Reaktion #53784

ord-0c92b7ab11774c20ab29507f5b0b0831

Reaktionsgleichung

COc1ccc(-c2cc3ccccc3[nH]2)cc1N
product
COc1ccc(-c2cc3ccccc3[nH]2)cc1N
5-(1H-Indol-2-yl)-2-methoxy-phenylamine
COc1ccc(-c2cc3ccccc3[nH]2)cc1N
5-(1H-indol-2-yl)-2-methoxy-phenylamine
NS(=O)(=O)c1ccc(N=C=S)cc1
4-isothiocyanatobenzene sulfonamide
→
COc1ccc(-c2cc3ccccc3[nH]2)cc1NC(=S)Nc1ccc(S(N)(=O)=O)cc1
product
COc1ccc(-c2cc3ccccc3[nH]2)cc1NC(=S)Nc1ccc(S(N)(=O)=O)cc1
4-{3-[5-(1H-Indol-2-yl)-2-methoxy-phenyl]-thioureido}-benzenesulfonamide

Edukte

COc1ccc(-c2cc3ccccc3[nH]2)cc1N
product
COc1ccc(-c2cc3ccccc3[nH]2)cc1N
5-(1H-Indol-2-yl)-2-methoxy-phenylamine
COc1ccc(-c2cc3ccccc3[nH]2)cc1N
5-(1H-indol-2-yl)-2-methoxy-phenylamine
NS(=O)(=O)c1ccc(N=C=S)cc1
4-isothiocyanatobenzene sulfonamide

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

The product from Example 1, Step B, 5-(1H-indol-2-yl)-2-methoxy-phenylamine (0.12 g, 0.1 mmol) was reacted with 4-isothiocyanatobenzene sulfonamide (0.108 g, 0.1 mmol) according to the procedure for Example 2 to give the product (0.14 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06858739B2uspto-grants-2005_02