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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395355Generated: October 26, 2026

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

https://huagongshe.com/reaction/395355

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 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 quinolinone products.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605617B2
Source datasetuspto-grants-2003_08
ORD IDord-514d000de05942ce995b019c618b5b60
Source noteuspto-grants-2003_08