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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233938Generated: October 30, 2026

Pentafluorophenyl 4-bromo-5-methyl-1H-pyrrole-2-carboxylate → Methyl 2-(4-{[(4-bromo-5-methyl-1H-pyrrol-2-yl)carbonyl]amino}piperidin-1-yl)-6-chloroisonicotinate

https://huagongshe.com/reaction/2233938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentafluorophenyl 4-bromo-5-methyl-1H-pyrrole-2-carboxylateHCID 86608241—
ReactantMethyl 2-(4-aminopiperidin-1-yl)-6-chloroisonicotinate hydrochloride saltHCID 86608260—
SolventDimethylacetamideHCID 31374—
ProductMethyl 2-(4-{[(4-bromo-5-methyl-1H-pyrrol-2-yl)carbonyl]amino}piperidin-1-yl)-6-chloroisonicotinateHCID 8660828776.1%

Reaction Steps

Pentafluorophenyl 4-bromo-5-methyl-1H-pyrrole-2-carboxylate (intermediate 17, 1.81 g, 4.90 mmol) and TEA (682 μl, 4.9 mmol) were added to methyl 2-(4-aminopiperidin-1-yl)-6-chloroisonicotinate hydrochloride salt (Intermediate 93; 1.5 g, 4.90 mmol) in anhydrous DMA (10 ml). The mixture was stirred at room temperature 18 h then partitioned between EtOAc and water. The organic layer was washed with water, dried over Na2SO4 and concentrated under vacuum. The solid material was purified by flash chromatography eluting with EtOAc/n-hexanes mixture (7:3) to give the title compound as a brown solid (1.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709503B2
Source datasetuspto-grants-2010_05
ORD IDord-beee9fc68d4e46b4b3a3e740a012238d
Source noteuspto-grants-2010_05