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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896731Generated: November 1, 2026

Toluene → 2-Amino-5-chloro-N-(5-chloropyridin-2-yl)benzamide

https://huagongshe.com/reaction/1896731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant2-Amino-5-chloropyridineHCID 66174—
Reactant5-Chloroisatoic anhydrideHCID 78480—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-5-chloro-N-(5-chloropyridin-2-yl)benzamideHCID 21906418—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 2-amino-5-chloropyridine (787 mg, 6.1 mmol) in tetrahydrofuran (5 ml) was added 0.5M potassium bis(trimethylsilyl)amide in toluene (20 ml, 10.1 mmol) dropwise at −78° C. After stirred for additional 0.5 hr at −78° C., the mixture was added 5-chloroisatoic anhydride (1 g, 5.1 mmol) at −78° C. The mixture was warmed up to r.t gradually and stirred overnight. After concentrated, the crude was washed with saturated ammonium chloride solution and extracted by ethyl acetate. The organic layer was dried over magnesium sulfate and concentrated to give (2-amino-5-chlorophenyl)-N-(5-chloro(2-pyridyl))carboxamide as yellow solid (1.39 g. 99%). MS found for C12H9Cl2N30 M+=282, (M+2)+=284.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518977B2
Source datasetuspto-grants-2013_08
ORD IDord-42bf7a59ffb94eaa8381c69da71c088a
Source noteuspto-grants-2013_08