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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425953Generated: October 29, 2026

1-(5-(4-Bromophenyl)-4-hydroxythiophen-3-YL)ethan-1-one → HCID 73224892, compound

https://huagongshe.com/reaction/2425953

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(5-(4-Bromophenyl)-4-hydroxythiophen-3-YL)ethan-1-oneHCID 44207290—
ReactantHCID 57688156HCID 57688156—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 73224892HCID 7322489281%

Reaction Conditions

Temperature110 °C

Reaction Steps

2-(4-Bromophenyl)-3-hydroxy-4-methylcarbonylthiophene (50.5 mg, 0.17 mmol) (synthesized in accordance with WO2004/108683) and 5-hydrazinocarbonylthiophene-2-carboxylic acid 3-picolylamide prepared in Reference Synthetic Example 11 were dissolved in dimethylsulfoxide (4.0 mL) and heated at 110° C. for 24 hours. The solvent was evaporated, and the residue was washed with methanol and water to give the desired product (yield 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968542B2
Source datasetuspto-grants-2011_06
ORD IDord-0b8eed29b5344a2e9b6bdad4004eeeae
Source noteuspto-grants-2011_06