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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115758Generated: October 29, 2026

2-Thiophenecarboxylic acid → HCID 11178973, compound

https://huagongshe.com/reaction/2115758

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenecarboxylic acidHCID 10700—
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBOPHCID 2724699—
ReactantHCID 67520359HCID 67520359—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 11178973HCID 11178973—

Reaction Steps

To a solution of 6-(6,7-dimethoxy-4-quinolyloxy)-5-fluoro-2-naphthylamine 2HCl (Step c, 200 mg, 0.46 mmol), thiophene-2-carboxylic acid (120 mg, 0.91 mmol, Aldrich) and DIEA (353 mg, 2.74 mmol, Aldrich) in dry DMF was added PyBOP (476 mg, 0.91 mmol, Fluka) at RT. The reaction was stirred for 16 h. It was diluted with 40 mL of EtOAc and washed with saturated aqueous NaHCO3, followed by brine. The organic phase was dried over Na2SO4 and concentrated in vacuo. The residue was purified by silica gel column chromatography (EtOAc) to give the title compound as a yellow solid. MS (ESI, pos. ion) m/z: 475.0 (M+1). Mass Calc'd for C26H19FN2O4S: 474.10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435823B2
Source datasetuspto-grants-2008_10
ORD IDord-05504a7855114264a3d3a3a9834a920d
Source noteuspto-grants-2008_10