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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383445Generated: October 30, 2026

Potassium Carbonate → HCID 44465600, compound

https://huagongshe.com/reaction/383445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantThiophene-3-boronic acidHCID 581760—
ReactantHCID 44241532HCID 44241532—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventEthanol tetrahydrofuran waterHCID 18504229—
ProductHCID 44465600HCID 44465600—

Reaction Conditions

Temperature100 °C

Reaction Steps

To 2-bromo-1-(4-hydroxy-phenyl)-1H-indole-3-carbonitrile (Example 1) was added 2 eq 3-thiopheneboronic acid, 2.1 eq potassium carbonate and 10 mol % tetrakis(triphenylphosphine) palladium. THF:EtOH:H2O (4:1:0.5) was added and the vial was flushed with nitrogen, sealed and stirred at 100° C. for 48 hours. The reaction mixture was cooled to rt, diluted with H2O, extracted with EtOAc and filtered through silica. The organic phase was evaporated to dryness and the crude product was subjected to reversed phase preparative HPLC. Appropriate fractions were combined, evaporated, and identified by 1H-NMR and LC/MS. Purity was determined by analytical HPLC. ES/MS m/z: 317.9 (M+H), 314.8 (M−H); 1H NMR (acetone-d6, 500 MHz): 7.73 (m, 1H), 7.62 (dd, 1H, J=1.3, 2.9 Hz), 7.54 (dd, 1H, J=2.9, 5.0 Hz), 7.37-7.30 (m, 2H), 7.26 (m, 2H), 7.18 (m, 1H), 7.15 (dd, 1H, J=1.3, 5.0 Hz) and 7.03 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367665B2
Source datasetuspto-grants-2013_02
ORD IDord-e400b5c5dc8147849453e8e1b730a4b9
Source noteuspto-grants-2013_02