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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108387Generated: October 31, 2026

HCID 67213401, compound → HCID 67212990, compound

https://huagongshe.com/reaction/2108387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67213401HCID 67213401—
SolventMethanolHCID 887—
SolventAmmonia methanolHCID 21705897—
ProductHCID 67212990HCID 6721299059%

Reaction Steps

A stirred solution of 2-nitro-3-(2-methyl-4-pyridinyl)-1H-imidazole (3.40 g, 16.6 mmol) in 7N methanol/NH3 (70 ml) and methanol (70 ml) was hydrogenated at room temperature on Raney Nickel (2.9 g) for 2 h. The catalyst was removed by filtration and the solution evaporated. The crude product was purified by column chromatography on silica gel (dichloromethane/methanol/NH4OH 40:10:1) to yield 2-amino-3-(2-methyl-4-pyridinyl)-1H-imidazole (1.71 g, 59%) as a green solid. MS (ISP) 175.1 [(M+H)+]; mp 167° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514443B2
Source datasetuspto-grants-2009_04
ORD IDord-077fda0e2f3346acb7298673c3c86c92
Source noteuspto-grants-2009_04