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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233959Generated: October 30, 2026

4-Bromo-5-methyl-1H-pyrrole-2-carboxylic acid → N-[1-(4-Acetyl-6-chloro-2-pyridinyl)-4-piperidinyl]-4-bromo-5-methyl-1H-pyrrole-2-carboxamide

https://huagongshe.com/reaction/2233959

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-5-methyl-1H-pyrrole-2-carboxylic acidHCID 68518222—
Reactant1-[2-(4-Aminopiperidin-1-yl)-6-chloropyridin-4-yl]ethanone hydrochloride saltHCID 86608314—
ProductN-[1-(4-Acetyl-6-chloro-2-pyridinyl)-4-piperidinyl]-4-bromo-5-methyl-1H-pyrrole-2-carboxamideHCID 86608317—

Reaction Steps

The title compound was synthesized by an analogous method to Example 42 starting from 1-1-[2-(4-aminopiperidin-1-yl)-6-chloropyridin-4-yl]ethanone hydrochloride salt (Intermediate 197) and 4-Bromo-5-methyl-1H-pyrrole-2-carboxylic acid (Intermediate 18).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709503B2
Source datasetuspto-grants-2010_05
ORD IDord-3ce457e4f6f74459846a3579f6b24ac2
Source noteuspto-grants-2010_05