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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178225Generated: November 1, 2026

Boron trifluoride etherate → HCID 53443879, compound

https://huagongshe.com/reaction/2178225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
Reactant1,3,5-TriazineHCID 9262—
Reactant5-Amino-1-(4-bromophenyl)-1H-pyrazole-4-carboxylic acidHCID 4057029—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
ProductHCID 53443879HCID 53443879—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 1,3,5-triazine (0.575 g, 7.09 mmol) and 5-amino-1-(4-bromophenyl)-1H-pyrazole-4-carboxylic acid (22A) (2 g, 7.09 mmol) in DMSO (30 mL) was added boron trifluoride etherate (1.08 mL, 8.51 mmol). The resulting mixture was heated at 120° C. for 20 hours, cooled, diluted with EtOAc and washed with 1% NaOH and brine. The organic layer was dried over Na2SO4 and concentrated under reduced pressure. The residue was triturated with small amount of EtOAc and the precipitate was collected to provide the desired product 1-(4-bromophenyl)-1H-pyrazolo[3,4-d]pyrimidine (22B): 1H NMR (400 MHz, DMSO-D6) δ ppm 9.47 (1H, s), 9.16 (1H, s), 8.68 (1H, s), 8.22 (2H, d), 7.80 (2H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067928B2
Source datasetuspto-grants-2015_06
ORD IDord-7a408d19a15e4bbb9ebab6097fb3cb9e
Source noteuspto-grants-2015_06