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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73801Generated: October 29, 2026

5-Bromo-6-chloropyridine-3-carboxylic acid → 5-bromo-6-chloro-N-(4-(2-chloro-1,1,2,2-tetrafluoroethyl)phenyl)nicotinamide

https://huagongshe.com/reaction/73801

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-6-chloropyridine-3-carboxylic acidHCID 285433—
Reactant4-(2-Chloro-1,1,2,2-tetrafluoroethyl)anilineHCID 86702632—
Product5-bromo-6-chloro-N-(4-(2-chloro-1,1,2,2-tetrafluoroethyl)phenyl)nicotinamideHCID 86702631—

Reaction Steps

The title compound was prepared in an analogous fashion to that described in Stage 9.3 using 5-bromo-6-chloronicotinic acid and 4-(2-chloro-1,1,2,2-tetrafluoroethyl)aniline (Stage 31.3) to afford a beige crystalline powder. HPLC (Condition 4) tR=6.77 min, UPLC-MS (Condition 3) tR=1.31 min, m/z=444.8 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829195B2
Source datasetuspto-grants-2014_09
ORD IDord-0369f5ad220144d7819f55ffbc4cc4f3
Source noteuspto-grants-2014_09