C₅₄H₆₁ClN₄O₁₈

Base Information

Chemical Name:C₅₄H₆₁ClN₄O₁₈
CAS No.:949000-18-4
Molecular Formula:C₅₄H₆₁ClN₄O₁₈
Molecular Weight:1089.55
Hs Code.:

C<sub>54</sub>H<sub>61</sub>ClN<sub>4</sub>O<sub>18</sub>

Synonyms:C₅₄H₆₁ClN₄O₁₈

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Chemical Property of C₅₄H₆₁ClN₄O₁₈

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Technology Process of C₅₄H₆₁ClN₄O₁₈

There total 6 articles about C₅₄H₆₁ClN₄O₁₈ 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%

: C₅₄H₅₉ClN₄O₁₈

: 949000-18-4
C₅₄H₆₁ClN₄O₁₈

Guidance literature:: With borane-THF; copper(II) bis(trifluoromethanesulfonate); In tetrahydrofuran; dichloromethane; at 20 ℃; for 0.5h;
DOI:10.1021/jo070669p

Reference yield:

: 948999-99-3
C₂₅H₃₀O₇S

: 949000-18-4
C₅₄H₆₁ClN₄O₁₈

Guidance literature:: Multi-step reaction with 3 steps

1: 93 percent / 2,6-di-tert-butyl-4-methylpyridine; AgOTf; molecular sieves 4 Angstroem / dioxane; toluene / 0 - 20 °C

2: 65 percent / N-(phenylthio)-ε-caprolactam; Tf2O; 4 Angstroem molecular sieves / CH2Cl2 / 1 h / 4 - 20 °C

3: 76 percent / BH₃*THF; Cu(OTf)2 / CH₂Cl₂; tetrahydrofuran / 0.5 h / 20 °C

With N-(phenylthio)-ε-caprolactam; 2,6-di-tert-butyl-4-methylpyridine; borane-THF; trifluoromethylsulfonic anhydride; 4 A molecular sieve; silver trifluoromethanesulfonate; copper(II) bis(trifluoromethanesulfonate); In tetrahydrofuran; 1,4-dioxane; dichloromethane; toluene;
DOI:10.1021/jo070669p

Reference yield:

: C₂₅H₂₈O₇S

: 949000-18-4
C₅₄H₆₁ClN₄O₁₈

Guidance literature:: Multi-step reaction with 4 steps

1: 84 percent / HCl; NaBH₃CN; molecular sieves 3 Angstroem / dioxane; tetrahydrofuran / 0.5 h / 0 °C

2: 93 percent / 2,6-di-tert-butyl-4-methylpyridine; AgOTf; molecular sieves 4 Angstroem / dioxane; toluene / 0 - 20 °C

3: 65 percent / N-(phenylthio)-ε-caprolactam; Tf2O; 4 Angstroem molecular sieves / CH2Cl2 / 1 h / 4 - 20 °C

4: 76 percent / BH₃*THF; Cu(OTf)2 / CH₂Cl₂; tetrahydrofuran / 0.5 h / 20 °C

With hydrogenchloride; N-(phenylthio)-ε-caprolactam; 2,6-di-tert-butyl-4-methylpyridine; borane-THF; trifluoromethylsulfonic anhydride; 3 A molecular sieve; 4 A molecular sieve; silver trifluoromethanesulfonate; copper(II) bis(trifluoromethanesulfonate); sodium cyanoborohydride; In tetrahydrofuran; 1,4-dioxane; dichloromethane; toluene;
DOI:10.1021/jo070669p