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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007100Generated: October 26, 2026

3-Nitrophenylboronic Acid → 2-Ethyl-7-(3-nitro-phenyl)-4H-benzo[1,4]thiazin-3-one

https://huagongshe.com/reaction/1007100

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitrophenylboronic AcidHCID 1677—
ReactantPotassium CarbonateHCID 11430—
Reactant7-bromo-2-ethyl-4H-benzo[1,4]thiazin-3-oneHCID 22667748—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-Ethyl-7-(3-nitro-phenyl)-4H-benzo[1,4]thiazin-3-oneHCID 98833227.4%

Reaction Steps

A solution of 7-bromo-2-ethyl-4H-benzo[1,4]thiazin-3-one (2 g, 7.3 mmol), 3-nitrophenyl boronic acid (1.22 g, 7.3 mmol), potassium carbonate (3 g, 22 mmol), and tetrakis(triphenylphosphine)palladium(0) (0.84 g, 0.72 mmol) in dimethoxyethane (100 ml), ethanol (25 ml), and water (25 ml) was heated to reflux for 6 hours. After cooling to room temperature, the mixture was diluted with water and extracted with EtOAc (3×40 mL). The combined organic extracts were washed with water, then brine, dried (MgSO4) and evaporated. The residue was recrystallized from ethanol to afford the title compound as tan crystals (0.17 g, 7.3%): mp 180° C.; MS (EI) m/z 314 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794373B2
Source datasetuspto-grants-2004_09
ORD IDord-35771439dda347bd803c68a50697ec29
Source noteuspto-grants-2004_09