Methyl 6-(benzenesulphonylmethyl)-2-(3-t-butoxycarbonylaminopropoxy)-3-(furan-3-yl)benzoate → 6-(Benzenesulphonylmethyl)-2-(3-t-butoxycarbonylaminopropoxy)-3-(furan-3-yl)benzoic acid
反応式
C1(S(CC2C(C(O)=O)=C(OCCNC(OC(C)(C)C)=O)C(C3C=COC=3)=CC=2)(=O)=O)C=CC=CC=1.[C:36]1([S:42]([CH2:45][C:46]2[C:51]([C:52]([O:54]C)=[O:53])=[C:50]([O:56][CH2:57][CH2:58][CH2:59][NH:60][C:61]([O:63][C:64]([CH3:67])([CH3:66])[CH3:65])=[O:62])[C:49]([C:68]3[CH:72]=[CH:71][O:70][CH:69]=3)=[CH:48][CH:47]=2)(=[O:44])=[O:43])[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=1>>[C:36]1([S:42]([CH2:45][C:46]2[C:51]([C:52]([OH:54])=[O:53])=[C:50]([O:56][CH2:57][CH2:58][CH2:59][NH:60][C:61]([O:63][C:64]([CH3:65])([CH3:66])[CH3:67])=[O:62])[C:49]([C:68]3[CH:72]=[CH:71][O:70][CH:69]=3)=[CH:48][CH:47]=2)(=[O:44])=[O:43])[CH:37]=[CH:38][CH:39]=[CH:40][CH:41]=1参加物
3
反応物 2
生成物 1
実験手順
Prepared by proceeding in a similar manner to Intermediate 6, starting from methyl 6-(benzenesulphonylmethyl)-2-(3-t-butoxycarbonylaminopropoxy)-3-(furan-3-yl)benzoate (Intermediate 109).