HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 441241Erstellt: 25. Oktober 2026
Methanol → 1-{4-[2-(4-Methylphenyl)benzoylamino]benzoyl}-1,2,3,4-tetrahydroquinoline
https://huagongshe.com/reaction/441241
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Methanol | HCID 887 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | (4-aminophenyl)(3,4-dihydroquinolin-1(2H)-yl)methanone | HCID 2984117 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 1-{4-[2-(4-Methylphenyl)benzoylamino]benzoyl}-1,2,3,4-tetrahydroquinoline | HCID 10503544 | — |
Reaktionsschritte
To a solution of 2-(4-methylphenyl)benzoic acid (140 mg) in dichloromethane (5 ml) were added oxalyl chloride (133 mg) and a few drop of N,N-dimethylformamide and the solution was stirred at ambient temperature for 2 hours. Dichloromethane was evaporated in vacuo to give an acid chloride as an oil and the oil was added to a mixture of 1-(4-aminobenzoyl)-1,2,3,4-tetrahydroquinoline (166 mg) and triethylamine (0.14 ml) in dichloromethane (20 ml). The mixture was stirred at ambient temperature for 2 hours, washed successively with diluted hydrogen chloride, water and brine and dried over magnesium sulfate. The solvent was evaporated in vacuo to give an oil and the oil was subjected to silica gel column (30 g, 1% methanol in chloroform) to give 1-{4-[2-(4-methylphenyl)benzoylamino]benzoyl}-1,2,3,4-tetrahydroquinoline (202 mg) as an amorphous solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05521170 |
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| Quelldatensatz | uspto-grants-1996_05 |
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| ORD ID | ord-f4e7c6fdea184ac1af3418aa2524b819 |
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| Quellennotiz | uspto-grants-1996_05 |
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