2-Aminoanthraquinone → 1-Aminoanthraquinone

HRID 64622

Reaktionsgleichung

Reaktionsgleichung von HRID 64622
[CH:1]1[CH:6]=[C:5]2[C:7]([C:9]3[CH:16]=[CH:15][C:14](N)=[CH:13][C:10]=3[C:11](=[O:12])[C:4]2=[CH:3][CH:2]=1)=[O:8].[NH2:18]C1C2C(=O)C3C(=CC=CC=3)C(=O)C=2C(N)=CC=1.NC1C2C(=O)C3C(=C(N)C=CC=3)C(=O)C=2C=CC=1.NC1C2C(=O)C3C(=CC=CC=3)C(=O)C=2C(NC(=O)C)=CC=1.NC1C2C(=O)C3C(=CC=CC=3)C(=O)C=2C(NC(=O)C2C=CC=CC=2)=CC=1.NC1C2C(=O)C3C(=C(NC(=O)C)C=CC=3)C(=O)C=2C=CC=1.NC1C2C(=O)C3C(=C(NC(=O)C4C=CC=CC=4)C=CC=3)C(=O)C=2C=CC=1.NC1C2C(=O)C3C(=CC=CC=3)C(=O)C=2C([N+]([O-])=O)=CC=1.NC1C2C(=O)C3C(=C([N+]([O-])=O)C=CC=3)C(=O)C=2C=CC=1.NC1C2C(=O)C3C(=CC=CC=3)C(=O)C=2C(Br)=CC=1.NC1C2C(=O)C3C(=CC=CC=3)C(=O)C=2C(NC)=CC=1.NC1C2C(=O)C3C(=CC=CC=3)C(=O)C=2C(NC2C=CC=CC=2)=CC=1>>[CH:1]1[CH:6]=[C:5]2[C:7]([C:9]3[CH:16]=[CH:15][CH:14]=[C:13]([NH2:18])[C:10]=3[C:11](=[O:12])[C:4]2=[CH:3][CH:2]=1)=[O:8]

Komponenten

13

Edukt 12

HCID 83412-AminoanthraquinoneHCID 85131,5-DiaminoanthraquinoneHCID 14650Disperse Violet 4HCID 20419Solvent Blue 68HCID 31420Disperse Violet 1HCID 66479Corinth flourHCID 67011Benzamide, N-(5-amino-9,10-dihydro-9,10-dioxo-1-anthracenyl)-HCID 80953N-(4-Amino-9,10-dihydro-9,10-dioxo-1-anthryl)acetamideHCID 2369001-Amino-5-nitroanthraquinoneHCID 2369091-Amino-5-acetylamino-anthraquinoneHCID 6273261-Amino-4-bromoanthraquinoneHCID 31272301-Amino-4-nitroanthracene-9,10-dione

Produkt 1

HCID 67101-Aminoanthraquinone

Versuchsvorschrift

β-aminoanthraquinone; 1,4diaminoanthraquinone; 1,5-diaminoanthraquinone; 1-amino-4-acetylaminoanthraquinone; 1-amino-4-benzoylamino anthraquinone; 1-amino-5-acetylamino-anthraquinone; 1-amino-5-benzoylamino-anthraquinone; 1-amino-4-nitro-anthraquinone; 1-amino-5-nitro-anthraquinone; 1-amino-4-bromo-anthraquinone; 1-amino-4-methylamino-anthraquinone; 1-amino-4-phenylamino-anthraquinone.

Quellen und Nachweise

ORD-Eintrag
ord-b5013e4747644e309bf4a162d75b04f1
Quelldatensatz
uspto-grants-1986_09
Patentnummer
US04609404

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