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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289948Generated: October 31, 2026

2-Methylphenyl boronic acid → HCID 178469644, compound

https://huagongshe.com/reaction/2289948

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylphenyl boronic acidHCID 2733267—
ReactantBarium hydroxide, octahydrateHCID 17749109—
ReactantHCID 178469647HCID 178469647—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178469644HCID 17846964447%

Reaction Conditions

Temperature80 °C

Reaction Steps

6-Iodo-8-fluoro-4-hydroxy-3-quinolinecarboxylic acid ethyl ester (903 mg) from Example No. 5 and o-tolueneboronic acid (374 mg) are dissolved in DMF (50 mL) and at 50° C. a solution of barium hydroxide octahydrate (1.18 g) in water (5 mL) is added followed by palladium tetrakistriphenylphosphine (58 mg). The mixture is heated at 80° C. for 20 h, allowed to cool to rt, poured into water (200 mL), and extracted with ethyl acetate (3×100 mL). The organic layer is washed with brine (25 mL), dried (MgSO4), and concentrated. The solid is then triturated with MTBE, and filtered to afford 382 mg of 6-(2-methylphenyl)-8-fluoro-4-hydroxy-3-quinoline-carboxylic acid ethyl ester. The crude ester is mixed with 4-chlorobenzylamine (380 mg) and is heated to 190° C. for 1 h. The mixture is diluted with toluene (4 mL), allowed to cool to rt, poured into a mixture of 50% acetic acid (10 mL) and 1 N hydrochloric acid (25 mL), and is extracted with ethyl acetate (3×25 mL). The organic layer is dried (MgSO4) and allowed to crystallize. Recrystallization from acetic acid/water affords 166 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093732
Source datasetuspto-grants-2000_07
ORD IDord-64bbc90262374e5d9c4f86f89c70d0ca
Source noteuspto-grants-2000_07