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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370723Generated: October 30, 2026

Sodium Hydroxide → Isoquinoline, 5-chloro-6-fluoro-

https://huagongshe.com/reaction/2370723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantChlorosuccinimideHCID 31398—
Reactant6-FluoroisoquinolineHCID 21889847—
SolventSulfuric AcidHCID 1118—
ProductIsoquinoline, 5-chloro-6-fluoro-HCID 5981826158.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

7.0 g (38.1 mmol) 6-Fluoroisoquinoline (5) were dissolved in 60 ml concentrated sulfuric acid. At 0° C. 10.18 g N-chlorosuccinimide were added. After 1 h another 5.2 g of N-chlorosuccinimide were added and the solution was warmed to 50° C. Two more portions of 5.2 g N-chlorosuccinimide were added successively and stirring was continued at 50° C. until the reaction was complete. The reaction mixture was cooled to room temperature, poured on ice and adjusted to pH 10 by addition of sodium hydroxide. The precipitate was filtered off, taken up in dichloromethane and washed with aqueous sodium hydroxide. The organic layer was dried over magnesium sulfate, evaporated and the crude product was purified by preparative HPLC to yield 4.04 g of the desired product as trifluoroacetate. Rt=0.97 min (Method #2). Detected mass: 182.0/184.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710228B2
Source datasetuspto-grants-2014_04
ORD IDord-8a7019924d6d4ff39903911833002782
Source noteuspto-grants-2014_04