5'-O-levulinyl-N⁴-[O-(4,4'-dimethoxytrityloxy)hexyl]-5-methyl-2'-deoxycytidine

Base Information

Chemical Name:5'-O-levulinyl-N⁴-[O-(4,4'-dimethoxytrityloxy)hexyl]-5-methyl-2'-deoxycytidine
CAS No.:942223-85-0
Molecular Formula:C₄₂H₅₁N₃O₉
Molecular Weight:741.882
Hs Code.:

5'-O-levulinyl-N<sup>4</sup>-[O-(4,4'-dimethoxytrityloxy)hexyl]-5-methyl-2'-deoxycytidine

Synonyms:5'-O-levulinyl-N⁴-[O-(4,4'-dimethoxytrityloxy)hexyl]-5-methyl-2'-deoxycytidine

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Chemical Property of 5'-O-levulinyl-N⁴-[O-(4,4'-dimethoxytrityloxy)hexyl]-5-methyl-2'-deoxycytidine

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Technology Process of 5'-O-levulinyl-N⁴-[O-(4,4'-dimethoxytrityloxy)hexyl]-5-methyl-2'-deoxycytidine

There total 6 articles about 5'-O-levulinyl-N⁴-[O-(4,4'-dimethoxytrityloxy)hexyl]-5-methyl-2'-deoxycytidine 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:

: 942223-82-7
4-(1,2,4-triazol-1-yl)-5'-O-levulinyl-3'-O-tert-butyldimethylsilylthymidine

: 942223-85-0
5'-O-levulinyl-N⁴-[O-(4,4'-dimethoxytrityloxy)hexyl]-5-methyl-2'-deoxycytidine

Guidance literature:: Multi-step reaction with 3 steps

1: 88 percent / acetonitrile / 3 h / 20 °C

2: 80 percent / (N,N-dimethylamino)pyridine / pyridine / 20 °C

3: 98 percent / acetic acid; tetrabutylammoniun fluoride / tetrahydrofuran / 7 h / 20 °C

With dmap; tetrabutyl ammonium fluoride; acetic acid; In tetrahydrofuran; pyridine; acetonitrile;
DOI:10.1002/chem.200601473

Reference yield:

: 942223-83-8
5'-O-levulinyl-3'-O-tert-butyldimethylsilyl-N⁴-(6-hydroxyhexyl)-5-methyl-2'-deoxycytidine

: 942223-85-0
5'-O-levulinyl-N⁴-[O-(4,4'-dimethoxytrityloxy)hexyl]-5-methyl-2'-deoxycytidine

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / (N,N-dimethylamino)pyridine / pyridine / 20 °C

2: 98 percent / acetic acid; tetrabutylammoniun fluoride / tetrahydrofuran / 7 h / 20 °C

With dmap; tetrabutyl ammonium fluoride; acetic acid; In tetrahydrofuran; pyridine;
DOI:10.1002/chem.200601473

Reference yield:

: 942223-81-6
5'-O-levulinyl-3'-O-tert-butyldimethylsilylthymidine

: 942223-85-0
5'-O-levulinyl-N⁴-[O-(4,4'-dimethoxytrityloxy)hexyl]-5-methyl-2'-deoxycytidine

Guidance literature:: Multi-step reaction with 4 steps

1.1: POCl₃; Et₃N / acetonitrile / 0.75 h / 0 °C

1.2: 100 percent / acetonitrile / 1 h / 20 °C

2.1: 88 percent / acetonitrile / 3 h / 20 °C

3.1: 80 percent / (N,N-dimethylamino)pyridine / pyridine / 20 °C

4.1: 98 percent / acetic acid; tetrabutylammoniun fluoride / tetrahydrofuran / 7 h / 20 °C

With dmap; tetrabutyl ammonium fluoride; acetic acid; triethylamine; trichlorophosphate; In tetrahydrofuran; pyridine; acetonitrile;
DOI:10.1002/chem.200601473