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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396543Generated: November 2, 2026

Potassium Carbonate → HCID 68978422, compound

https://huagongshe.com/reaction/1396543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTriphenylphosphineHCID 11776—
Reactant1-PyrrolidineethanolHCID 76288—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
ReactantHCID 136387218HCID 136387218—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68978422HCID 68978422—

Reaction Steps

4-(6-Amino-1-methyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-2-bromo-6-fluoro-phenol hydrochloride (Example 42b) (30 mg, 0.08 mmol) is dissolved in anhydrous THF (10 ml), K2CO3 (12 mg, 0.09 mmol) is added and the reaction mixture is stirred at room temperature for 10 minutes. Triphenylphosphine (116 mg, 0.44 mmol), DIAD (0.076 ml, 0.40 mmol) and 1-(2-hydroxyethyl)pyrrolidine (0.048 ml, 0.40 mmol) are added and the reaction mixture is heated to reflux for 20 hours. After cooling to room temperature the reaction mixture is diluted with water (˜15 ml) and extracted with EtOAc (3×50 ml). The combined organic portions are dried over MgSO4, filtered and concentrated in vacuo Purification of the crude residue by flash chromatography on silica firstly eluting the non-polar impurities with iso-hexanes:EtOAc (4:1 to 1:4) then eluting the product with EtOAc:MeOH:Et3N (4:1:0.01) affords the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901134B2
Source datasetuspto-grants-2014_12
ORD IDord-945b8515043f40bd8f324a049460e75e
Source noteuspto-grants-2014_12