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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642239Generated: October 29, 2026

Tetramethyltin → 1-(4-Fluoro-phenyl)-4-hydroxy-7-methyl-3-phenyl-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/642239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetramethyltinHCID 11661—
Reactant7-Chloro-1-(4-fluoro-phenyl)-4-hydroxy-3-phenyl-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid ethyl esterHCID 86617350—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-(4-Fluoro-phenyl)-4-hydroxy-7-methyl-3-phenyl-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid ethyl esterHCID 6842638852.6%

Reaction Conditions

Temperature135 °C

Reaction Steps

A mixture of 7-chloro-1-(4-fluoro-phenyl)-4-hydroxy-3-phenyl-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid ethyl ester (60 mg, 0.146 mmol), tetramethyltin (104 mg, 0.584 mmol) and Pd(PPh3)2Cl2 in DMF (1 mL) was stirred at 135° C. for 2 h; then the reaction was cooled, diluted with EtOAc, washed with water and saturated sodium chloride aqueous solution respectively, the organic phase was dried over anhydrous sodium sulfate, filtered, concentrated, the residue was purified on column to give the desired title product (30 mg); ESI MS (m/z): 391 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696223B2
Source datasetuspto-grants-2010_04
ORD IDord-5042dad116834076bff502d185ccaeaf
Source noteuspto-grants-2010_04