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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601816Generated: November 1, 2026

Ethyl Acetate → 6-Chloropyridine-2,3-diamine

https://huagongshe.com/reaction/1601816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantStannous chloride dihydrateHCID 61436—
Reactant6-Chloro-3-nitropyridin-2-ylamineHCID 2724035—
ReactantSodium borohydrideHCID 4311764—
Solventtert-ButanolHCID 6386—
Product6-Chloropyridine-2,3-diamineHCID 1063061565.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 12.0 g of 2-amino-6-chloro-3-nitropyridine, 78.0 g of tin(II) chloride dihydrate and 360 ml of a 9:1 by volume mixture of ethyl acetate and 2-methyl-2-propanol was stirred at 60° C. for 1 hour, after which 1.32 g of sodium borohydride were added at 60° C., and the mixture was stirred for 3 hours at the same temperature. At the end of this time, the reaction mixture was freed from the solvent by distillation under reduced pressure. The resulting residue was diluted with water and neutralized by adding an aqueous solution of potassium carbonate, after which it was extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous sodium sulfate, after which the solvent was removed by distillation under reduced pressure. The residue thus obtained was crystallized by trituration with a mixture of ethyl acetate and hexane, to give 6.50 g of title compound, melting at 120-122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977365
Source datasetuspto-grants-1999_11
ORD IDord-9d9f6cf2fe61424786f410df39e1949a
Source noteuspto-grants-1999_11