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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12151Generated: October 26, 2026

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

https://huagongshe.com/reaction/12151

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 21906418100%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 2-amino-5-chloropyridine (328 mg, 2.55 mmol) in tetrahydrofuran (5 ml) was 0.5M potassium bis(trimethylsilyl)amide in toluene (10 ml, 5.05 mmol) dropwise at −78° C. After stirred for additional 0.5 hr at −78° C., the mixture was added 5-chloroisatoic anhydride (0.5 g, 2.55 mmol) at −78° C. The mixture was warmed up to r.t gradually and stirred overnight. After quenched by saturated ammonium chloride solution, the mixture was 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 (0.71 g. 100%). MS found for C12H9Cl2N3O M+=282, (M+2)+=284.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727981B2
Source datasetuspto-grants-2010_06
ORD IDord-a9b6035cb27d4c51a725621d2aa97cec
Source noteuspto-grants-2010_06