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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294596Generated: October 30, 2026

2-Amino-5-methoxypyridine → 3-(2-Methyl-2-nitropropyl)-6-methoxyimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1294596

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-methoxypyridineHCID 11320934—
Reactant2-Bromo-4-methyl4-nitropentanalHCID 22038558—
SolventDichloromethaneHCID 6344—
Product3-(2-Methyl-2-nitropropyl)-6-methoxyimidazo[1,2-a]pyridineHCID 2203857442.1%

Reaction Steps

2-Amino-5-methoxypyridine (J. Med. Chem., 24:39, 1981; 2.02 g, 16.3 mmol) and 2-bromo-4-methyl-4-nitropentanal (16.3 mmol) are reacted as described in Amine 7 and the product is isolated in two crops from the concentrated mixture by heating twice with dichloromethane (30 ml and 10 ml) and filtration without further chromatographic purification to give 1.71 g of 3-(2-methyl-2-nitropropyl)-6-methoxyimidazo[1,2-a]pyridine (42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241772B2
Source datasetuspto-grants-2007_07
ORD IDord-5f7b4eaac57242d28f105ec11bacf00c
Source noteuspto-grants-2007_07