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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73772Generated: October 25, 2026

5-Bromo-6-chloropyridine-3-carboxylic acid → 5-bromo-6-chloro-N-(4-(pentafluorosulfanyl)phenyl)nicotinamide

https://huagongshe.com/reaction/73772

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-6-chloropyridine-3-carboxylic acidHCID 285433—
Reactant4-Aminophenylsulphur pentafluorideHCID 2779190—
Product5-bromo-6-chloro-N-(4-(pentafluorosulfanyl)phenyl)nicotinamideHCID 86702616—

Reaction Steps

The title compound was prepared in an analogous fashion to that described in Stage 11.2 using 5-bromo-6-chloro-nicotinic acid and 4-aminophenylsulfur pentafluoride to afford an orange solid. HPLC (Condition 4), tR=6.43 min, UPLC-MS (Condition 3), tR=1.27 min, m/z=435.3/437.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829195B2
Source datasetuspto-grants-2014_09
ORD IDord-f540ade1c2734011a562675160fdfe27
Source noteuspto-grants-2014_09