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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383700Generated: October 25, 2026

Triethylamine → HCID 59635506, compound

https://huagongshe.com/reaction/383700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-Boronothiophene-2-carboxylic acidHCID 2779807—
Reactant5-Chloropyrazolo(1,5-a)pyrimidine-3-carbaldehydeHCID 58196401—
SolventDimethylformamideHCID 6228—
ProductHCID 59635506HCID 5963550622%

Reaction Conditions

Temperature100 °C

Reaction Steps

To 5-chloropyrazolo[1,5-a]pyrimidine-3-carbaldehyde (590 mg, 3.25 mmol) in DMF was added 5-Carboxythiophene-2-boronic acid (670 mg, 3.9 mmol), triethylamine (1.13 mL, 8.11 mmol) and dichloro-((bis-diphenylphosphino)ferrocenyl)palladium(II) dichloromethane adduct (120 mg, 0.16 mmol). The reaction mixture was degassed with nitrogen then heated at 100° C. for 2 hours. The mixture was cooled to room temperature, diluted with 1N HCl, and filtered. The collected solid was washed with 1N HCl and dried under vacuum. The desired product, 5-(3-formylpyrazolo[1,5-a]pyrimidin-5-yl)thiophene-2-carboxylic acid, was recovered in 22% yield and used for the next step without further purification. LCMS (M+1=274)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367681B2
Source datasetuspto-grants-2013_02
ORD IDord-c458f6ad621e4135b78eb5bc1a785b9a
Source noteuspto-grants-2013_02