Trifluoroacetic acid → 6-Chloro-7-(4-(6-(4-chlorophenyl)pyridin-2-ylcarbamoyl)phenoxy)chroman-4-carboxylic acid
반응식
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[O:12][C:13]1[CH:18]=[CH:17][C:16]([C:19](=[O:34])[NH:20][C:21]3[CH:26]=[CH:25][CH:24]=[C:23]([C:27]4[CH:32]=[CH:31][C:30]([Cl:33])=[CH:29][CH:28]=4)[N:22]=3)=[CH:15][CH:14]=1)[O:8][CH2:7][CH2:6][CH:5]2[C:35]([O:37]C(C)(C)C)=[O:36].FC(F)(F)C(O)=O>ClCCl>[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[O:12][C:13]1[CH:14]=[CH:15][C:16]([C:19](=[O:34])[NH:20][C:21]3[CH:26]=[CH:25][CH:24]=[C:23]([C:27]4[CH:32]=[CH:31][C:30]([Cl:33])=[CH:29][CH:28]=4)[N:22]=3)=[CH:17][CH:18]=1)[O:8][CH2:7][CH2:6][CH:5]2[C:35]([OH:37])=[O:36]참가 물질
4
실험 절차
Enantiomer 2 of tert-butyl 6-chloro-7-(4-(6-(4-chlorophenyl)pyridin-2-ylcarbamoyl)phenoxy)chroman-4-carboxylate (10 mg, 0.017 mmol) was diluted with dichloromethane (100 μL) followed by the addition of trifluoroacetic acid (100 μL). After stirring for 2 hours, the reaction was concentrated to yield Enantiomer 2 of 6-chloro-7-(4-(6-(4-chlorophenyl)pyridin-2-ylcarbamoyl)phenoxy)chroman-4-carboxylic acid (9.0 mg, 0.017 mmol, 99% yield). MS (apci, positive) m/z=535.1. 1H NMR (400 MHz, CDCl3) δ 9.03 (br s, 1H), 8.35 (d, 1H), 7.96 (d, 2H), 7.90-7.85 (m, 4H), 7.48-7.42 (m, 4H), 7.05 (d, 2H), 6.60 (s, 1H), 4.29-4.23 (m, 2H), 3.82 (t, 1H), 2.36 (dd, 1H), 2.19-2.10 (m, 1H).