organic phase is evaporated and the crude product purified by column chromatography over silica gel using dichloromethane/methanol (95:5) as eluent. After evaporation of the solvents 530 mg (72%) of 4-[2-(4-fluorophenyl)-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl]pyridin-2-amine are obtained as a colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09314026B2
Source datasetuspto-grants-2016_04
ORD IDord-fa4d73ebf42146b6b4ee92679d21e6c9
Source noteuspto-grants-2016_04