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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649143Generated: November 3, 2026

2-(Methylthio)-5-nitropyridine → HCID 178503249, compound

https://huagongshe.com/reaction/1649143

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Methylthio)-5-nitropyridineHCID 4439313—
ReactantSodium monohydrateHCID 71353970—
ReactantHCID 178526811HCID 178526811—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178503249HCID 178503249—

Reaction Steps

4.5 gm (0.0264 mol) of 2-methylthio-5-nitro-pyridine were hydrogenated at 50° C. and 5 bars pressure in ethanol in the presence of Raney nickel as the catalyst. After the catalyst had been filtered off and after evaporation of the filtrate in vacuo an oil was obtained. A solution of 6.84 gm (0.032 mol) of the sodium monohydrate salt of 2-chloro-4-hydroxy-5-nitro pyrimidine in 150 ml of water was added to the solution of this oil in water. The aqueous solution was heated for 30 minutes on a steam bath, and the resulting precipitate suction-filtered off, washed with water and dried. 4-Hydroxy-2-(6'-methylmercapto-3-pyridyl)amino-5-nitro-pyrimidine was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04415566
Source datasetuspto-grants-1983_11
ORD IDord-22a7ba523a2e4ba2a0151622d806e013
Source noteuspto-grants-1983_11