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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815348Generated: October 29, 2026

N-methyl-2-oxoindoline-5-sulfonamide → HCID 67282724, compound

https://huagongshe.com/reaction/1815348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-oxoindoline-5-sulfonamideHCID 10176909—
ReactantHCID 85786887HCID 85786887—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
ProductHCID 67282724HCID 67282724—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 5-methylaminosulfonyl-2-oxindole (0.06 g, 0.22 mmol), [(5-formyl-4-methyl-1H-pyrrole-3-carbonyl)-amino]-acetic acid ethyl ester (0.075 g, 0.27 mmol) and piperidine (2 drops) in ethanol (5 mL) was heated in a sealed tube at 90° C. for 12 hrs. After cooling, the precipitate was collected by vacuum filtration, washed with ethanol, triturated with dichloromethane/ether and dried to give 0.035 g (36%), of the title compound as a yellowish brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878733B1
Source datasetuspto-grants-2005_04
ORD IDord-e3919d75a9f24e218cf99e724534e521
Source noteuspto-grants-2005_04