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ChemicalBook CAS DataBase List N2-isobutyryl-5'-O-(4,4'-dimethoxytrityl)-3'-O-tert-butyldimethylsilyl guanosine
81256-89-5

N2-isobutyryl-5'-O-(4,4'-dimethoxytrityl)-3'-O-tert-butyldimethylsilyl guanosine synthesis

4synthesis methods
tert-Butyldimethylsilyl chloride

18162-48-6

5'-O-DMTr-N2-isobutyrylguanosine

81246-83-5

N2-isobutyryl-5'-O-(4,4'-dimethoxytrityl)-3'-O-tert-butyldimethylsilyl guanosine

81256-89-5

Synthesis of 3'-DMTBS-5'-O-(4,4') tetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)isobutyramide from tert-butyldimethylchlorosilane and N-(9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(1-hydroxy-2,2-bis(4-methoxyphenyl)-2-phenylethyl)-6-oxo-6,9-dihydro-1H-purin-2-yl)isobutyramide. -dimethoxytrityl)-N2-isobutyryl acylcytidine in the following general steps: to a solution of compound HLH (23.9 g, 36.450 mmol, 1.00 eq.) in N,N-dimethylformamide (120 mL) was added tert-butyldimethylchlorosilane (8.24 g, 54.675 mmol, 1.50 eq.) and 1H-imidazole ( 6.204 g, 91.124 mmol, 2.50 equiv). The reaction mixture was stirred at 25 °C overnight. After completion of the reaction, the reaction was quenched with methanol (5 mL) and the mixture was concentrated to give the residue. The residue was purified by preparative HPLC (mobile phase: water (containing 0.225% formic acid)-acetonitrile gradient elution) to afford compound LII (6.7 g, 24% yield) as a yellow solid.LC-MS analysis showed ESI-MS m/z 770.3 [M+H]+.

18162-48-6 Synthesis
tert-Butyldimethylsilyl chloride

18162-48-6
679 suppliers
$9.00/5g

81279-39-2 Synthesis
N2-Isobutyryl-2''-O-(tert-butyldimethylsilyl)-5''-O-(4,4''-dimethoxytrityl)-gu

81279-39-2
95 suppliers
$27.00/250mg

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Yield:81256-89-5 34% ,81279-39-2 63%

Reaction Conditions:

in dichloromethane at 20;

References:

Wexselblatt, Ezequiel;Katzhendler, Jehoshua;Saleem-Batcha, Raspudin;Hansen, Guido;Hilgenfeld, Rolf;Glaser, Gad;Vidavski, Roee R. [Bioorganic and Medicinal Chemistry,2010,vol. 18,# 12,p. 4485 - 4497] Location in patent:scheme or table

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