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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911238Generated: November 1, 2026

2-hydroxymethyl-6-nitro-3-methyl-3H-imidazo[4,5-b]pyridine → (6-Amino-3-methyl-3H-imidazo[4,5-b]pyridin-2-yl)methanol

https://huagongshe.com/reaction/1911238

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-hydroxymethyl-6-nitro-3-methyl-3H-imidazo[4,5-b]pyridineHCID 66888046—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Product(6-Amino-3-methyl-3H-imidazo[4,5-b]pyridin-2-yl)methanolHCID 668887270.1%

Reaction Steps

A suspension of 0.5 g (2.4 mol) of 2-hydroxymethyl-6-nitro-3-methyl-3H-imidazo[4,5-b]pyridine, prepared in the preceding step, and 0.3 g of 10% palladium-on-charcoal is stirred for 3 hours under 2.5 atm. of hydrogen. After this time, the suspension is filtered through a pad of Celite and the filtrate is concentrated under reduced pressure. 0.4 g of the expected product is thus isolated, and is used without further purification in the rest of the synthesis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604050B2
Source datasetuspto-grants-2013_12
ORD IDord-5fb678b4d87c4eb7b6eec2a815e62c02
Source noteuspto-grants-2013_12