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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397701Generated: October 26, 2026

5-[(1,3-dioxo-2,3-dihydro-1H-2-isoindolyl)methyl]-2-furoic acid → [(Z)-[amino-[(2S)-1-(cyclohexylmethylsulfonyl)piperidin-2-yl]methylidene]amino] 5-[(1,3-dioxoisoindol-2-yl)methyl]furan-2-carboxylate

https://huagongshe.com/reaction/397701

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-[(1,3-dioxo-2,3-dihydro-1H-2-isoindolyl)methyl]-2-furoic acidHCID 23000701—
ReactantHCID 59085897HCID 59085897—
Product[(Z)-[amino-[(2S)-1-(cyclohexylmethylsulfonyl)piperidin-2-yl]methylidene]amino] 5-[(1,3-dioxoisoindol-2-yl)methyl]furan-2-carboxylateHCID 59085909—

Reaction Steps

The title compound was prepared by a similar method to Preparation 5 from (Z)-(2S)-1-[(cyclohexylmethyl)sulfonyl]-N′2-hydroxy-2-piperidinecarboximidamide [see Preparation 28] and 5-[(1,3-dioxo-2,3-dihydro-1H-2-isoindolyl)methyl]-2-furoic acid (see Preparation 98], to afford (Z)-(2S)-1-[(cyclohexylmethyl)sulfonyl]-N′2-[(5-[(1,3-dioxo-2,3-dihydro-1H-2-isoindolyl)methyl]-2-furylcarbonyl)oxy]-2-piperidinecarboximidamide as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610707B1
Source datasetuspto-grants-2003_08
ORD IDord-3f143839cf044ab98abd08d740ed41a3
Source noteuspto-grants-2003_08