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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190656Generated: October 29, 2026

2,4-Dioxo-5-thiazolidineacetic acid → 6-{4-[2-(2,4-Dioxo-thiazolidin-5-yl)-acetyl]-piperazin-1-yl}-N-(3-iodo-4-methyl-phenyl)-nicotinamide

https://huagongshe.com/reaction/2190656

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dioxo-5-thiazolidineacetic acidHCID 645030—
ReactantN-(3-Iodo-4-methyl-phenyl)-6-piperazin-1-yl-nicotinamideHCID 59318071—
Reactant4-{4-[5-(3-tert-Butyl-phenylcarbamoyl)-pyridin-2-yl]-piperazine-1-carbonyl}-cyclohexanecarboxylic acid methyl esterHCID 59318085—
Product6-{4-[2-(2,4-Dioxo-thiazolidin-5-yl)-acetyl]-piperazin-1-yl}-N-(3-iodo-4-methyl-phenyl)-nicotinamideHCID 59318143—

Reaction Steps

6-{4-[2-(2,4-Dioxo-thiazolidin-5-yl)-acetyl]-piperazin-1-yl}-N-(3-iodo-4-methyl-phenyl)-nicotinamide was synthesized by the ECDI coupling of N-(3-iodo-4-methyl-phenyl)-6-piperazin-1-yl-nicotinamide and 2-(2,4-dioxo-thiazolidin-5-yl)-acetic acid in a manner similar to the one described in the synthesis of 4-{4-[5-(3-tert-butyl-phenylcarbamoyl)-pyridin-2-yl]-piperazine-1-carbonyl}-cyclohexanecarboxylic acid methyl ester, above. LCMS calcd for C22H22IN5O4S (m/e) 579, obsd 580 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324385B2
Source datasetuspto-grants-2012_12
ORD IDord-9aac2efc200b4418925e511dba85aa52
Source noteuspto-grants-2012_12