Reaktionsgleichung
[C:1](OC(=O)C)(=[O:3])C.[NH2:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[C:21]3[CH:22]=[C:23]4[O:28][CH2:27][O:26][C:24]4=[CH:25][C:20]=3[CH2:19][CH:18]([CH3:29])[NH:17][N:16]=2)=[CH:11][CH:10]=1.[CH:30](O)=[O:31]>>[CH:1]([NH:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[C:21]3[CH:22]=[C:23]4[O:28][CH2:27][O:26][C:24]4=[CH:25][C:20]=3[CH2:19][CH:18]([CH3:29])[N:17]([CH:30]=[O:31])[N:16]=2)=[CH:11][CH:10]=1)=[O:3]Komponenten
4
Reaktionsbedingungen
- Temperatur
- 25 °C
Versuchsvorschrift
To 6.0 ml (0.104 mol) of acetic anhydride 3.0 ml (0.08 mol) of 100% formic acid were added dropwise at 0° C. during 5 minutes while constant stirring. The stirring was continued at 50° C. for 15 minutes. Thereafter 1 g (3.3 mmol) of 1-(4-aminophenyl)-4-methyl-7,8-methylenedioxy-3,4-dihydro-5H-2,3-benzodiazepine was added to the thus-prepared mixed anhydride. The reaction mixture was stirred at 25° C. for 1.5 hours, then poured into ice-water, the precipitate formed was filtered, washed with 4×5 ml of distilled water and dried at 80° C. to give 0.80 g of raw product. After crystallization from 3 ml of ethyl acetate 0.65 g (56.2%) of the aimed product was obtained, m.p.: 193°-195° C.
Aufarbeitung
- customthe precipitate formed
- filtrationwas filtered
- washwashed with 4×5 ml of distilled water
- customdried at 80° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-a8e6e1550e614f54a803090487433043
- Quelldatensatz
- uspto-grants-1997_06
- Patentnummer
- US05639751
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