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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359767Generated: November 2, 2026

5-(2,6-Difluoro-phenylmethanesulfonyl)-1,3-dihydro-indol-2-one → 3-[1-[4-((s)-2-Cyclopropylaminomethyl-pyrrolidine-1-carbonyl)-3,5-dimethyl-1h-pyrrol-2-yl]-meth-(z)-ylidene]-5-(2,6-difluoro-phenylmethanesulfonyl)-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/1359767

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(2,6-Difluoro-phenylmethanesulfonyl)-1,3-dihydro-indol-2-oneHCID 18179931—
Reactant4-((S)-2-cyclopropylaminomethyl-pyrrolidine-1-carbonyl)-3,5-dimethyl-1H-pyrrole-2-carbaldehydeHCID 86588615—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
Product3-[1-[4-((s)-2-Cyclopropylaminomethyl-pyrrolidine-1-carbonyl)-3,5-dimethyl-1h-pyrrol-2-yl]-meth-(z)-ylidene]-5-(2,6-difluoro-phenylmethanesulfonyl)-1,3-dihydro-indol-2-oneHCID 59077758—

Reaction Steps

A mixture of 5-(2,6-difluoro-phenylmethanesulfonyl)-1,3-dihydro-indol-2-one (280 mg, 0.87 mmol), 4-((S)-2-cyclopropylaminomethyl-pyrrolidine-1-carbonyl)-3,5-dimethyl-1H-pyrrole-2-carbaldehyde (250 mg, 0.86 mmol) and piperidine (2 drops) in ethanol (2 mL) was stirred at rt for 4 days. The reaction was concentrated and purified on a silica gel column to give the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599902B2
Source datasetuspto-grants-2003_07
ORD IDord-85377515695449c09b1221ba117aaa9c
Source noteuspto-grants-2003_07