COC1C=CC(C[N:8]2[N:14]=[C:13]([N:15]3[CH2:20][CH2:19][C:18]4[N:21]=[C:22]([C:24]5[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=5)[O:23][C:17]=4[CH2:16]3)[CH:12]3[CH:10]([CH2:11]3)[C:9]2=[O:30])=CC=1.C1(OC)C(=CC=CC=1)OC.C(O)(C(F)(F)F)=O.C(=O)([O-])[O-].[Na+].[Na+]>>[C:24]1([C:22]2[O:23][C:17]3[CH2:16][N:15]([C:13]4[CH:12]5[CH:10]([CH2:11]5)[C:9](=[O:30])[NH:8][N:14]=4)[CH2:20][CH2:19][C:18]=3[N:21]=2)[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1320 mg (0.75 mmol) 3-(4-methoxy-benzyl)-5-(2-phenyl-6,7-dihydro-4H-oxazolo[5,4-c]pyridin-5-yl)-3,4-diaza-bicyclo[4.1.0]hept-4-en-2-one, 1 ml (7.84 mmol) Veratrol and 6 ml TFA are heated to 100° C. in a pressure vessel for 24 h. The cooled mixture is combined with sat. sodium carbonate solution and extracted with DCM, the org. phase is concentrated by rotary evaporation i. V. and the residue is purified by silica gel (eluant: DCM/methanol).
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