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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353802Generated: October 25, 2026

ethyl 2-(1H-1,3-benzodiazol-2-yl)acetate → 4-Amino-5-(1H-benzimidazol-2-yl)thieno[2,3-b]pyridin-6(7H)-one

https://huagongshe.com/reaction/353802

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl 2-(1H-1,3-benzodiazol-2-yl)acetateHCID 308071—
Reactant2-Aminothiophene-3-carbonitrileHCID 736607—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTetrahydrofuranHCID 8028—
Product4-Amino-5-(1H-benzimidazol-2-yl)thieno[2,3-b]pyridin-6(7H)-oneHCID 135839372—

Reaction Steps

LiHMDS (4.3 eq) was added to ethyl 1H-benzimidazol-2-ylacetate (1.1 eq) and 2-aminothiophene-3-carbonitrile (1.0 eq) in THF at 0° C. After 1 hour, the resulting mixture was warmed to room temperature and then stirred overnight. The mixture was quenched with an aqueous saturated NH4Cl solution and extracted with EtOAc. The organic layer was washed with H2O and brine, dried over Na2SO4, filtered, and concentrated in vacuo to yield a brown solid. LC/MS m/z 283.1 (MH+), Rt 1.88 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756383B2
Source datasetuspto-grants-2004_06
ORD IDord-783148e0d98243fbb8fbb1c354743431
Source noteuspto-grants-2004_06