HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402572Generated: October 31, 2026
Sodium Hydroxide → Isoquinoline, 5-chloro-6-fluoro-
https://huagongshe.com/reaction/2402572
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) of 6-fluoroisoquinoline (3) were dissolved in 60 mL of concentrated sulfuric acid. At 0° C. 10.18 g of N-chloro succinimide were added. After 1 h another 5.2 g of N-chloro succiminide were added and the solution was heated to 50° C. Two more portions of 5.2 g N-chloro succinimide were added successively and stirring was continued at 50° C. until the reaction was complete. The reaction mixture was cooled to room temperature, was poured on ice and adjusted to pH 10 by addition of sodium hydroxide. The precipitate was filtered off, dissolved 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 5-chloro-6-fluoro-isoquinoline (7) as trifluoroacetate. Rt=0.97 min (Method A). Detected mass: 182.0/184.0 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08796458B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-e464f8bd750a4159b39fe44cb3774119 |
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| Source note | uspto-grants-2014_08 |
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