HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23619Erstellt: 23. Oktober 2026
Synephrine → N-(4-chlorobenzyl)-2-{[[2-hydroxy-2-(4-hydroxyphenyl)ethyl](methyl)amino]methyl}-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide
https://huagongshe.com/de/reaction/23619
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Synephrine | HCID 7172 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | N-(4-chlorobenzyl)-2-(chloromethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide | HCID 22574363 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-(4-chlorobenzyl)-2-{[[2-hydroxy-2-(4-hydroxyphenyl)ethyl](methyl)amino]methyl}-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide | HCID 10289450 | 77,6% |
Reaktionsschritte
A mixture of N-(4-chlorobenzyl)-2-(chloromethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide (48 mg, 0.12 mmol), synephrine (Aldrich, 30 mg, 0.18 mmol) and diisopropylethylamine (31 μL, 0.18 mmol) in dry DMF (2.0 mL) was heated to 60° C., becoming a solution. The reaction was stirred for 3 hours at that temperature. After cooling to room temperature, the solution was diluted with water (5 mL). The resulting milky suspension was stirred vigorously for 30 minutes, and then left standing overnight at room temp. The mixture was filtered, and the collected solid was washed with water and dried in vacuo, leaving a white solid. Recrystallization from acetonitrile (10 mL, dissolved with warming and then cooled to 0° C. overnight) gave the title compound (49 mg) as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06852731B2 |
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| Quelldatensatz | uspto-grants-2005_02 |
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| ORD ID | ord-43f95aaa0dac428ca9a4a8e01f7df808 |
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| Quellennotiz | uspto-grants-2005_02 |
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