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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115783Generated: October 31, 2026

Potassium Hydroxide → HCID 59813780, compound

https://huagongshe.com/reaction/2115783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantN-(6-Hydroxy-naphthalen-1-yl)-benzamideHCID 67520279—
ReactantHCID 67520397HCID 67520397—
CatalystCopperHCID 23978—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 59813780HCID 59813780—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a microwaveable vial containing 0.300 g (1.1 mmol) of N-(6-hydroxy-naphthalen-1-yl)-benzamide in 1.5 mL DMF and 1.5 mL pyridine, was added 0.771 g (2.8 mmol) of [2-(4-chloro-6-methoxy-quinolin-7-yloxy)-ethyl]-dimethylamine. Then added (5 mmol %) copper grind into the mixture, along with 0.158 g (2.5 mmol) KOH pellets. The vial was heated in a microwave for 18 min at 120° C. (60 Watts constant power, CEM powermax). The mixture was diluted with CH2Cl2 and water, then transferred to seperatory funnel. The organics were extracted 3× with CH2Cl2. The organic layers were combined, dried over Na2SO4, filtered, and concentrated in-vacuo. The crude was purified by reverse-phase HPLC. A tan oil was collected, which was titled product. MS (ESI pos. ion) m/z: 508 (M+H). Calc'd for C31H29N3O4-507.22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435823B2
Source datasetuspto-grants-2008_10
ORD IDord-84f618ebdc134a83a3bd78add9df7ae8
Source noteuspto-grants-2008_10