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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246260Generated: October 25, 2026

Dimethylformamide → 2-(6-fluoro-1H-indazol-3-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid (1-pyridin-4-yl-ethyl)-amide

https://huagongshe.com/reaction/246260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2-bromo-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid (1-pyridin-4-yl-ethyl)-amideHCID 86677968—
Reactant6-fluoro-3-(tributylstannyl)-1H-indazoleHCID 178448232—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventDiethyl EtherHCID 3283—
Product2-(6-fluoro-1H-indazol-3-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid (1-pyridin-4-yl-ethyl)-amideHCID 7128610487.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

6-Fluoro-3-tributylstannyl-1H-indazole (0.48 g, 1.13 mmol), copper(I) iodide (16 mg, 0.084 mmol) and 2-bromo-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid (1-pyridin-4-yl-ethyl)-amide (400 mg, 0.84 mmol) were combined with DMF (6 mL) to give a yellow solution. The mixture was degassed for 10 min then tetrakis(triphenylphosphine)palladium (0) (45 mg, 0.039 mmol) was added. The reaction mixture was stirred under nitrogen at 90° C. for 15 h. The reaction mixture was cooled, diluted with ether (60 mL) and washed with water and brine. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was purified by silica gel chromatography (0-3% methanol in dichloromethane with 0.5% ammonium hydroxide) to afford 390 mg (87%) of 2-(6-fluoro-1H-indazol-3-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid (1-pyridin-4-yl-ethyl)-amide as a yellow solid. MS: (M+H)+=532.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-f2da158c7d9c43afabc20f0e362bbe86
Source noteuspto-grants-2014_02