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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790056Generated: October 31, 2026

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

https://huagongshe.com/reaction/1790056

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 numberUS07071208B2
Source datasetuspto-grants-2006_07
ORD IDord-77a3b44cb285441d922bff942b3398e8
Source noteuspto-grants-2006_07