C([O:3][C:4]([C:6]1([NH:11][C:12]([CH:14]2[CH2:18][CH:17]([O:19][C:20]3[C:29]4[C:24](=[CH:25][C:26]([O:30][CH3:31])=[CH:27][CH:28]=4)[N:23]=[C:22]([C:32]4[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=4)[CH:21]=3)[CH2:16][NH:15]2)=[O:13])[CH2:8][CH:7]1[CH:9]=[CH2:10])=[O:5])C.[Li+].[OH-].CC(O)=O.C1(C)C=CC=CC=1>C1COCC1.CO>[CH3:31][O:30][C:26]1[CH:25]=[C:24]2[C:29]([C:20]([O:19][C@H:17]3[CH2:16][NH:15][C@H:14]([C:12]([NH:11][C@:6]4([C:4]([OH:5])=[O:3])[CH2:8][C@H:7]4[CH:9]=[CH2:10])=[O:13])[CH2:18]3)=[CH:21][C:22]([C:32]3[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=3)=[N:23]2)=[CH:28][CH:27]=1To a solution of compound 6 (0.067 mmol) in THF-MeOH 2:3 (2 ml) was added 1M LiOH 10 equiv. The solution was kept at 50° C. for 2.5 hrs. After cooling to RT, HOAc 20 eq. was added followed by toluene (2 ml) and then concentrated to dryness. The residue was taken up in DCM and filtered form the salts which gave the title compound (0.07 mmol). Purity >95% by HPLC M+H+ 474.
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