C₂₁H₂₅N₃O₇

Base Information

Chemical Name:C₂₁H₂₅N₃O₇
CAS No.:1207737-64-1
Molecular Formula:C₂₁H₂₅N₃O₇
Molecular Weight:431.445
Hs Code.:

C<sub>21</sub>H<sub>25</sub>N<sub>3</sub>O<sub>7</sub>

Synonyms:C₂₁H₂₅N₃O₇

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Chemical Property of C₂₁H₂₅N₃O₇

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Technology Process of C₂₁H₂₅N₃O₇

There total 3 articles about C₂₁H₂₅N₃O₇ 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: 82.0%

: 1207737-91-4
C₁₈H₂₃NO₇

: 7288-28-0
2,4-bis(trimethylsiloxy)-5-methylpyrimidine

: 1207737-64-1
C₂₁H₂₅N₃O₇

Guidance literature:: C₁₈H₂₃NO₇; 2,4-bis(trimethylsiloxy)-5-methylpyrimidine; In 1,2-dichloro-ethane; for 1h; Inert atmosphere; Reflux;

With trimethylsilyl trifluoromethanesulfonate; In 1,2-dichloro-ethane; at -78 ℃; for 2h; optical yield given as %de; diastereoselective reaction;
DOI:10.1016/j.tetlet.2009.09.006

Reference yield: 36.0%

: 1207737-85-6
C₁₇H₂₃NO₆

: 7288-28-0
2,4-bis(trimethylsiloxy)-5-methylpyrimidine

: 1207737-64-1
C₂₁H₂₅N₃O₇

Guidance literature:: C₁₇H₂₃NO₆; 2,4-bis(trimethylsiloxy)-5-methylpyrimidine; In 1,2-dichloro-ethane; for 1h; Inert atmosphere; Reflux;

With trimethylsilyl trifluoromethanesulfonate; In 1,2-dichloro-ethane; at -78 ℃; for 72h; optical yield given as %de; diastereoselective reaction;
DOI:10.1016/j.tetlet.2009.09.006

Reference yield:

: 1207737-85-6
C₁₇H₂₃NO₆

: 7288-28-0
2,4-bis(trimethylsiloxy)-5-methylpyrimidine

: 1207737-64-1
C₂₁H₂₅N₃O₇

: C₂₁H₂₅N₃O₇

Guidance literature:: C₁₇H₂₃NO₆; 2,4-bis(trimethylsiloxy)-5-methylpyrimidine; In 1,2-dichloro-ethane; for 1h; Inert atmosphere; Reflux;

With trimethylsilyl trifluoromethanesulfonate; In 1,2-dichloro-ethane; at 0 - 20 ℃; optical yield given as %de; diastereoselective reaction;
DOI:10.1016/j.tetlet.2009.09.006