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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852221Generated: October 30, 2026

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

https://huagongshe.com/reaction/852221

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 numberUS07253181B2
Source datasetuspto-grants-2007_08
ORD IDord-3f246d27dd7145319b2e8141e59286d5
Source noteuspto-grants-2007_08