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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915547Generated: October 31, 2026

Sodium Carbonate → 4-(6-Phenylpyrazolo[1,5-a]pyrimidin-5-yl)benzaldehyde

https://huagongshe.com/reaction/1915547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Formylphenylboronic AcidHCID 591073—
Reactant5-Chloro-6-phenylpyrazolo[1,5-a]pyrimidineHCID 86630664—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-(6-Phenylpyrazolo[1,5-a]pyrimidin-5-yl)benzaldehydeHCID 86630665—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 300 mg of the mixture from step 3 and 360 mg 4-formylphenylboronic acid in 9 ml 1,2-dimethoxyethane are added 1.8 ml of a 10% w/w sodium carbonate solution and 36 mg dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium (II) and the resulting mixture is heated to 80° C. under an inert gas atmosphere for 18 h. The work up is performed by diluting the reaction mixture with water and dichloromethane, separating the phases and extraction of the aqueous phase with dichloromethane. The combined organic layers are dried over sodium sulphate, evaporated and the residue is purified by chromatography on silica gel (dichloromethane/methanol). The product is crystallized from ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614218B2
Source datasetuspto-grants-2013_12
ORD IDord-17635809b8bc4096ae7352b19f11f84a
Source noteuspto-grants-2013_12