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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352923Generated: October 26, 2026

5-Chloro-1-methyl-1H-pyrazole-4-carbonyl chloride → 5-Chloro-1-methyl-1H-pyrazole-4-carboxylic acid [3-(2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide

https://huagongshe.com/reaction/2352923

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-1-methyl-1H-pyrazole-4-carbonyl chlorideHCID 2735773—
Reactant6-(3-Amino-benzoyl)-1,3-dihydro-indol-2-oneHCID 59256478—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-1-methyl-1H-pyrazole-4-carboxylic acid [3-(2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amideHCID 8661042371.4%

Reaction Steps

A dry flask was charged with 5-Chloro-1-methyl-1H-pyrazole-4-carbonyl chloride (0.200 g, 1.1 mmol) was dissolved in THF (10 mL). 6-(3-Amino-benzoyl)-1,3-dihydro-indol-2-one (as prepared in Example 40, 0.178 g, 0.706 mmol) was added to the THF solution of the acid chloride, and the mixture was allowed to reflux for overnight. The reaction mixture was then allowed to cool to room temperature. The room temperature reaction mixture was filtered. The solid residue was washed with 0° C. THF (10 mL) to afford the 5-Chloro-1-methyl-1H-pyrazole-4-carboxylic acid [3-(2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide as a solid (0.199 g, 0.504 mmol, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07749530B2
Source datasetuspto-grants-2010_07
ORD IDord-45f9bb5ec18145798dea85a255f2e76d
Source noteuspto-grants-2010_07