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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221041Generated: October 27, 2026

3-Aminopyridine-4-carbonitrile → HCID 178480638, compound

https://huagongshe.com/reaction/2221041

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminopyridine-4-carbonitrileHCID 10678219—
ReactantHCID 178470776HCID 178470776—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178480638HCID 178480638—

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-aminopyridine4-carbonitrile (1.0 eq) in THF at 0° C. The reaction was stirred overnight. 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 376.3 (MH+), Rt 1.70 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368459B2
Source datasetuspto-grants-2008_05
ORD IDord-1c8ad752a456424cabc15b77eb9b16b2
Source noteuspto-grants-2008_05