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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855943Generated: October 31, 2026

3,5-Bis-trifluoromethylphenylboronic acid → HCID 178508667, compound

https://huagongshe.com/reaction/855943

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Bis-trifluoromethylphenylboronic acidHCID 156265—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178508676HCID 178508676—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventEthanolHCID 702—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 178508667HCID 17850866753.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine (322 mg, 0.99 mmol) in ethylene glycol dimethyl ether (3.0 mL) and ethanol (3.0 mL)at 25° C. was treated with 3,5-bis(trifluoromethyl)benzene boronic acid (510 mg, 1.98 mmol), a saturated aqueous sodium bicarbonate solution (1.5 mL), and tetrakis(triphenylphosphine)-palladium (0) (115 mg, 0.1 mmol). The resulting mixture was heated to 80° C. for 18 h, cooled, filtered and the isolated solids washed with ethyl acetate. The filtrate was pre-absorbed onto silica gel and purified by flash chromatography (Merck Silica gel 60, 230-400 mesh, 90/10/1 methylene chloride/methanol/ammonium hydroxide) to give 6-(3,5-bis-trifluoromethyl-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine (218 mg, 53.5%) as a yellow solid; EI-HRMS m/e calcd for C18H11F6N5 (M+) 411.0918. Found 411.0921.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262297B2
Source datasetuspto-grants-2007_08
ORD IDord-16ef8f855ad04555aa1b5d4386b21960
Source noteuspto-grants-2007_08