Trifluoroacetic acid → HCID 9866355、化合物
反応式
C(OC(=O)[NH:7][C:8]1[CH:13]=[CH:12][C:11]([C:14]2[CH:19]=[CH:18][C:17]([F:20])=[CH:16][C:15]=2[O:21]COC)=[CH:10][C:9]=1[NH:25][C:26](=[O:41])[CH2:27][C:28]([C:30]1[CH:35]=[CH:34][CH:33]=[C:32]([N:36]2[CH:40]=[CH:39][N:38]=[CH:37]2)[CH:31]=1)=O)(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[F:20][C:17]1[CH:18]=[CH:19][C:14]([C:11]2[CH:12]=[CH:13][C:8]3[N:7]=[C:28]([C:30]4[CH:35]=[CH:34][CH:33]=[C:32]([N:36]5[CH:40]=[CH:39][N:38]=[CH:37]5)[CH:31]=4)[CH2:27][C:26](=[O:41])[NH:25][C:9]=3[CH:10]=2)=[C:15]([OH:21])[CH:16]=1参加物
4
実験手順
Prepared from {4′-fluoro-3-[3-(3-imidazol-1-yl-phenyl)-3-oxo-propionylamino]-2′-methoxymethoxy-biphenyl-4-yl}-carbamic acid tert.-butyl ester (Example K51) by treatment with TFA in CH2Cl2 according to the general procedure M. Obtained as a light yellow solid (13 mg).
出典と根拠
- ORDレコード
- ord-de049a9ba1484381bb4af0893466d2d0