5'-O-(TERT-BUTYLDIMETHYLSILYL)-5-IODO-2'-DEOXYCYTIDINE
5'-O-(TERT-BUTYLDIMETHYLSILYL)-5-IODO-2'-DEOXYCYTIDINE Basic information
- Product Name:
- 5'-O-(TERT-BUTYLDIMETHYLSILYL)-5-IODO-2'-DEOXYCYTIDINE
- Synonyms:
-
- 5'-O-tert-Butylmethylsilyl-2'-deoxy-5-iodocytidine
- 2'-Deoxy-5'-O-[(1,1-dimethylethyl)dimethylsilyl]-5-iodocytidine
- 4-amino-1-[(2R,4S,5R)-5-[[tert-butyl(dimethyl)silyl]oxymethyl]-4-hydroxyoxolan-2-yl]-5-iodopyrimidin-2-one
- 5'-O-TBDMS-5-Iodo-2'-DeoxyCytidine
- 4-Amino-1-((2R,4S,5R)-5-(((tert-butyldimethylsilyl)oxy)methyl)-4-hydroxytetrahydrofuran-2-yl)-5-iodopyrimidin-2(1H)-one
- 5-TBDMS-5-I-2-dC
- 5'-O-tert-Butyldimethylsilyl-2'-deoxy-5-iodocytidine
- 5′-O-TBS IODO DC
- CAS:
- 666848-11-9
- MF:
- C15H26IN3O4Si
- MW:
- 467.37
- Mol File:
- 666848-11-9.mol
5'-O-(TERT-BUTYLDIMETHYLSILYL)-5-IODO-2'-DEOXYCYTIDINE Chemical Properties
- Boiling point:
- 485.7±55.0 °C(Predicted)
- Density
- 1.58±0.1 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- pka
- 14.02±0.60(Predicted)
- Appearance
- White to off-white Solid
- InChI
- InChI=1S/C15H26IN3O4Si/c1-15(2,3)24(4,5)22-8-11-10(20)6-12(23-11)19-7-9(16)13(17)18-14(19)21/h7,10-12,20H,6,8H2,1-5H3,(H2,17,18,21)/t10-,11+,12+/m0/s1
- InChIKey
- GKUIXIRTAVPIGD-QJPTWQEYSA-N
- SMILES
- O([Si](C(C)(C)C)(C)C)C[C@H]1O[C@@H](N2C=C(I)C(N)=NC2=O)C[C@@H]1O
5'-O-(TERT-BUTYLDIMETHYLSILYL)-5-IODO-2'-DEOXYCYTIDINE Usage And Synthesis
Synthesis
611-53-0
666848-11-9
GENERAL STEPS: To a solution of 5-iodo-2'-deoxycytidine (2.2 g, 6.23 mmol) in anhydrous DMF (130 mL) was added imidazole (467 mg, 6.85 mmol). The reaction mixture was cooled to 0 °C and tert-butyldimethylsilyl chloride (TBDMSCl) (1.33 g, 6.85 mmol) was added slowly over 5 min. The reaction mixture was stirred at room temperature for 18 h and then concentrated under reduced pressure to remove volatiles. The residue was purified by fast column chromatography on silica gel with EtOAc:MeOH as eluent (95:5 to 90:10) to afford the target product 4-amino-1-((2R,4S,5R)-5-(((tert-butyldimethylsilyl)oxy)methyl)-4-hydroxytetrahydrofuran-2-yl)-5-iodopyrimidin-2(1H)-one (2.10 g, 72% yield) and unreacted feedstock (490 mg). The products were characterized as follows: 1H NMR (d6-DMSO) δ 0.11 (s, 3H, CH3), 0.12 (s, 3H, CH3), 0.89 (s, 9H, 3×CH3), 1.90 (ddd, J = 13.2, 7.7, 5.7 Hz, 1H, H-2'), 2.18 (ddd, J = 13.2, 5.7, 2.3 Hz, 1H, H-2'), 3.72 (ddd, J = 11.5, 3.6 Hz, 1H, H-5'), 3.80 (ddd, J = 11.5, 2.8 Hz, 1H, H-5'), 3.86-3.89 (m, 1H, H-4'), 4.14-4.18 (m, 1H, H-3'), 5.22 (ddd, J = 4.1 Hz, 1H, OH), 6.14-4.18 (m, 1H, H-3'), 5.22 (ddd, J = 4.1 Hz, 1H 1H, OH), 6.09 (dd, J = 7.8, 5.8 Hz, 1H, H-1'), 6.60 (br s, 1H, NH), 7.81 (br s, 1H, NH), 7.94 (s, 1H, H-6); MS (ES): m/z (%) (M + H)+ 468 (90%).
References
[1] Patent: EP2607369, 2015, B1. Location in patent: Paragraph 0183
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