반응 #1994284

ord-12bf2652954840aa9503c8fdf7260ae9

반응 방정식

CC(C)(C)[Si](C)(C)Cl
tert-butyldimethylsilyl chloride
Nc1nc(=O)n([C@H]2C[C@H](O)[C@@H](CO)O2)cc1I
5-iodo-2′-deoxycytidine
c1c[nH]cn1
imidazole
CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](n2cc(I)c(N)nc2=O)C[C@@H]1O
expected product ( 39 )
수율 72.1%
CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](n2cc(I)c(N)nc2=O)C[C@@H]1O
5′-O-(tert-Butyldimethylsilyl)-5-iodo-2′-deoxycytidine
수율 72.1%

용매

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타the volatiles were evaporated under reduced pressure
  2. 2
    기타the residue purified by flash chromatography on silica gel with EtOAc:MeOH (95:5 to 90:10)

실험 절차

To a solution of 5-iodo-2′-deoxycytidine (2.2 g, 6.23 mmol) in DMF (130 ml) was added imidazole (467 mg, 6.85 mmol). The mixture was cooled at 0° C. and tert-butyldimethylsilyl chloride (TBDMSCl) (1.33 g, 6.85 mmol) added over 5 minutes. After 18 h at room temperature, the volatiles were evaporated under reduced pressure and the residue purified by flash chromatography on silica gel with EtOAc:MeOH (95:5 to 90:10) to give the expected product (39) (2.10 g, 72%) together with unreacted starting material (490 mg). 1H NMR (d6 DMSO) δ 0.11 (s, 3H, CH3), 0.12 (s, 3H, CH3), 0.89 (s, 9H, 3CH3), 1.90 (ddd, J=13.2, 7.7 and 5.7 Hz, 1H, 2.18 (ddd, J=13.2, 5.7 and 2.3 Hz, 1H, HH-2′), 3.72 (dd, J=11.5, 3.6 Hz, 1H, HH-5′), 3.80 (dd, J=11.5, 2.8 Hz, 1H, HH-5′), 3.86-3.89 (m, 1H, H-4′), 4.14-4.18 (m, 1H, H-3′), 5.22 (1H, d, J=4.1 Hz, OH), 6.09 (1H, dd, J=7.8, 5.8 Hz, H-1′), 6.60 (br s, 1H, NHH), 7.81 (br s, 1H, NRH), 7.94 (s, 1H, H-6); MS (ES): m/z (%) (M+H) 468 (90%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08597881B2uspto-grants-2013_12