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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34116Generated: October 30, 2026

Triethylamine → 3-[(E)-2-(4-fluorophenyl)ethenyl]-4-methoxy-N-(2-oxopropyl)-1H-indazole-5-carboxamide

https://huagongshe.com/reaction/34116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 86600700HCID 86600700—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3-[(E)-2-(4-fluorophenyl)ethenyl]-4-methoxy-N-(2-oxopropyl)-1H-indazole-5-carboxamideHCID 6003482880.4%

Reaction Conditions

Temperature40 °C

Reaction Steps

100 mg of 3-[(E)-2-(4-fluorophenyl)-vinyl]-4-methoxy-1H-indazole-5-carboxylic acid (2-hydroxylpropyl) amide obtained by Example 825 and 300 μl of triethylamine were dissolved in a mixed solvent of 4 mL dichloromethane/1 mL dimethyl sulfoxide, added with 1 mL of a solution of 260 mg of pyridine sulfur trioxide complex in dimethyl sulfoxide under ice cooling, and the reaction solution was heated at 40° C. for 3 hours. The reaction solution was diluted with water, extracted with ethyl acetate, washed with water, and then dried over magnesium sulfate. The solvent was evaporated, and the residue was purified by silica gel column chromatography (ethyl acetate:methanol=100:3), and then crystallized from ethyl acetate and diisopropyl ether, to afford 80 mg of the title compound as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429609B2
Source datasetuspto-grants-2008_09
ORD IDord-c21a91ae1afa4b6a9e46ab04588e2554
Source noteuspto-grants-2008_09