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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271546Generated: November 3, 2026

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

https://huagongshe.com/reaction/1271546

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 numberUS07205407B2
Source datasetuspto-grants-2007_04
ORD IDord-912e9c4e51bc4a20949bfd3274941d9c
Source noteuspto-grants-2007_04