C₃₇H₅₄N₆O₁₁

Base Information

Chemical Name:C₃₇H₅₄N₆O₁₁
CAS No.:1579275-64-1
Molecular Formula:C₃₇H₅₄N₆O₁₁
Molecular Weight:758.869
Hs Code.:

C<sub>37</sub>H<sub>54</sub>N<sub>6</sub>O<sub>11</sub>

Synonyms:C₃₇H₅₄N₆O₁₁

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Chemical Property of C₃₇H₅₄N₆O₁₁

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Technology Process of C₃₇H₅₄N₆O₁₁

There total 7 articles about C₃₇H₅₄N₆O₁₁ 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: 84.0%

: 1579275-60-7
C₄₆H₇₄N₆O₁₁Si

: 1579275-64-1
C₃₇H₅₄N₆O₁₁

Guidance literature:: With triethylamine tris(hydrogen fluoride); In acetonitrile; at 50 ℃; for 24h; Inert atmosphere;
DOI:10.1021/jo500039d

Reference yield:

: 1515605-77-2
(S)-5-azido-2-triisopropylsilyloxy-1-pentanol

: 1579275-64-1
C₃₇H₅₄N₆O₁₁

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine; sulfur trioxide pyridine complex / dimethyl sulfoxide / 0.5 h / 20 °C / Inert atmosphere

2: triethylphosphine / tetrahydrofuran; toluene / 30 h / 20 °C / Inert atmosphere

3: toluene / 48 h / 70 °C / Inert atmosphere

4: triethylamine tris(hydrogen fluoride) / acetonitrile / 24 h / 50 °C / Inert atmosphere

With sulfur trioxide pyridine complex; triethylamine tris(hydrogen fluoride); triethylamine; triethylphosphine; In tetrahydrofuran; dimethyl sulfoxide; toluene; acetonitrile; 2: |Staudinger Azide Reduction / 3: |Ugi Condensation;
DOI:10.1021/jo500039d

Reference yield:

: C₁₇H₂₄N₂O₆

: 1579275-64-1
C₃₇H₅₄N₆O₁₁

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydrogencarbonate / N,N-dimethyl-formamide / 24 h / 20 °C / Inert atmosphere

2: toluene / 48 h / 70 °C / Inert atmosphere

3: triethylamine tris(hydrogen fluoride) / acetonitrile / 24 h / 50 °C / Inert atmosphere

With sodium hydrogencarbonate; triethylamine tris(hydrogen fluoride); In N,N-dimethyl-formamide; toluene; acetonitrile; 2: |Ugi Condensation;
DOI:10.1021/jo500039d