C₅₆H₆₉N₆O₁₅P

Base Information

Chemical Name:C₅₆H₆₉N₆O₁₅P
CAS No.:1146622-45-8
Molecular Formula:C₅₆H₆₉N₆O₁₅P
Molecular Weight:1097.17
Hs Code.:

C<sub>56</sub>H<sub>69</sub>N<sub>6</sub>O<sub>15</sub>P

Synonyms:C₅₆H₆₉N₆O₁₅P

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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 C₅₆H₆₉N₆O₁₅P

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Technology Process of C₅₆H₆₉N₆O₁₅P

There total 12 articles about C₅₆H₆₉N₆O₁₅P 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: 88.0%

: 1146622-43-6
C₄₇H₅₂N₄O₁₄

: 124482-92-4,89992-70-1
2-cyanoethyl-N,N-(diisopropylamino)chlorophosphine

: 1146622-45-8
C₅₆H₆₉N₆O₁₅P

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 0.5h; Inert atmosphere;
DOI:10.1039/c0cc02028a

Reference yield:

: 50-89-5,28854-96-8,3545-96-8,50-88-4
thymidine

: 1146622-45-8
C₅₆H₆₉N₆O₁₅P

Guidance literature:: Multi-step reaction with 8 steps

1: pyridine / 20 °C

2: 1H-imidazole / N,N-dimethyl-formamide / 20 °C

3: trifluoroacetic acid / methanol; dichloromethane / 4 h / 0 °C

4: pyridine / 20 °C

5: caesium carbonate / N,N-dimethyl-formamide / 0.5 h / 20 °C

6: 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 0.27 h

7: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.17 h / 20 °C

8: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.5 h / 20 °C / Inert atmosphere

With pyridine; 1H-imidazole; tetrabutyl ammonium fluoride; caesium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1039/c0cc02028a

Reference yield:

: 1146622-39-0
C₂₀H₃₃BrN₂O₆Si

: 1146622-45-8
C₅₆H₆₉N₆O₁₅P

Guidance literature:: Multi-step reaction with 3 steps

1: 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 0.27 h

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.17 h / 20 °C

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.5 h / 20 °C / Inert atmosphere

With tetrabutyl ammonium fluoride; 1,8-diazabicyclo[5.4.0]undec-7-ene; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1039/c0cc02028a