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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221043Generated: October 26, 2026

3-Aminopyridine-2-carbonitrile → HCID 178482919, compound

https://huagongshe.com/reaction/2221043

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminopyridine-2-carbonitrileHCID 577015—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 178470775HCID 178470775—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178482919HCID 178482919—

Reaction Conditions

Temperature40 °C

Reaction Steps

LiHMDS (3.6 eq) was added to ethyl {5-[3-(dimethylamino)pyrrolidin-1-yl]-1H-benzimidazol-2-yl}acetate (1.0 eq) and 3-aminopyridine-2-carbonitrile (J. Org. Chem. 1958, 1616-1617; 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 390.2 (MH+), Rt 1.79 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368459B2
Source datasetuspto-grants-2008_05
ORD IDord-7f7bf868039d41939a540730437d577d
Source noteuspto-grants-2008_05