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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393747Generated: October 30, 2026

Furan-2-boronic acid → 4-[4-(4-Furan-2-ylphenyl)piperazine-1-sulfonylmethyl]-tetrahydropyran-4carboxylic acid-N-hydroxyamide

https://huagongshe.com/reaction/393747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFuran-2-boronic acidHCID 2734357—
Reactant2-[4-(4-Furan-2-yl-phenyl)piperazine-1-sulfonylmethyl]-3-methylbutyric acidHCID 22646742—
Reactant4-[4-(4-Bromophenyl)piperazine-1-sulfonylmethyl]-tetrahydropyran-4-carboxylic acid hydroxyamideHCID 86584769—
Product4-[4-(4-Furan-2-ylphenyl)piperazine-1-sulfonylmethyl]-tetrahydropyran-4carboxylic acid-N-hydroxyamideHCID 8658477014%

Reaction Steps

Prepared according to the method for the preparation 2-[4-(4-Furan-2-yl-phenyl)piperazine-1-sulfonylmethyl]-3-methylbutyric acid, from 4-[4-(4-bromophenyl)piperazine-1-sulfonylmethyl]tetrahydropyran-4-carboxylic acid hydroxyamide (0.249 g) and furan-2-boronic acid (0.066 g), to give the title compound as a cream solid (0.034 g, 14%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809100B2
Source datasetuspto-grants-2004_10
ORD IDord-01e3b69b729f4a39aeeb0d210da724b6
Source noteuspto-grants-2004_10