HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1763016Erstellt: 25. Oktober 2026
Dimethylformamide → 9-Amino-7-chloro-3,4-dihydroacridin-1(2H)-one
https://huagongshe.com/reaction/1763016
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Benzonitrile, 2-((3-oxo-1-cyclohexen-1-yl)amino)- | HCID 184360 | — |
| Edukt | 5-Chloro-2-(3-oxocyclohexen-1-yl)amino-benzonitrile | HCID 14500186 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 9-Amino-7-chloro-3,4-dihydroacridin-1(2H)-one | HCID 13756057 | 4% |
Reaktionsschritte
In 5 liters of toluene were combined 200ml of dimethyl-formamide, 180.71 g of 5-chloro-2-(3-oxocyclohexen-1-yl)amino-benzonitrile hydrochloroide prepared in the same manner as the compounds of EXAMPLES 1 and 2, 176 g (2 eq) of milled K2CO3 and 3 g of cuprous chloride (CuCl). After 6 hours of reflux 3 g more of CuCl was added. After 12 hours of reflux 3 g more of CuCl was added. After overnight reflux the reaction mixture was evaporated and the residue extracted with dichloromethane via a Soxhlet extraction apparatus for 12 hours. The dichloromethane solution was evaporated to a solid. The solid was suspended in water and H2SO4 was added. The resultant salt which precipitated out was filtered and made basic with 10% NaOH. The solid was filtered and recrystallized twice from isopropanol/toluene to yield 6.84 g (4%) of a solid, melting point over 260° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04835275 |
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| Quelldatensatz | uspto-grants-1989_05 |
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| ORD ID | ord-a20a6eee3836462db3fe44818a0839af |
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| Quellennotiz | uspto-grants-1989_05 |
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