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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445922Generated: October 31, 2026

(4-methoxy-1H-pyrrolo[2,3-b]pyridin-2-yl)methanol → 4-methoxy-2-methyl-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/1445922

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-methoxy-1H-pyrrolo[2,3-b]pyridin-2-yl)methanolHCID 15885418—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Product4-methoxy-2-methyl-1H-pyrrolo[2,3-b]pyridineHCID 11788467—

Reaction Steps

A suspension of (4-methoxy-1H-pyrrolo[2,3-b]pyridin-2-yl)methanol 4 (0.90 g, 5.05 mmol) and Pd(OH)2 (100 mg) in methanol containing 4N aq. HCl solution (10 mL) was hydrogenated under hydrogen pressure (50 psi) for 36 h. The acidic mixture was quenched with 1N NaOH solution. Filtration through celite, concentration and purification on silica gel column using 5% methanol in CH2Cl2 to gave 5 as pale yellow syrup. Yield: 0.68 g, 83%; ESI MS: m/z 163.01 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666898B2
Source datasetuspto-grants-2010_02
ORD IDord-5264f5d2b0c04993aad992605ec1dbed
Source noteuspto-grants-2010_02