Indan-5-amine → N-(Indan-5-yl)-2-(4-trifluoromethyl-phenyl)-nicotinamide hydrochloride

Reaktionsgleichung

C1(S(N[CH:11]2[CH2:19][C:18]3[C:13](=[CH:14][CH:15]=[C:16]([NH:20][C:21]([C:23]4[C:24]([C:29]5[CH:34]=[CH:33][C:32]([C:35]([F:38])([F:37])[F:36])=[CH:31][CH:30]=5)=C[CH:26]=[CH:27][CH:28]=4)=[O:22])[CH:17]=3)[CH2:12]2)(=O)=O)C=CC=CC=1.FC(F)(F)C1C=CC(C2[N:55]=CC=CC=2C([Cl:51])=O)=CC=1.NC1C=C2C(=CC=1)CCC2>>[ClH:51].[CH2:12]1[C:13]2[C:18](=[CH:17][C:16]([NH:20][C:21](=[O:22])[C:23]3[CH:28]=[CH:27][CH:26]=[N:55][C:24]=3[C:29]3[CH:34]=[CH:33][C:32]([C:35]([F:38])([F:36])[F:37])=[CH:31][CH:30]=3)=[CH:15][CH:14]=2)[CH2:19][CH2:11]1

Komponenten

Edukt 3

HCID 90496Indan-5-amine

HCID 98933624''-Trifluoromethyl-biphenyl-2-carboxylic acid (2-benzenesulfonylamino-indan-5-yl)-amide

HCID 212533632-(4-Trifluoromethyl-phenyl)-nicotinoyl chloride

Produkt 1

HCID 21253373N-(Indan-5-yl)-2-(4-trifluoromethyl-phenyl)-nicotinamide hydrochloride

Versuchsvorschrift

The title compound is prepared in a manner similar to that described for the title E compound of Example 1 using 2-(4-trifluoromethyl-phenyl)-nicotinoyl chloride (2.228 mmol) and 5-aminoindan (0.296 g, 2.228 mmol) to give the product as the free base. The hydrochloride salt is prepared by bubbling HCl(g) through an ethyl acetate solution of the free base and trituation of the salt with diethyl ether; mp 190-205° C. MS (ES+) m/z 383 (M+1).