HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 10553Erstellt: 25. Oktober 2026
Sodium Bicarbonate → N-(tert-butoxycarbonyl)-N'-(4-chloro-5-isoquinolyl)-1,4-cyclohexanediamine
https://huagongshe.com/reaction/10553
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 4-Chloroisoquinolin-5-amine | HCID 21979937 | — |
| Edukt | Tert-butyl 4-oxo-1-aminocyclohexylcarboxylate | HCID 21979990 | — |
| Katalysator | Titanium isopropoxide | HCID 11026 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-(tert-butoxycarbonyl)-N'-(4-chloro-5-isoquinolyl)-1,4-cyclohexanediamine | HCID 21979991 | — |
Reaktionsschritte
According to the method of Example 103, Step A, a mixture of Intermediate 90 (100 mg), tert-butyl 4-oxo-1-aminocyclohexylcarboxylate (270 mg), titanium tetraisopropoxide (0.34 ml) and dichloromethane (7 ml) was stirred at room temperature for 120 hours. The reaction mixture was added with sodium borohydride (94 mg) and methanol (1 ml) and stirred for 1.5 hours with ice cooling. The reaction mixture was added with saturated aqueous sodium hydrogencarbonate (10 ml) with ice cooling and then extracted twice with ethyl acetate (15 ml for each time). The organic layer was dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:1) to obtain the title compound (40.4 mg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07094789B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-2183330ad69d4daf8b0bf3debc9cee84 |
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| Quellennotiz | uspto-grants-2006_08 |
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