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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806111Generated: October 31, 2026

Methyl 4-(2-nitropyridin-3-ylthio)benzoate → Methyl 4-(2-aminopyridin-3-ylthio)benzoate

https://huagongshe.com/reaction/1806111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-(2-nitropyridin-3-ylthio)benzoateHCID 66995042—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-(2-aminopyridin-3-ylthio)benzoateHCID 6699470999.6%

Reaction Steps

Added zinc powder (13.88 g, 212.2 mmol) slowly to a solution of methyl 4-(2-nitropyridin-3-ylthio)benzoate (6.16 g, 21.22 mmol) in acetic acid (75 mL) at ambient temperature in an ambient water bath. Stirred for an hour, diluted with dichloromethane, and filtered through celite. Washed the celite pad several times with dichloromethane. Concentrated the filtrate, and partitioned the residue between 2N NaOH and ethyl acetate. The organic layer was washed with water, brine, dried and concentrated to afford the title compound (5.5 g, 99.57% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354540B2
Source datasetuspto-grants-2013_01
ORD IDord-90927b1569c64d86b532574896dd6627
Source noteuspto-grants-2013_01