HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2236881Erstellt: 26. Oktober 2026
Hydrochloric Acid → 4-aminomethyl-1-phenyl-1H-pyridin-2-one
https://huagongshe.com/reaction/2236881
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Tert-butyl (2-oxo-1-phenyl-1,2-dihydropyridin-4-ylmethyl)-carbamate | HCID 42625677 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 4-aminomethyl-1-phenyl-1H-pyridin-2-one | HCID 42625679 | — |
Reaktionsschritte
Tert-butyl (2-oxo-1-phenyl-1,2-dihydropyridin-4-ylmethyl)-carbamate (83 mg, 0.28 mmol) is treated with 4N hydrogen chloride in dioxane in order to remove the Boc protecting group. The hydrochloride salt of 4-aminomethyl-1-phenyl-1H-pyridin-2-one, obtained after concentration of the reaction mixture, is dissolved in N,N-dimethylformamide (5 mL) and is coupled to (4E)-6-iodo-4-(methoxymethylene)isoquinoline-1,3(2H,4H)-dione (92 mg, 0.28 mmol) in the presence of triethylamine (200 μL). After one hour, the reaction mixture is concentrated under reduced pressure and purified by flash silica gel chromatography (methanol/chloroform) to provide (4Z)-6-iodo-4-({[(2-oxo-1-phenyl-1,2dihydropyridin-4-yl)methyl]amino}methylene)isoquinoline-1,3(2H,4H)-dione as a pale yellow solid (8.8 mg, 6.3%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07713994B2 |
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| Quelldatensatz | uspto-grants-2010_05 |
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| ORD ID | ord-82f64a456fe64485ab95f97483ea8b69 |
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| Quellennotiz | uspto-grants-2010_05 |
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