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HRID 4835Erstellt: 24. Oktober 2026
Isopropanol → 2,3-Dihydro-4-methyl-2-[2-(4-morpholinyl)ethyl]-pyrido[3,2-f][1,4]oxazepin-5(4H)-one maleate
https://huagongshe.com/de/reaction/4835
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Isopropanol | HCID 3776 | — |
| Edukt | Morpholine | HCID 8083 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Maleic Acid | HCID 444266 | — |
| Edukt | 2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]oxazepin-5(4H)one hydrochloride | HCID 13726437 | — |
| Produkt | 2,3-Dihydro-4-methyl-2-[2-(4-morpholinyl)ethyl]-pyrido[3,2-f][1,4]oxazepin-5(4H)-one maleate | HCID 13726489 | — |
Reaktionsschritte
2-(2-Chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]oxazepin-5(4H)-one hydrochloride, 16 g (058 mole) was dissolved in morpholine (30 mL) and stirred overnight at room temperature. To the solution was added dilute sodium hydroxide solution (50 ml) and the resulting mixture extracted with chloroform (3×30 ml). The chloroform was removed on the rotary evaporator with aspiration. The residual morpholine was removed in vacuo at 50° C. (rotary evaporator). To the residual free base (15.5 g, 0.053 mole) was added isopropyl alcohol (1 liter) and maleic acid (9.24 g g, 0.080 mole). The mixture was heated to boiling and the clear solution cooled at 20° C. for several hours. The resulting crystals, 16 g (68.1%), were recrystallized from isopropyl alcohol, m.p. 163°-165° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04727152 |
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| Quelldatensatz | uspto-grants-1988_02 |
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| ORD ID | ord-86d68c4097fe4b1490aca906d3daf585 |
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| Quellennotiz | uspto-grants-1988_02 |
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