C₂₂H₂₆Cl₂N₃O₁₁P

Base Information

Chemical Name:C₂₂H₂₆Cl₂N₃O₁₁P
CAS No.:1564286-07-2
Molecular Formula:C₂₂H₂₆Cl₂N₃O₁₁P
Molecular Weight:610.342
Hs Code.:

C<sub>22</sub>H<sub>26</sub>Cl<sub>2</sub>N<sub>3</sub>O<sub>11</sub>P

Synonyms:C₂₂H₂₆Cl₂N₃O₁₁P

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Chemical Property of C₂₂H₂₆Cl₂N₃O₁₁P

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Technology Process of C₂₂H₂₆Cl₂N₃O₁₁P

There total 5 articles about C₂₂H₂₆Cl₂N₃O₁₁P 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: 76.0%

: 1564286-18-5
C₂₆H₃₆Cl₂N₃O₁₂P

: 1564286-07-2
C₂₂H₂₆Cl₂N₃O₁₁P

Guidance literature:: With pyridinium p-toluenesulfonate; In water; acetone; for 5h; Reflux;
DOI:10.1021/ja411733s

Reference yield:

: 1564286-12-9
C₂₅H₃₃N₄O₈P

: 1564286-07-2
C₂₂H₂₆Cl₂N₃O₁₁P

Guidance literature:: Multi-step reaction with 4 steps

1.1: 5-(ethylthio)-1H-tetrazole / acetonitrile / 1 h / 25 °C / Inert atmosphere

1.2: 0.33 h / Inert atmosphere

2.1: hydrazine / tetrahydrofuran; water / 0.08 h / 25 °C

3.1: acetic acid / dimethyl sulfoxide / 37 °C

4.1: pyridinium p-toluenesulfonate / water; acetone / 5 h / Reflux

With pyridinium p-toluenesulfonate; acetic acid; 5-(ethylthio)-1H-tetrazole; hydrazine; In tetrahydrofuran; water; dimethyl sulfoxide; acetone; acetonitrile;
DOI:10.1021/ja411733s

Reference yield:

: C₂₆H₃₄N₃O₁₂P

: 1564286-07-2
C₂₂H₂₆Cl₂N₃O₁₁P

Guidance literature:: Multi-step reaction with 3 steps

1: hydrazine / tetrahydrofuran; water / 0.08 h / 25 °C

2: acetic acid / dimethyl sulfoxide / 37 °C

3: pyridinium p-toluenesulfonate / water; acetone / 5 h / Reflux

With pyridinium p-toluenesulfonate; acetic acid; hydrazine; In tetrahydrofuran; water; dimethyl sulfoxide; acetone;
DOI:10.1021/ja411733s