HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 349053Erstellt: 25. Oktober 2026
Carbon Dioxide → 1-[Butyl(methyl)amino]isoquinoline-7-carboxylic acid
https://huagongshe.com/reaction/349053
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Carbon Dioxide | HCID 280 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 7-bromo-N-butyl-N-methylisoquinolin-1-amine | HCID 21085997 | — |
| Edukt | CID 53628100 | HCID 178418400 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 1-[Butyl(methyl)amino]isoquinoline-7-carboxylic acid | HCID 21085178 | — |
Reaktionsschritte
To a −60° C. solution of 7-bromo-N-butyl-N-methylisoquinolin-1-amine (230 mg, 0.78 mmol) in diethyl ether was added sec-butyllithium (1.00 mL of a 1.3 M solution in cyclohexanes, 1.30 mmol). The solution was stirred at −60° C. for 20 min then excess dry ice (CO2) was added and the reaction mixture was allowed to warm to room temperature. The reaction mixture was then acidified with 1 N hydrochloric acid and extracted with ethyl acetate. The aqueous phase was concentrated under reduced pressure to yield a yellow oil. Purification by flash column chromatography (silica, 50:30:15:5 ethyl acetate/chloroform/methanol/ammonium hydroxide) provided 1-[butyl(methyl)amino]isoquinoline-7-carboxylic acid (90 mg): ESI MS m/z 259 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07176242B2 |
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| Quelldatensatz | uspto-grants-2007_02 |
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| ORD ID | ord-b3b11033f5154408a9c6a788d4ba66d5 |
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| Quellennotiz | uspto-grants-2007_02 |
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