Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64174Generated: October 26, 2026

Nitrogen → N-(3-(3-fluoropyridin-2-yl)-5-nitrophenyl)acetamide

https://huagongshe.com/reaction/64174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
Reactant2-Chloro-3-fluoropyridineHCID 2782791—
Reactant3-Nitro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl-acetamideHCID 131737215—
CatalystHCID 178477754HCID 178477754—
ProductN-(3-(3-fluoropyridin-2-yl)-5-nitrophenyl)acetamideHCID 8950032170%

Reaction Steps

A solution of N-(3-nitro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl-acetamide (10 g, 32.67 mmol) in 1,2-dimethoxyethane (100 ml) was degassed by N2 bubbling for 5 min. 2-Chloro-3-fluoro pyridine (4.29 g, 32.67 mmol) was added and the mixture was degassed for another 5 min. Pd(dppf)cl2 (2.6 g, 3.26 mmol) and aqueous sodium carbonate (10.39 g, 98.03 mmol) were added and the procedure of Example 1(d) was followed. The crude residue of the product was purified by column chromatography (60-120 silica gel, 3% methanol in chloroform) to yield the title product in 70% yield (6.3 g). 1H NMR (300 MHz, DMSO-d6): δ10.64 (s, 1H), 8.74 (m, 1H), 8.62 (m, 1H), 8.55, (brs, 1H), 8.44 (brs, 1H), 7.93 (m, 1H), 7.60 (m, 1H), 2.12 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447091B2
Source datasetuspto-grants-2016_09
ORD IDord-3beae237025b4131ad50a76acee9cc57
Source noteuspto-grants-2016_09