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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914739Generated: October 26, 2026

2'-Aminoacetophenone → 8-[(2-acetylphenyl)amino]-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide

https://huagongshe.com/reaction/1914739

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2'-AminoacetophenoneHCID 11086—
ReactantPotassium CarbonateHCID 11430—
Reactant8-iodo-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamideHCID 44235652—
SolventDimethylformamideHCID 6228—
Product8-[(2-acetylphenyl)amino]-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamideHCID 4688695747%

Reaction Steps

Palladium acetate Pd(OAc)2 (20 mg, 0.09 mmol), (±)-BINAP (55 mg, 0.09 mmol) and dimethylformamide (5 mL) were charged in a round-bottom flask flushed with argon. The flask was evacuated and backfilled with argon. The mixture was stirred under argon for 30 minutes and added to a mixture of 2-acetylaniline (0.162 ml, 1.35 mmol), 8-iodo-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide (319 mg, 0.9 mmol), potassium carbonate (1.24 g, 9 mmol) in dimethylformamide (10 mL). The resulting mixture was stirred at 80° C. for 4 hours under argon. After cooling to room temperature, the reaction mixture was filtered on a pad of celite. The solvent was concentrated, the crude solid was purified by flash chromatography on silica gel (eluant: DCM/EtOH 90/10) to afford 153 mg (47% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614220B2
Source datasetuspto-grants-2013_12
ORD IDord-e8405148e21a41c39871e51a205faa3e
Source noteuspto-grants-2013_12