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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044302Generated: October 30, 2026

Lithium borohydride → HCID 58577698, compound

https://huagongshe.com/reaction/1044302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
Reactantethyl {2-[(4-nitrophenyl)amino]-3H-imidazo[4,5-b]pyridin-3-yl}acetateHCID 70168453—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58577698HCID 5857769869.7%

Reaction Steps

To a suspension of ethyl {2-[(4-nitrophenyl)amino]-3H-imidazo[4,5-b]pyridin-3-yl}acetate (3.6 g) in THF (120 mL) was added lithium borohydride (0.77 g) at room temperature, and the mixture was refluxed for 2 h. The mixture was cooled to room temperature, quenched with water and extracted with AcOEt. The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel, eluted with 50%-100% AcOEt in hexane) to give the title compound (2.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563575B2
Source datasetuspto-grants-2013_10
ORD IDord-d49457e3b89042a28907edab1bfcbdda
Source noteuspto-grants-2013_10