C₄₂H₅₀N₄O₁₀

Base Information

Chemical Name:C₄₂H₅₀N₄O₁₀
CAS No.:1460306-70-0
Molecular Formula:C₄₂H₅₀N₄O₁₀
Molecular Weight:770.88
Hs Code.:

C<sub>42</sub>H<sub>50</sub>N<sub>4</sub>O<sub>10</sub>

Synonyms:C₄₂H₅₀N₄O₁₀

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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 C₄₂H₅₀N₄O₁₀

Chemical Property:

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Technology Process of C₄₂H₅₀N₄O₁₀

There total 6 articles about C₄₂H₅₀N₄O₁₀ 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: 80.0%

: 1460306-69-7
C₂₇H₃₂N₂O₇

: 1460306-59-5
(R)-allyl 4-amino-2-(benzyloxycarbonylamino)butanoate toluene-4-sulfonate

: 1460306-70-0
C₄₂H₅₀N₄O₁₀

Guidance literature:: With 1-hydroxy-7-aza-benzotriazole; N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 15h;

Reference yield:

: 1251836-88-0
methyl 3’-hydroxybiphenyl-2-carboxylate

: 1460306-70-0
C₄₂H₅₀N₄O₁₀

Guidance literature:: Multi-step reaction with 3 steps

1: triphenylphosphine; 1,1'-azodicarbonyl-dipiperidine / chloroform / 15 h / 0 - 20 °C

2: methanol; lithium hydroxide / tetrahydrofuran / 4 h / 65 °C

3: N-ethyl-N,N-diisopropylamine; HATU; 1-hydroxy-7-aza-benzotriazole / N,N-dimethyl-formamide / 15 h / 0 - 20 °C

With methanol; 1-hydroxy-7-aza-benzotriazole; N-ethyl-N,N-diisopropylamine; triphenylphosphine; HATU; lithium hydroxide; 1,1'-azodicarbonyl-dipiperidine; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide;

Reference yield:

: 92379-10-7
3’-hydroxybiphenyl-2-carboxylic acid

: 1460306-70-0
C₄₂H₅₀N₄O₁₀

Guidance literature:: Multi-step reaction with 4 steps

1: thionyl chloride / 4.17 h / 0 °C / Reflux

2: triphenylphosphine; 1,1'-azodicarbonyl-dipiperidine / chloroform / 15 h / 0 - 20 °C

3: methanol; lithium hydroxide / tetrahydrofuran / 4 h / 65 °C

4: N-ethyl-N,N-diisopropylamine; HATU; 1-hydroxy-7-aza-benzotriazole / N,N-dimethyl-formamide / 15 h / 0 - 20 °C

With methanol; thionyl chloride; 1-hydroxy-7-aza-benzotriazole; N-ethyl-N,N-diisopropylamine; triphenylphosphine; HATU; lithium hydroxide; 1,1'-azodicarbonyl-dipiperidine; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide;