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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927283Generated: October 31, 2026

Potassium Carbonate → tert-butyl 5-(2-(4-fluorophenyl)-6-(N'-hydroxycarbamimidoyl)-1-oxo-1,2-dihydroisoquinolin-3-yl)pentanoate

https://huagongshe.com/reaction/927283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantTert-butyl 5-(6-cyano-2-(4-fluorophenyl)-1-oxo-1,2-dihydroisoquinolin-3-yl)pentanoateHCID 118558143—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Producttert-butyl 5-(2-(4-fluorophenyl)-6-(N'-hydroxycarbamimidoyl)-1-oxo-1,2-dihydroisoquinolin-3-yl)pentanoateHCID 90095090100.2%

Reaction Steps

Hydroxylamine hydrochloride (183 mg, 2.64 mmol) was added to a stirred, room temperature mixture of tert-butyl 5-(6-cyano-2-(4-fluorophenyl)-1-oxo-1,2-dihydroisoquinolin-3-yl)pentanoate (185 mg, 0.440 mmol) and K2CO3 (365 mg, 2.64 mmol) in MeOH (20 mL) and the mixture was stirred at room temperature for overnight. The mixture was diluted with dichloromethane (60 mL), washed with aqueous ammonium chloride (saturated, 1×20 mL), dried (MgSO4), filtered and the solvent was evaporated under reduced pressure to give tert-butyl 5-(2-(4-fluorophenyl)-6-(N′-hydroxycarbamimidoyl)-1-oxo-1,2-dihydroisoquinolin-3-yl)pentanoate (200 mg, 0.441 mmol) as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290454B2
Source datasetuspto-grants-2016_03
ORD IDord-adc6e820905c4dde885de98843bed77f
Source noteuspto-grants-2016_03