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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44634Generated: October 25, 2026

Potassium Carbonate → Pyrazolo[4,3-h]quinazoline-3-carboxamide, 35

https://huagongshe.com/reaction/44634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-[(4-Methylpiperazin-1-yl)methyl]anilineHCID 6484186—
ReactantHCID 86630222HCID 86630222—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
ProductPyrazolo[4,3-h]quinazoline-3-carboxamide, 35HCID 4423611062.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

Pd(OAc)2 (16.34 mg, 0.0728 mmol), (±)-BINAP (45.33 mg, 0.0728 mmol) and dimethylformamide (12 mL) were charged in a round-bottom flask flushed with argon. The mixture was stirred under argon for 30 minutes. Then 3-(4-methyl-piperazin-1-ylmethyl)-phenylamine (448.4 mg, 2.184 mmol), ethyl 8-iodo-1,4,4-trimethyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylic acid methylamide (300 mg, 0.728 mmol), K2CO3 (1.508 g, 10.910 mmol) and dimethylformamide (10 mL) were added. The resulting mixture was heated to 80° C. in an oil bath under argon with good stirring for 3 hours. After cooling to room temperature, the reaction mixture was filtered by suction filtration washing with dichloromethane and the filtrate was evaporated to dryness. The crude was purified by flash chromatography on silica gel (eluant; dichloromethane/methanol 95:5) to afford 215 mg (yield 62%) of pure title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541429B2
Source datasetuspto-grants-2013_09
ORD IDord-46b6f899c1b346f6859ceac5aeae3666
Source noteuspto-grants-2013_09