HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1735139Erstellt: 25. Oktober 2026
Sodium hydride → 2-(2-oxopyrrolidin-1-yl)-N-(3-methyl-5,6,7,8-tetrahydrothieno[2,3-b]quinolin-4-yl)acetamide
https://huagongshe.com/reaction/1735139
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Methyl 2-oxo-1-pyrrolidineacetate | HCID 108835 | — |
| Edukt | 4-Amino-3-methyl-5,6,7,8-tetrahydrothieno[2,3-b]quinoline | HCID 15225118 | — |
| Lösungsmittel | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Produkt | 2-(2-oxopyrrolidin-1-yl)-N-(3-methyl-5,6,7,8-tetrahydrothieno[2,3-b]quinolin-4-yl)acetamide | HCID 15385071 | — |
Reaktionsschritte
Into a suspension of 1.26 g of sodium hydride (60% content) in 15 ml of N-methylpyrrolidone, was added 3.28 g of 4-amino-3-methyl -5,6,7,8-tetrahydrothieno[2,3-b]quinoline at room temperature. The mixture was heated to 50° C. and stirred for 40 minutes. Thereafter, 4.72 g of methyl 2-oxo-1-pyrrolidine acetate was added dropwise to the mixture at 50° C. over a period of 30 minutes. After the stirring at 50° C. for 20 minutes, the mixture was cooled to 15° C. and poured into 130 ml aqueous solution containing 13.5 g of ammonium chloride.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05536728 |
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| Quelldatensatz | uspto-grants-1996_07 |
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| ORD ID | ord-c7bd126c74b34fce87ad06e4d24f7d7b |
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| Quellennotiz | uspto-grants-1996_07 |
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