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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10560Generated: October 26, 2026

Water → 4-(4-Methoxy-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidine

https://huagongshe.com/reaction/10560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium MethoxideHCID 10942334—
Reactant4-(4-Bromo-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 21979972—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventMethanolHCID 887—
SolventPyridineHCID 1049—
Product4-(4-Methoxy-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 21979974—

Reaction Conditions

Temperature65 °C

Reaction Steps

A suspension of Intermediate 71 (600 mg) and copper(I) iodide (141 mg, Kanto Chemicals) in methanol (5.5 ml) and pyridine (5.5 ml) was added with sodium methoxide (28% methanol solution, 1.7 ml, Wako Pure Chemical Industries) and stirred with heating at 65° C. for 24 hours. The reaction mixture was cooled to room temperature, then added with water (30 ml) and extracted three times with ethyl acetate (20 ml for each time). The combined organic layer was washed twice with saturated brine (30 ml for each time) and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:2) to obtain the title compound (364 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094789B2
Source datasetuspto-grants-2006_08
ORD IDord-e66b85a64f8c49938e94e99c298be080
Source noteuspto-grants-2006_08