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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916487Generated: October 31, 2026

Sodium Bicarbonate → N-(2-nitro-6-(pyridin-2-yl)phenyl)acetamide

https://huagongshe.com/reaction/1916487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant2-(Tributylstannyl)pyridineHCID 607784—
ReactantN-(2-bromo-6-nitrophenyl)acetamideHCID 4643062—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductN-(2-nitro-6-(pyridin-2-yl)phenyl)acetamideHCID 8670107092%

Reaction Steps

A degassed mixture of N-(2-bromo-6-nitrophenyl)acetamide (XCI) (4.8 g, 19 mmol, 1.00 eq), 2-(tributylstannyl)pyridine (XCVII) (7.5 g, 20 mmol, 1.05 eq) and Pd(PPh3)4 (2.1 g, 1.8 mmol, 0.01 eq) in toluene (60 mL) was heated to reflux under nitrogen overnight. Saturated sodium bicarbonate solution (50 mL) was then added to the mixture and it was extracted with ethyl acetate (50 mL×3). The combined organic layers were dried over Na2SO4, filtered and concentrated in vacuo, the residue was purified by column chromatography on silica gel (EtOAc:PE=1:2→100% EtOAc) to afford N-(2-nitro-6-(pyridin-2-yl)phenyl)acetamide (XCVIII) (4.4 g, 17.1 mmol, 92% yield) as a white-off solid. 1H NMR (DMSO-d6, 400 MHz) δ ppm 1.93 (s, 3H), 7.43-7.51 (m, 1H), 7.51-7.65 (m, 1H), 7.67 (d, J=7.6 Hz, 1H), 7.97 (dd, J=7.6 Hz, J=2.4 Hz, 3H), 8.75 (d, J=4.4 Hz, 1H), 10.52 (s, 1H); ESIMS found for C13H11N3O3 m/z 258 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618128B1
Source datasetuspto-grants-2013_12
ORD IDord-b347b0e056a64beeabe0be11cb743730
Source noteuspto-grants-2013_12