C₂₆H₂₅N₃O₇S

Base Information

Chemical Name:C₂₆H₂₅N₃O₇S
CAS No.:1234347-61-5
Molecular Formula:C₂₆H₂₅N₃O₇S
Molecular Weight:523.566
Hs Code.:

C<sub>26</sub>H<sub>25</sub>N<sub>3</sub>O<sub>7</sub>S

Synonyms:C₂₆H₂₅N₃O₇S

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Chemical Property of C₂₆H₂₅N₃O₇S

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Technology Process of C₂₆H₂₅N₃O₇S

There total 3 articles about C₂₆H₂₅N₃O₇S 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: 51.0%

: 5174-26-5
N₄-benzoyl-2'-deoxycytidine-5'-tosylate

: 106-96-7
propargyl bromide

: 1234347-61-5
C₂₆H₂₅N₃O₇S

Guidance literature:: N₄-benzoyl-2'-deoxycytidine-5'-tosylate; With sodium hydride; In tetrahydrofuran; at 40 ℃; for 0.0333333h; Microwave irradiation;

propargyl bromide; In tetrahydrofuran; at 40 ℃; for 0.1h; Microwave irradiation;
DOI:10.1080/15257771003708579

Reference yield:

: 951-77-9
2'-Deoxycytidine

: 1234347-61-5
C₂₆H₂₅N₃O₇S

Guidance literature:: Multi-step reaction with 3 steps

1.1: pyridine; chloro-trimethyl-silane

2.1: pyridine / 3 h / 0 °C / Inert atmosphere

3.1: sodium hydride / tetrahydrofuran / 0.03 h / 40 °C / Microwave irradiation

3.2: 0.1 h / 40 °C / Microwave irradiation

With pyridine; chloro-trimethyl-silane; sodium hydride; In tetrahydrofuran;
DOI:10.1080/15257771003708579

Reference yield:

: 98-88-4
benzoyl chloride

: 1234347-61-5
C₂₆H₂₅N₃O₇S

Guidance literature:: Multi-step reaction with 3 steps

1.1: pyridine; chloro-trimethyl-silane

2.1: pyridine / 3 h / 0 °C / Inert atmosphere

3.1: sodium hydride / tetrahydrofuran / 0.03 h / 40 °C / Microwave irradiation

3.2: 0.1 h / 40 °C / Microwave irradiation

With pyridine; chloro-trimethyl-silane; sodium hydride; In tetrahydrofuran;
DOI:10.1080/15257771003708579