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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233947Generated: October 30, 2026

1-(3-Nitropyridin-2-yl)piperidin-4-amine hydrochloride → 4-Bromo-5-Methyl-N-[1-(3-Nitropyridin-2-Yl)piperidin-4-Yl]-1h-Pyrrole-2-Carboxamide

https://huagongshe.com/reaction/2233947

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Nitropyridin-2-yl)piperidin-4-amine hydrochlorideHCID 45789003—
ReactantPentafluorophenyl 4-bromo-5-methyl-1H-pyrrole-2-carboxylateHCID 86608241—
SolventDimethylacetamideHCID 31374—
Product4-Bromo-5-Methyl-N-[1-(3-Nitropyridin-2-Yl)piperidin-4-Yl]-1h-Pyrrole-2-CarboxamideHCID 54759160—

Reaction Steps

1-(3-Nitropyridin-2-yl)piperidin-4-amine hydrochloride salt (Intermediate 39) (41 mg, 1.35 mmol) and TEA (37 μl, 1.35 mmol) were added to pentafluorophenyl 4-bromo-5-methyl-1H-pyrrole-2-carboxylate (Intermediate 17): (50 mg, 1.35 mmol) in anhydrous DMA (1 ml). The mixture was stirred at room temperature overnight. The crude mixture was filtered and purified by semi-preparative HPLC using CH3CN/H2O (0.1% TFA) to yield the title compound as a yellow solid (26 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709503B2
Source datasetuspto-grants-2010_05
ORD IDord-d356dc843460494e91e6541221928ed9
Source noteuspto-grants-2010_05