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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430053Generated: November 3, 2026

Lithium borohydride → HCID 58577698, compound

https://huagongshe.com/reaction/1430053

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 numberUS08940758B2
Source datasetuspto-grants-2015_01
ORD IDord-f65c7e8daa004516a26188d9c3255124
Source noteuspto-grants-2015_01