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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77389Generated: October 25, 2026

Water → 7-bromo-3-(3-chlorophenyl)-2-methylisoquinolin-1(2H)-one

https://huagongshe.com/reaction/77389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl-4-nitrobenzenesulfonateHCID 22582—
ReactantSodium hydrideHCID 24758—
Reactant7-bromo-3-(3-chlorophenyl)isoquinolin-1(2H)-oneHCID 69928893—
SolventTetrahydrofuranHCID 8028—
Product7-bromo-3-(3-chlorophenyl)-2-methylisoquinolin-1(2H)-oneHCID 6992854850.2%

Reaction Steps

7-Bromo-3-(3-chlorophenyl)isoquinolin-1(2H)-one (Intermediate 23A) (0.1 g, 0.299 mmol) was dissolved in THF (4 mL), under an atmosphere of nitrogen. Sodium hydride (0.018 g, 0.448 mmol) was added and reaction stirred for 30 minutes. The reaction was then cooled using an ice bath and methyl 4-nitrobenzenesulfonate (0.065 g, 0.299 mmol) was added. The reaction was allowed to warm to room temperature and left to stir overnight. Water was added to the reaction mixture and extracted with EtOAC (×2). The organics were combined and washed with brine, dried (MgSO4) filtered and concentrated under reduced pressure. The mixture was purified on silica (25 g column on Isolera 4) eluting with 0-10% methanol in dichloromethane to afford 7-bromo-3-(3-chlorophenyl)-2-methylisoquinolin-1(2H)-one (51 mg, 0.15 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841289B2
Source datasetuspto-grants-2014_09
ORD IDord-d964deca7655450c9db475cc20959061
Source noteuspto-grants-2014_09