Trifluoroacetic acid → HCID 67442611、化合物
反応式
[CH:1]1([NH:4][C:5](=[O:42])[NH:6][C:7]2[N:12]=[CH:11][C:10]([O:13][C:14]3[CH:19]=[CH:18][N:17]=[C:16]4[CH:20]=[C:21]([C:23]5[N:28]=[CH:27][C:26]([CH2:29][N:30]([CH2:38][CH2:39][O:40][CH3:41])C(=O)OC(C)(C)C)=[CH:25][CH:24]=5)[S:22][C:15]=34)=[CH:9][CH:8]=2)[CH2:3][CH2:2]1.C(O)(C(F)(F)F)=O>C(Cl)Cl>[CH:1]1([NH:4][C:5]([NH:6][C:7]2[CH:8]=[CH:9][C:10]([O:13][C:14]3[CH:19]=[CH:18][N:17]=[C:16]4[CH:20]=[C:21]([C:23]5[CH:24]=[CH:25][C:26]([CH2:29][NH:30][CH2:38][CH2:39][O:40][CH3:41])=[CH:27][N:28]=5)[S:22][C:15]=34)=[CH:11][N:12]=2)=[O:42])[CH2:2][CH2:3]1参加物
4
実験手順
A solution of 28 (754 mg, 1.27 mmol) and TFA (5 mL) in DCM (25 mL) was stirred at RT for 5.5 hr. The TFA was removed by co-evaporation with DCM, dissolved in a minimum of methanol, diluted with water, and the pH was adjusted to around 13 with 1N NaOH. The resulting sticky suspension was extracted with DCM in the presence of traces of methanol. The combined organic layer was dried over anhydrous magnesium sulfate, filtered, and concentrated. The residue was purified by Biotage (SiliaSep 40 g cartridge; 2% of ammonium hydroxide in MeOH/DCM: 1/99 to 10/90 over 20 CV) to produce a material that upon trituration with MeOH afforded the title compound 29 (360 mg, 0.734 mmol, 67% yield over 2 steps) as a white fluffy solid. 1H NMR (400 MHz, DMSO-d6) δ (ppm): 9.23 (bs, 1H), 8.56 (d, J=1.6 Hz, 1H), 8.51 (d, J=5.5 Hz, 1H), 8.31 (s, 1H), 8.27-8.20 (m, 2H), 7.89 (dd, J=8.2, 2.2 Hz, 1H), 7.79-7.72 (m, 2H), 7.66 (bd, J=9.0 Hz, 1H), 6.69 (d, J=5.5 Hz, 1H), 3.78 (s, 2H), 3.41 (t, J=5.9 Hz, 2H), 3.24 (s, 3H), 2.68-2.57 (m, 3H), 0.74-0.60 (m, 2H), 0.52-0.39 (m, 2H), one NH is missing. MS (m/z): 491.6 (M±H).