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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166970Generated: October 25, 2026

(5-Methylthiophen-2-yl)boronic acid → N-[5-(5-methyl-2-thienyl)thiophene-2-sulfonyl]pyrrole

https://huagongshe.com/reaction/1166970

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5-Methylthiophen-2-yl)boronic acidHCID 2734374—
ReactantN-(5-bromothiophenesulfonyl)pyrroleHCID 23445587—
ProductN-[5-(5-methyl-2-thienyl)thiophene-2-sulfonyl]pyrroleHCID 2299847672%

Reaction Steps

N-[5-(5-methyl-2-thienyl)thiophene-2-sulfonyl]pyrrole was prepared in the same manner as described in Example 32C from 2-methyl-thiophene-5-boronic acid and N-(5-bromothiophene-2-sulfonyl)pyrrole. Purification by column chromatography using 2% ether/hexanes gave the pure sulfonamide in 72% yield as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613804B2
Source datasetuspto-grants-2003_09
ORD IDord-dc3069526f0e4e5d9b7ee99f99b47ead
Source noteuspto-grants-2003_09