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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817252Generated: October 26, 2026

2-Aminobenzonitrile → 4-Amino-1,2-dihydroquinolin-2-one

https://huagongshe.com/reaction/1817252

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminobenzonitrileHCID 72913—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantBenzimidazole acetateHCID 67199695—
SolventTetrahydrofuranHCID 8028—
Product4-Amino-1,2-dihydroquinolin-2-oneHCID 459666—

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 0C). 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 quinolinone products.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598268B2
Source datasetuspto-grants-2009_10
ORD IDord-3db41689373f4f748c0ace9b07588deb
Source noteuspto-grants-2009_10