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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045779Generated: October 30, 2026

1,4-Dioxane → HCID 67394324, compound

https://huagongshe.com/reaction/1045779

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant2-Thiopheneboronic acidHCID 2733960—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 58447051HCID 58447051—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
ProductHCID 67394324HCID 673943248.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

A 500 mL round bottom flask was charged with tert-butyl 4-(8-bromotetrazolo[1,5-c]pyrimidin-5-yl)piperazine-1-carboxylate (5.5 g, 14.3 mmol), thiophene-2-boronic acid (2.5 g, 21.5 mmol), tetrakis(triphenylphosphine)palladium(0) (2.0 g, 1.43 mmol), potassium tert-butoxide (2.4 g, 21.5 mmol), 1,4-dioxane (200 mL) and water (50 mL). After the air was purged by bubbling N2 into the solution, the resulting mixture was stirred at 80° C. under N2 for 10 h. Work-up: the reaction mixture was diluted with 0.1 M HCl (20 mL) and washed with EtOAc (150 mL×3). The aqueous layer was then basified with solid NaHCO3 and extracted with CH2Cl2 (150 mL×3). The combined CH2Cl2 layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 1-10% MeOH in CH2Cl2 to afford 0.70 g (12%) of the product, and 0.45 g (8.7%) of tert-butyl 4-(4-amino-5-(thiophen-2-yl)pyrimidin-2-yl)piperazine-1-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569300B2
Source datasetuspto-grants-2013_10
ORD IDord-2bb17e687a544a61807092e219128361
Source noteuspto-grants-2013_10