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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692760Generated: November 2, 2026

Ethanol → HCID 57685399, compound

https://huagongshe.com/reaction/1692760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazoleHCID 45480186—
Reactant5-Chloro-7-morpholinothiazolo[4,5-d]pyrimidine-2-carbaldehydeHCID 57685392—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 57685399HCID 57685399—

Reaction Steps

A mixture of 5-chloro-7-morpholinothiazolo[4,5-d]pyrimidine-2-carbaldehyde 43, 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-indazole 1 and sodium carbonate were suspended in toluene, ethanol and water. To this was added bis(triphenylphosphine)palladium(II) chloride and the reaction vessel was flushed with argon. The reaction mixture was microwaved at 120° C. for 1 h and then partitioned between DCM and water. The organic layer was washed with brine, dried over magnesium sulfate, filtered and evaporated in vacuo. The resulting residue was purified using flash chromatography to yield 5-(1H-indazol-4-yl)-7-morpholinothiazolo[4,5-d]pyrimidine-2-carbaldehyde 55.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158626B2
Source datasetuspto-grants-2012_04
ORD IDord-d614fd8935c04503bd3e279063fab720
Source noteuspto-grants-2012_04