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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983175Generated: October 27, 2026

1,2-Dichloroethane → 4-(3-Fluoro-phenyl)-3-[1-[5-methyl-3-(4-pyrrolidin-1-ylmethyl-piperidine-1-carbonyl)-1h-pyrrol-2-yl]-meth-(z)-ylidene]-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/983175

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(r)-3-Pyrrolidin-1-ylmethyl-piperidineHCID 7183063—
Reactant2-[4-(3-fluoro-phenyl)-2-oxo-1,2-dihydro-indol-(3Z) ylidenemethyl]-5-methyl-1H-pyrrole-3-carboxylic acidHCID 69740587—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
Product4-(3-Fluoro-phenyl)-3-[1-[5-methyl-3-(4-pyrrolidin-1-ylmethyl-piperidine-1-carbonyl)-1h-pyrrol-2-yl]-meth-(z)-ylidene]-1,3-dihydro-indol-2-oneHCID 6006152970%

Reaction Steps

2-[4-(3-Fluoro-phenyl)-2-oxo-1,2-dihydro-indol-(3-Z)-ylidenemethyl]-5-methyl-1H-pyrrole-3-carboxylic acid (108 mg, 0.3 mmol) was coupled with (R)-3-pyrrolidin-1-ylmethyl-piperidine (99 mg, 2 eq.), HOBt (1 eq.), EDC (1.5 eq.) and TEA (3 drops) in THF (1 mL), acetonitrile (1 mL) at rt for overnight to give 107 mg (70%) of the titled compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06861418B2
Source datasetuspto-grants-2005_03
ORD IDord-b6c8d1eb72d94a7d8e47cb5319a6a12b
Source noteuspto-grants-2005_03