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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514722Generated: October 26, 2026

n-(5-Bromo(2-pyridyl))(3,4,5-trimethoxy-2-nitrophenyl)carboxamide → (2-Amino-3,4,5-trimethoxyphenyl)-n-(5 bromo(2-pyridyl))carboxamide

https://huagongshe.com/reaction/514722

Reaction equation

Participants

RoleNameHCIDCharge
Reactantn-(5-Bromo(2-pyridyl))(3,4,5-trimethoxy-2-nitrophenyl)carboxamideHCID 22596319—
CatalystHCID 178418476HCID 178418476—
SolventEthyl AcetateHCID 8857—
Product(2-Amino-3,4,5-trimethoxyphenyl)-n-(5 bromo(2-pyridyl))carboxamideHCID 8578382477.7%

Reaction Steps

To a solution of the compound of N-(5-bromo(2-pyridyl))(3,4,5-trimethoxy-2-nitrophenyl)carboxamide (790 mg, 1.92 mmol) in ethyl acetate (5 ml) was added tin chloride (II) hydrate (1.73 g, 7.67 mmol). The mixture was stirred under reflux condition for 2 hrs. After filtered by Celite, the filtrate was added 1N sodium hydroxide solution and extracted with ethyl acetate. The organic layer was dried over magnesium sulfate and concentrated to give (2-amino-3,4,5-trimethoxyphenyl)-N-(5-bromo(2-pyridyl))carboxamide (570 mg, 77%). MS found for C15H16BrN3O4 M+=382, (M+2)+=384.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108922B2
Source datasetuspto-grants-2015_08
ORD IDord-cebf6d999fb54efda168bf6643d08c58
Source noteuspto-grants-2015_08