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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352878Generated: November 1, 2026

Acetone → 4-chloro-1,3-dimethyl-N-[3-[3-[[4-(4-methylpiperazin-1-yl)anilino]methylidene]-2-oxo-1H-indole-6-carbonyl]phenyl]pyrazole-5-carboxamide

https://huagongshe.com/reaction/2352878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant4-(4-Methylpiperazin-1-yl)anilineHCID 737253—
ReactantHCID 178434051HCID 178434051—
SolventTetrahydrofuranHCID 8028—
Product4-chloro-1,3-dimethyl-N-[3-[3-[[4-(4-methylpiperazin-1-yl)anilino]methylidene]-2-oxo-1H-indole-6-carbonyl]phenyl]pyrazole-5-carboxamideHCID 178434050—

Reaction Conditions

Temperature65 °C

Reaction Steps

A small screw cap test tube was charged with 4-Chloro-2,5-dimethyl-2H-pyrazole-3-carboxylic acid [3-(3-hydroxymethylene-2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide (prepared below, 70 mg, 0.160 mmol) and THF (1.5 mL). To the resulting solution was added 4-(4-methyl-piperazin-1-yl)-phenylamine (30.6 mg, 0.160 mmol), and the mixture was stirred for 24 h at 65° C. Subsequently, the reaction mixture was cooled to room temperature and concentrated in vacuo. The crude residue was dissolved in EtOAc. The resulting solution was diluted with Hexanes to initiate the precipitation of the product. The solid precipitate that formed was filtered then washed with ˜3 mL of acetone yielding 58% (56.7 mg, 0.093 mmol) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07749530B2
Source datasetuspto-grants-2010_07
ORD IDord-abf6026e84734f59bd1563212a7e3ac2
Source noteuspto-grants-2010_07