HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 333990Erstellt: 25. Oktober 2026
Hydrochloric Acid → Isoquinoline-6-sulfonyl chloride
https://huagongshe.com/reaction/333990
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sulfite | HCID 1099 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 6-Aminoisoquinoline | HCID 588991 | — |
| Edukt | Sodium Bisulfite | HCID 23665763 | — |
| Edukt | Sodium Nitrite | HCID 23668193 | — |
| Katalysator | Cupric Chloride | HCID 24014 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | Isoquinoline-6-sulfonyl chloride | HCID 55280287 | — |
Reaktionsschritte
4.0 g of commercially available 6-aminoisoquinoline was suspended in 40 mL of concentrated hydrochloric acid (35%) with cooling at 0° C. To the suspension, 4.0 g of sodium nitrite was added in small portions, and the mixture was stirred for 30 minutes. This reaction solution was added dropwise at 0° C. to a mixed solution of 20 mL of acetic acid saturated with sulfite gas generated from sodium bisulfite and sulfuric acid, and 298 mg of copper chloride, and the mixture was stirred for 1 hour. The mixture was neutralized by the addition of a saturated aqueous solution of sodium bicarbonate, followed by extraction with dichloromethane (100 mL×2). The obtained organic layer was washed with saturated saline and then dried over anhydrous sodium sulfate. A dichloromethane solution obtained by filtration was used in the next reaction without being further purified because the compound of interest was unstable.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08883792B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-06d43ef930574f218e847d9d08bfe332 |
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| Quellennotiz | uspto-grants-2014_11 |
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