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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722162Generated: October 30, 2026

4-Aminopyridine-3-carbonitrile → HCID 178507213, compound

https://huagongshe.com/reaction/722162

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminopyridine-3-carbonitrileHCID 577016—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 178470777HCID 178470777—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178507213HCID 178507213—

Reaction Steps

LiHMDS (3.3 eq) was added to ethyl (5-morpholin-4-yl-1H-benzimidazol-2-yl)acetate (1.0 eq) and 4-aminopyridine-3-carbonitrile (see J. Chem. Soc. 1967, p 1558–1564; 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 brown 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 363.2 (MH+), Rt 1.55 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138409B2
Source datasetuspto-grants-2006_11
ORD IDord-45f647adc99b4c9ba34a40f6999ae76e
Source noteuspto-grants-2006_11