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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911864Generated: October 31, 2026

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

https://huagongshe.com/reaction/911864

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 numberUS08022223B2
Source datasetuspto-grants-2011_09
ORD IDord-8c32ef8a3cb54c7b8698674ac93061a5
Source noteuspto-grants-2011_09