C₄₇H₆₁F₉N₅O₁₀S₂⁽¹⁺⁾

Base Information

Chemical Name:C₄₇H₆₁F₉N₅O₁₀S₂⁽¹⁺⁾
CAS No.:1643531-28-5
Molecular Formula:C₄₇H₆₁F₉N₅O₁₀S₂
Molecular Weight:1091.15
Hs Code.:

C<sub>47</sub>H<sub>61</sub>F<sub>9</sub>N<sub>5</sub>O<sub>10</sub>S<sub>2</sub><sup>(1+)</sup>

Synonyms:C₄₇H₆₁F₉N₅O₁₀S₂⁽¹⁺⁾

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Chemical Property of C₄₇H₆₁F₉N₅O₁₀S₂⁽¹⁺⁾

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Technology Process of C₄₇H₆₁F₉N₅O₁₀S₂⁽¹⁺⁾

There total 6 articles about C₄₇H₆₁F₉N₅O₁₀S₂⁽¹⁺⁾ 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: 55.0%

: 2BrH*C₁₀H₂₅N₃O₃S

: 1643531-25-2
C₃₇H₃₈F₉N₂O₈S⁽¹⁺⁾

: 1643531-28-5
C₄₇H₆₁F₉N₅O₁₀S₂⁽¹⁺⁾

Guidance literature:: C₃₇H₃₈F₉N₂O₈S⁽¹⁺⁾; With O-(N-succinimidyl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h; Cooling with ice;

2BrH*C₁₀H₂₅N₃O₃S; With sodium hydrogencarbonate; In N,N-dimethyl-formamide; at 0 ℃; for 2h;
DOI:10.1039/c4ob00456f

Reference yield:

: 1307863-97-3
C₂₉H₃₀N₂O₅

: 1643531-28-5
C₄₇H₆₁F₉N₅O₁₀S₂⁽¹⁺⁾

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / acetonitrile / 1 h / 20 °C

2.1: 2,6-di-tert-butyl-pyridine; 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate / 16 h / 155 °C / Sealed tube

3.1: hydrogenchloride / acetonitrile / 16 h / Reflux

4.1: O-(N-succinimidyl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.5 h / 20 °C / Cooling with ice

4.2: 2 h / 0 °C

With hydrogenchloride; 2,6-di-tert-butyl-pyridine; potassium carbonate; O-(N-succinimidyl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate; In N,N-dimethyl-formamide; acetonitrile;
DOI:10.1039/c4ob00456f

Reference yield:

: 1307863-96-2
C₂₄H₁₉NO₅

: 1643531-28-5
C₄₇H₆₁F₉N₅O₁₀S₂⁽¹⁺⁾

Guidance literature:: Multi-step reaction with 5 steps

2.1: potassium carbonate / acetonitrile / 1 h / 20 °C

3.1: 2,6-di-tert-butyl-pyridine; 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate / 16 h / 155 °C / Sealed tube

4.1: hydrogenchloride / acetonitrile / 16 h / Reflux

5.1: O-(N-succinimidyl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.5 h / 20 °C / Cooling with ice

5.2: 2 h / 0 °C

With hydrogenchloride; 2,6-di-tert-butyl-pyridine; potassium carbonate; O-(N-succinimidyl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate; In N,N-dimethyl-formamide; acetonitrile; 1.1: |Mitsunobu Displacement;
DOI:10.1039/c4ob00456f