Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252271Generated: October 25, 2026

3-Bromo-5-fluoropyridine → N-tert-Butyl-4-(5-fluoro-pyridin-3-yl)-3-methyl-benzenesulfonamide

https://huagongshe.com/reaction/252271

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-5-fluoropyridineHCID 820206—
ReactantHCID 178425957HCID 178425957—
ProductN-tert-Butyl-4-(5-fluoro-pyridin-3-yl)-3-methyl-benzenesulfonamideHCID 6685745856.5%

Reaction Steps

This compound was prepared analogous to Example 52, starting from N-tert-butyl-3-methyl-benzenesulfonamide boronic acid (0.5 g, 1.84 mmol) and 5-bromo-3-fluoropyridine (357 mg, 2.03 mmol, 1.1 equiv.) After purification on silica-gel with n-heptane/ethyl acetate, 335 mg of the title compound were obtained as a light yellow solid MS (ES): m/e 321.1 (M−H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868030B2
Source datasetuspto-grants-2011_01
ORD IDord-98622a2de9ac482d8e71844938101c23
Source noteuspto-grants-2011_01