Benzyl succinimido carbonate → Benzyl 2-methyl-4-(2,2,2-trifluoroethylamino)butan-2-ylcarbamate
반응식
[CH3:1][C:2]([NH2:12])([CH3:11])[CH2:3][CH2:4][NH:5][CH2:6][C:7]([F:10])([F:9])[F:8].[C:13](ON1C(=O)CCC1=O)([O:15][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)=[O:14]>C1COCC1>[CH3:11][C:2]([NH:12][C:13](=[O:14])[O:15][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)([CH2:3][CH2:4][NH:5][CH2:6][C:7]([F:8])([F:9])[F:10])[CH3:1]참가 물질
4
실험 절차
Crude 3-methyl-N1-(2,2,2-trifluoroethyl)butane-1,3-diamine (3.86 g, 21.0 mmol) was dissolved into THF (200 mL) and cooled in an ice bath. A THF (50 mL) solution of CbzOSu (5.22 g, 1 equiv, 21.0 mmol) was added to the reaction dropwise over 5 min. The reaction was left to stand in an ice chest for 16 h. The solvent was removed and the residue was taken up in a mixture of ethyl acetate (150 mL) and water (50 mL). The layers were separated and the organic layer washed with 1 M sodium carbonate (2×50 mL), 1 M HCl (50 mL) and brine (50 mL). The organic layer was dried over anhydrous MgSO4, filtered and concentrated to a pale yellow oil (6.15 g). The crude oil was purified on an ISCO purification system with gradient elution from 0-6% methanol in DCM. The desired fractions were collected and concentrated to give a pale yellow oil (4.57 g, yield: 68.5%). 1H NMR (CDCl3, 400 MHz): δ 1.33 (s, 6H), 1.75-1.83 (t, J=7.2, 2H), 2.74-2.85 (t, J=7.2, 2H) 3.10-3.18 (q, J=9.4, 2H), 5.04 (s, 2H), 7.27-7.38 (m, 5H). LRMS (ESI+) for C15H21F3N2O2 (318.2); Found: 319 (MH+).