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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641018Generated: October 30, 2026

Tetrahydrofuran → 5-ethyl-1-methyl-N-[3-[2-oxo-3-[[4-(pyrrolidin-1-ylmethyl)anilino]methylidene]-1H-indole-6-carbonyl]phenyl]pyrazole-3-carboxamide

https://huagongshe.com/reaction/641018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-(Pyrrolidin-1-ylmethyl)anilineHCID 776852—
Reactant5-ethyl-N-[3-[3-(hydroxymethylidene)-2-oxo-1H-indole-6-carbonyl]phenyl]-1-methylpyrazole-3-carboxamideHCID 178436688—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product5-ethyl-1-methyl-N-[3-[2-oxo-3-[[4-(pyrrolidin-1-ylmethyl)anilino]methylidene]-1H-indole-6-carbonyl]phenyl]pyrazole-3-carboxamideHCID 17843668618%

Reaction Conditions

Temperature65 °C

Reaction Steps

A small screw cap test tube was charged with 5-Ethyl-1-methyl-1H-pyrazole-3-carboxylic acid [3-(3-hydroxymethylene-2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide (as prepared in Example 345, 70 mg, 0.1681 mmol) and THF (2.0 mL). To the resulting solution was added 4-Pyrrolidin-1-ylmethyl-phenylamine (30.1 mg, 0.171 mmol), and the mixture was stirred for 24 h at 65° C. Subsequently, the reaction mixture was cooled to room temperature and diluted with EtOAc (˜5 mL) and Hexane (˜40 mL). The solid that precipitated was collected by filtration and washed with 0° C. iPrOH (˜10 mL) affording the title compound in 18% yield (0.018 g, 0.031 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07692005B2
Source datasetuspto-grants-2010_04
ORD IDord-d6e4f936e9e040929d7eaf5f3c0d06f4
Source noteuspto-grants-2010_04