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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584824Generated: November 2, 2026

2-(p-Toluenesulfonyl)-5-tributylstannylisoindoline → Ethyl 1-cyclopropyl-6-fluoro-8-methyl-7-[2-(p-toluenesulfonyl)isoindolin-5-yl]-1,4-dihydro-4-oxoquinoline-3-carboxylate

https://huagongshe.com/reaction/1584824

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(p-Toluenesulfonyl)-5-tributylstannylisoindolineHCID 15870854—
ReactantHCID 21220308HCID 21220308—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductEthyl 1-cyclopropyl-6-fluoro-8-methyl-7-[2-(p-toluenesulfonyl)isoindolin-5-yl]-1,4-dihydro-4-oxoquinoline-3-carboxylateHCID 15870841—

Reaction Steps

In 1 ml of toluene was suspended 47 mg of ethyl 7-bromo-1-cyclopropyl-6-fluoro-8-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylate, and to this suspension were added 74 mg of 2-(p-toluenesulfonyl)-5-tributylstannylisoindoline and 1.5 mg of tetrakis(triphenylphosphine)palladium (0), after which the resulting mixture was heated under reflux for 18 hours under a nitrogen atmosphere. The reaction mixture was concentrated under reduced pressure, and the residue obtained was purified by a column chromatography (eluent: n-hexane:ethyl acetate=1:1), and diethyl ether was then added thereto, after which the crystals formed were collected by filtration, to obtain 27 mg of colorless, crystalline ethyl 1-cyclopropyl-6-fluoro-8-methyl-7-[2-(p-toluenesulfonyl)isoindolin-5-yl]-1,4-dihydro-4-oxoquinoline-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05935952
Source datasetuspto-grants-1999_08
ORD IDord-8800f2f5f56d4e2ab1947337aa3e271f
Source noteuspto-grants-1999_08