HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1257117Erstellt: 27. Oktober 2026
HCID 178471673, Verbindung → 7-Fluoroisoquinolin-3-amine
https://huagongshe.com/reaction/1257117
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | HCID 178471673 | HCID 178471673 | — |
| Lösungsmittel | Sulfuric Acid | HCID 1118 | — |
| Produkt | 7-Fluoroisoquinolin-3-amine | HCID 23321140 | 2,5% |
Reaktionsschritte
The crude 2,2-diethoxy-N-(3-fluorobenzyl)acetimidamide (22 g) was added dropwise to conc. sulfuric acid (200 mL) at 20˜25° C. with stirring. The mixture was stirred at room temperature for 48 hours. Then this mixture was quenched with ice (1 Kg), and a 12 N NaOH solution (400 mL) was added. The final pH of 9˜10 was reached. The suspension was extracted with CH2Cl2 (5×2 L). The organic layers were combined, washed with brine (500 mL), dried over anhydrous Na2SO4, filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (EtOAc/Hexane=1/1) and afforded the title compound (330 mg, 2.5% yield based on m-fluorobenzylamine) as a yellow solid. 1H NMR (300 MHz, CDCl3): 9.17 (s, 1H), 8.66 (s, 1H), 8.01˜8.07 (m, 2H), 7.68 (dd, J=2.4, and 8.7 Hz, 1H), 7.58 (m, 1H); MS: m/z 163.1 (M+H+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08461339B2 |
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| Quelldatensatz | uspto-grants-2013_06 |
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| ORD ID | ord-4a9083c6b428441393955558a80cce26 |
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| Quellennotiz | uspto-grants-2013_06 |
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