Hydrazine → HCID 21254045, Verbindung
Reaktionsgleichung
[CH3:1][C:2]1[CH:3]=[C:4]([C:9]2[NH:10][C:11]3[C:16]([C:17]=2[CH2:18][CH2:19][N:20]2C(=O)C4C(=CC=CC=4)C2=O)=[CH:15][C:14]([OH:31])=[CH:13][CH:12]=3)[CH:5]=[C:6]([CH3:8])[CH:7]=1.NN>C(O)C.O1CCCC1>[NH2:20][CH2:19][CH2:18][C:17]1[C:16]2[C:11](=[CH:12][CH:13]=[C:14]([OH:31])[CH:15]=2)[NH:10][C:9]=1[C:4]1[CH:3]=[C:2]([CH3:1])[CH:7]=[C:6]([CH3:8])[CH:5]=1Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
To a solution of 2-[2-[2-(3,5-dimethylphenyl)-5-hydroxy-1H-indol-3-yl]ethyl]isoindole-1,3-dione (418 mg in a mixture of 7 mL ethanol and 7 mL tetrahydrofuran) was added 2.5 mL of 95% aqueous hydrazine and the reaction stirred at room temperature. After 12 hours the mixture was concentrated in vacuo and purified by flash chromatography on silica gel (methylene chloride:methanol:ammonium hydroxide, 89:11:1) to provide the title compound (228 mg).
Aufarbeitung
- concentrationAfter 12 hours the mixture was concentrated in vacuo
- custompurified by flash chromatography on silica gel (methylene chloride:methanol:ammonium hydroxide, 89:11:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-3e1c9d2647cc4d9591b98d05d00e2463
- Quelldatensatz
- uspto-grants-2001_03
- Patentnummer
- US06197975B1
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