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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 6-Fluoroisoquinoline | HCID 21889847 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | Isoquinoline, 5-chloro-6-fluoro- | HCID 59818261 | 58.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710228B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-8a7019924d6d4ff39903911833002782 |
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| Source note | uspto-grants-2014_04 |
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