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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506002Generated: October 29, 2026

Sulfuric Acid → 3-(3-Trifluoromethylphenyl)-9H-dipyrido[2,3-b;4',3'-d]pyrrole-6-carboxylic acid

https://huagongshe.com/reaction/1506002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant3-(Trifluoromethyl)phenylboronic acidHCID 2734388—
Reactant3-bromo-9H-dipyrido[2,3-b;4',3'-d]pyrrole-6-carboxylic acidHCID 67027538—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
SolventSodium CarbonateHCID 10340—
Product3-(3-Trifluoromethylphenyl)-9H-dipyrido[2,3-b;4',3'-d]pyrrole-6-carboxylic acidHCID 58266714—

Reaction Conditions

Temperature140 °C

Reaction Steps

A degassed mixture of 3-bromo-9H-dipyrido[2,3-b;4′,3′-d]pyrrole-6-carboxylic acid (20.0 mg, 68.5 μmol), 3-(trifluoromethyl)phenylboronic acid (19.5 mg, 0.103 mmol), and bis(triphenylphosphine)palladium(II) dichloride (2.4 mg, 3.4 μmol) in acetonitrile (0.3 mL) and 2N aqueous sodium carbonate solution (0.3 mL) was heated under microwave irradiation at 140° C. for 10 minutes. The cooled reaction mixture was acidified with 10% aqueous sulfuric acid. The solid was removed by filtration and the resultant filtrate was purified by preparative HPLC (5-45% MeCN over 45 min, 35 mL/min) to afford the title compound. 1H NMR (DMSO-D6, 400 MHz): 12.75 (s, 1H), 9.38-9.00 (m, 311), 8.21 (m, 1H), 7.78 (m, 2H), 7.65-7.60 (m, 2H). LCMS (Method D): RT=10.76 min, M+H+=358.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216980B2
Source datasetuspto-grants-2015_12
ORD IDord-60ebae9b5e804425ab48a27a087e3f31
Source noteuspto-grants-2015_12