9-<2,3-anhydro-5-O-<(tert-butyl)diphenylsilyl>-β-D-ribofuranosyl>adenine

Base Information

Chemical Name:9-<2,3-anhydro-5-O-<(tert-butyl)diphenylsilyl>-β-D-ribofuranosyl>adenine
CAS No.:125084-70-0
Molecular Formula:C₂₆H₂₉N₅O₃Si
Molecular Weight:487.633
Hs Code.:

Synonyms:9-<2,3-anhydro-5-O-<(tert-butyl)diphenylsilyl>-β-D-ribofuranosyl>adenine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 9-<2,3-anhydro-5-O-<(tert-butyl)diphenylsilyl>-β-D-ribofuranosyl>adenine

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Technology Process of 9-<2,3-anhydro-5-O-<(tert-butyl)diphenylsilyl>-β-D-ribofuranosyl>adenine

There total 3 articles about 9-<2,3-anhydro-5-O-<(tert-butyl)diphenylsilyl>-β-D-ribofuranosyl>adenine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

: 2627-64-7
9-(2,3-anhydro-β-D-ribofuranosyl)adenine

: 58479-61-1
tert-butylchlorodiphenylsilane

: 125084-70-0
9-<2,3-anhydro-5-O-<(tert-butyl)diphenylsilyl>-β-D-ribofuranosyl>adenine

Guidance literature:: In pyridine; at 20 ℃; for 12h;
DOI:10.1021/jo010935d

Reference yield: 87.4%

: 557771-59-2
(2R,3S,4S,5R)-2-(6-amino-9H-purin-9-yl)-4-bromo-5-((tert-butyldiphenylsilyloxy)methyl)tetrahydrofuran-3-yl acetate

: 125084-70-0
9-<2,3-anhydro-5-O-<(tert-butyl)diphenylsilyl>-β-D-ribofuranosyl>adenine

: 125084-68-6
9-<3-bromo-5-O-<(tert-butyl)diphenylsilyl>-3-deoxy-β-D-xylofuranosyl>adenine

Guidance literature:: With ammonia; In methanol; at 4 ℃;
DOI:10.1002/hlca.200390069

Reference yield:

: 58-61-7
adenosine

: 125084-70-0
9-<2,3-anhydro-5-O-<(tert-butyl)diphenylsilyl>-β-D-ribofuranosyl>adenine

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) α-acetoxyisobutyryl bromide; 2.) Dowex 1x2 (OH^-) resin / 1.) MeCN/H2O, RT, 1 h; 2.) MeOH, RT, 15 min

2: 87 percent / pyridine / 16 h / Ambient temperature

With pyridine; Dowex 1x2 (OH^-) resin; acetoxyisobutyryl bromide;
DOI:10.1002/(SICI)1522-2675(19990407)82:4<597::AID-HLCA597>3.0.CO;2-V