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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357610Generated: November 2, 2026

Acetonitrile → HCID 68454221, compound

https://huagongshe.com/reaction/2357610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantCesium carbonateHCID 10796—
Reactant6-Bromo-1-chlorophthalazineHCID 22030424—
ReactantHCID 68455343HCID 68455343—
SolventEthyl AcetateHCID 8857—
ProductHCID 68454221HCID 68454221—

Reaction Conditions

Temperature200 °C

Reaction Steps

6-Bromo-1-chlorophthalazine (215 mg, 881 μmol), (R)-N-isopropyl-5-methylpyrrolidine-2-carboxamide (150 mg, 881 μmol), and cesium carbonate (1435 mg, 4405 μmol) were added to acetonitrile (4.4 mL) and heated in the microwave oven for 80 min at 200° C. The reaction was diluted with 75 mL of EtOAc, added to an addition funnel and partitioned with sodium bicarbonate (saturated, aqueous). The organic layer was washed 3× with 50 mL of sodium bicarbonate (saturated, aqueous), separated, dried over sodium sulfate, and concentrated via rotovap to give crude. The crude was purified by chromatography to obtain the title compound. Found MS (ES+): 377(M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759337B2
Source datasetuspto-grants-2010_07
ORD IDord-450ce89441b64eccba7c8502418fc516
Source noteuspto-grants-2010_07