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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722166Generated: October 27, 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/722166

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 numberUS07138409B2
Source datasetuspto-grants-2006_11
ORD IDord-ae39339c140045bab3f28cb9297c81c8
Source noteuspto-grants-2006_11