Trifluoroacetic acid → HCID 86749246、化合物
反応式
C(OC([NH:8][C@@H:9]([CH2:19][S:20]C(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[CH2:10][N:11]1[CH2:18][CH2:17][CH2:16][C@H:12]1[C:13]([OH:15])=[O:14])=O)(C)(C)C.[Cl:40][C:41]1[C:49]([Cl:50])=[CH:48][CH:47]=[CH:46][C:42]=1[C:43]([NH2:45])=[O:44].C(C(O)=O)(F)(F)F.C([SiH](CC)CC)C>C(Cl)Cl>[NH2:8][C@@H:9]([CH2:19][SH:20])[CH2:10][N:11]1[CH2:18][CH2:17][CH2:16][C@H:12]1[C:13]([OH:15])=[O:14].[Cl:40][C:41]1[C:49]([Cl:50])=[CH:48][CH:47]=[CH:46][C:42]=1[C:43]([NH2:45])=[O:44]参加物
5
実験手順
N-[2(R)-t-Butoxycarbonylamino-3-triphenylmethylmercaptopropyl]-L-proline-2,3-dichlorobenzamide (0.097 g, 0.14 mmol) was dissolved in CH2Cl2(3 mL), CF3CO2H (1 mL) at ambient temperature, treated with triethylsilane (0.088 mL, 0.55 mmol) and stirred for 1 h. The reaction mixture was triturated with 0.1% TFA in H2O, filtered, concentrated and chromatographed by RP-HPLC and lyophilized. The residue was dissolved in MeOH (1 mL), treated with concd HCl, concentrated and triturated with Et2O to provide the title compound as the his hydrochloride salt. 1H NMR (CD3OD) δ 7.50 (d, 1H, J=6 Hz), 7.27-7.4 (m, 2H),4.60 (ABq, 2H), 4.25-4.7 (m, 1H), 3.3-3.9 (m, 5H), 2.99 (d, 2H, J=5 Hz), 2.5-2.7 (m, 1H), 2.0-2.3 (m, 3H).