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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987914Generated: November 2, 2026

4-(4-Chlorophenyl)-1H-pyrrole-2-carboxylic acid → 4-(4-chlorophenyl)-N-(3-methoxy-4-(2-(tetrahydrofuran-2-yl)ethoxy)phenyl)-1H-pyrrole-2-carboxamide

https://huagongshe.com/reaction/1987914

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Chlorophenyl)-1H-pyrrole-2-carboxylic acidHCID 12897099—
Reactant3-Methoxy-4-(2-(tetrahydrofuran-2-yl)ethoxy)anilineHCID 65158956—
Product4-(4-chlorophenyl)-N-(3-methoxy-4-(2-(tetrahydrofuran-2-yl)ethoxy)phenyl)-1H-pyrrole-2-carboxamideHCID 6721518698%

Reaction Steps

Acylation of 3-methoxy-4-(2-(tetrahydrofuran-2-yl)ethoxy)aniline from step A with 4-(4-chlorophenyl)-1H-pyrrole-2-carboxylic acid to generate the title compound in 98% yield was achieved via the procedure described in step C of Example 1. The crude product was used for next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553836B2
Source datasetuspto-grants-2009_06
ORD IDord-90d00f4495444fa9b6cbb05ffe56a3a3
Source noteuspto-grants-2009_06