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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392631Generated: October 26, 2026

2-Aminobenzonitrile → 4-Aminoquinoline

https://huagongshe.com/reaction/392631

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminobenzonitrileHCID 72913—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantBenzimidazole acetateHCID 67199695—
SolventTetrahydrofuranHCID 8028—
Product4-AminoquinolineHCID 68476—

Reaction Steps

LiHMDS (3-4 eq) was added to the benzimidazole acetate (1.0 eq) in THF (at a constant temperature ranging from −78° C. to 0° C.). After 20 minutes, a solution of the 2-aminobenzonitrile (1.1 eq) in THF was then added. The resulting mixture was allowed to warm to room temperature, stirred for 1-3 hours and was then heated to approx. 40° C.-65° C.(1 hour to 12 hours). The mixture was cooled to 0° C. and quenched with NH4Cl (aq, saturated). The aqueous phase was extracted with Ch2Cl2 or EtOAc, and the organic extracts were collected, dried (Na2SO4), and filtered. Evaporation of the solvent under reduced pressure and purification of the residue by silica gel chromatography or HPLC provided the 4-amino quinoline products.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800760B2
Source datasetuspto-grants-2004_10
ORD IDord-cb4a92211ca7435d99b3046171b4a071
Source noteuspto-grants-2004_10