Benzyl Alcohol → HCID 11599369、化合物
反応式
[CH2:1](OC1C=C(CC(O)=O)C=C(C2C=CC(C(F)(F)F)=CC=2)C=1)[C:2]1C=CC=C[CH:3]=1.[N:29]1([S:34]([C:37]2[CH:64]=[CH:63][C:40]([CH2:41][O:42][C:43]3[CH:44]=[C:45]([CH2:59][C:60]([OH:62])=[O:61])[CH:46]=[C:47]([C:49]4[CH:54]=[CH:53][C:52]([C:55]([F:58])([F:57])[F:56])=[CH:51][CH:50]=4)[CH:48]=3)=[CH:39][CH:38]=2)(=[O:36])=[O:35])[CH2:33][CH2:32][CH2:31][CH2:30]1.C(O)C1C=CC=CC=1.N1(S(C2C=CC(CO)=CC=2)(=O)=O)CCCC1>>[N:29]1([S:34]([C:37]2[CH:38]=[CH:39][C:40]([CH2:41][O:42][C:43]3[CH:44]=[C:45]([CH:59]([CH2:1][CH2:2][CH3:3])[C:60]([OH:62])=[O:61])[CH:46]=[C:47]([C:49]4[CH:54]=[CH:53][C:52]([C:55]([F:57])([F:58])[F:56])=[CH:51][CH:50]=4)[CH:48]=3)=[CH:63][CH:64]=2)(=[O:35])=[O:36])[CH2:33][CH2:32][CH2:31][CH2:30]1参加物
5
実験手順
Procedure as for example 110 replacing (5-benzyloxy-4′-trifluoromethyl-biphenyl-3-yl)-acetic acid with 5-[4-(pyrrolidine-1-sulfonyl)-benzyloxy]-4′-trifluoromethyl-biphenyl-3-yl-acetic acid, itself made according to the procedure of example 9 replacing benzyl alcohol with 4-(pyrrolidine-1-sulfonyl)-benzyl alcohol, afforded 2-{5-[4-(pyrrolidine-1-sulfonyl)-benzyloxy]-4′-trifluoromethyl-biphenyl-3-yl}-pentanoic acid, LC method B, retention time 12.6 min.