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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352960Generated: November 2, 2026

Thionyl Chloride → HCID 86610461, compound

https://huagongshe.com/reaction/2352960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant1-Ethyl-5-methyl-1H-pyrazole-4-carboxylic acidHCID 1075882—
Reactant6-(3-Amino-benzoyl)-1,3-dihydro-indol-2-oneHCID 59256478—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86610461HCID 8661046159.2%

Reaction Conditions

Temperature79 °C

Reaction Steps

A dry flask was charged with 1-Ethyl-5-methyl-1H-pyrazole-4-carboxylic acid (0.159 g, 1.03 mmol) and thionyl chloride (5 mL) and allowed to stir at 79° C. for 3 h. The thionyl chloride was then removed by concentration in vacuo. The crude acid chloride was cooled to room temperature, and then dissolved in THF (10 mL). 6-(3-Amino-benzoyl)-1,3-dihydro-indol-2-one (as prepared in Example 40, 0.260 g, 1.03 mmol) was added to the THF solution of the acid chloride, and the mixture was allowed to reflux overnight. The reaction mixture was then allowed to cool to room temperature and filtered. The solid residue was washed with 0° C. THF and collected to afford the 1-Ethyl-5-methyl-1H-pyrazole-4-carboxylic acid [3-(2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide as a solid (0.236 g, 0.61 mmol, 59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07749530B2
Source datasetuspto-grants-2010_07
ORD IDord-859dc74365864f9ab75a0af39bce54de
Source noteuspto-grants-2010_07