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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353800Generated: October 26, 2026

3-Aminopyridine-2-carbonitrile → HCID 178480640, compound

https://huagongshe.com/reaction/353800

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminopyridine-2-carbonitrileHCID 577015—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 178470776HCID 178470776—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178480640HCID 178480640—

Reaction Conditions

Temperature40 °C

Reaction Steps

LiHMDS (3.6 eq) was added to ethyl [5-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl]acetate (1.0 eq) and 3-aminopyridine-2-carbonitrile (1.0 eq) in THF at 0° C. The reaction was stirred overnight and then heated at 40° C. for 3 hours. The resulting mixture was quenched with an aqueous saturated NH4Cl solution and extracted with EtOAc. The combined organic layers were washed with H2O and brine, dried over Na2SO4, filtered, and concentrated in vacuo to yield a green solid. The crude material was washed successively with CH2Cl2 and MeOH, and then was purified by reverse phase HPLC to provide the desired product. LC/MS m/z 376.1 (MH+), Rt 1.50 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756383B2
Source datasetuspto-grants-2004_06
ORD IDord-0e37607eee534c6a88a584b2dd4318da
Source noteuspto-grants-2004_06