반응식
[OH:1][C:2]([CH2:4][CH2:5][CH2:6][CH2:7][C@H:8]1[C@@H:16]2[C@@H:11]([NH:12][C:13]([NH:15]2)=[O:14])[CH2:10][S:9]1)=[O:3].[I:17][CH2:18][CH2:19][CH2:20]O.CC1C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[I:17][CH2:18][CH2:19][CH2:20][O:3][C:2](=[O:1])[CH2:4][CH2:5][CH2:6][CH2:7][CH:8]1[CH:16]2[NH:15][C:13](=[O:14])[NH:12][CH:11]2[CH2:10][S:9]1참가 물질
실험 절차
A solution of biotin (125 mg, 0.5 mmol), 3-iodo-1-propanol (150 μL, 1.6 mmol) and TsOH (10 mg, 0.05 mmol) in PhMe (50 mL)) was heated under reflux and Ar for 3 d in a Dean-Stark apparatus. After cooling down to ambient temperature, the mixture was filtered and the solvent distilled off under reduced pressure. The residue was dissolved in CH2Cl2 (30 mL) and washed with H2O (5 mL). The organic phase was dried (MgSO4) and concentrated under reduced pressure to yield 4 (75 mg, 36%) as a white solid. FABMS: m/z=413 [M+H]+; 1H-NMR (400 MHz, CDCl3): δ=1.40-1.45 (2H, m), 1.61-1.75 (4H, m), 2.10-2.16 (2H, m), 2.30 (2H, t, 7 Hz), 2.79 (1H, d, 13 Hz), 2.88 (1H, dd, 5 and 13 Hz), 3.15-3.18 (1H, m), 3.22 (2H, t, 7 Hz), 4.13 (2H, t, 6 Hz), 4.42-4.45 (1H, m), 4.61-4.65 (1H, m), 7.22 (1H, d, 8 Hz); 7.72 (1H, d, 8 Hz); 13C-NMR (100 MHz, CDCl3): δ=25.0, 28.4, 28.8, 32.6, 34.2, 40.5, 55.8, 61.8, 63.6, 64.4, 164.5, 173.9.
후처리
- temperatureunder reflux
- filtrationthe mixture was filtered
- distillationthe solvent distilled off under reduced pressure
- dissolutionThe residue was dissolved in CH2Cl2 (30 mL)
- washwashed with H2O (5 mL)
- dry with materialThe organic phase was dried (MgSO4)
- concentrationconcentrated under reduced pressure
출처 및 근거
- ORD 기록
- ord-e6b6d367fcd14702857bb6d468633735
- 출처 데이터셋
- uspto-grants-2012_06
- 특허 번호
- US08198099B2
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