C₃₅H₄₈N₄O₆

Base Information Edit

Chemical Name:C₃₅H₄₈N₄O₆
CAS No.:1384352-91-3
Molecular Formula:C₃₅H₄₈N₄O₆
Molecular Weight:620.789
Hs Code.:
Mol file:1384352-91-3.mol

C<sub>35</sub>H<sub>48</sub>N<sub>4</sub>O<sub>6</sub>

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Chemical Property of C₃₅H₄₈N₄O₆ Edit

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Technology Process of C₃₅H₄₈N₄O₆

There total 3 articles about C₃₅H₄₈N₄O₆ 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:

: 774214-21-0
[3-cyclohexyl-6-(methoxycarbonyl)-2-(4-methoxyphenyl)-1H-indol-1-yl]acetic acid

: 263162-13-6
tert-butyl N-[2-[(2-aminoethyl)(methyl)amino]ethyl]carbamate

: 1384352-91-3
C₃₅H₄₈N₄O₆

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In dichloromethane; at 20 ℃;
DOI:10.1016/j.bmcl.2012.03.097

Reference yield:

: 494799-19-8
methyl 2-bromo-3-cyclohexyl-1H-indole-6-carboxylate

: 1384352-91-3
C₃₅H₄₈N₄O₆

Guidance literature:: Multi-step reaction with 4 steps

1: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate; lithium chloride / ethanol; water; toluene / 12 h / 80 °C

2: sodium hydride / N,N-dimethyl-formamide / 20 °C

3: trifluoroacetic acid / dichloromethane / 20 °C

4: N-ethyl-N,N-diisopropylamine; HATU / dichloromethane / 20 °C

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium hydride; sodium carbonate; N-ethyl-N,N-diisopropylamine; HATU; trifluoroacetic acid; lithium chloride; In ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene; 1: Suzuki-Miyaura reaction;
DOI:10.1016/j.bmcl.2012.03.097

Reference yield:

: 848485-50-7
methyl 3-cyclohexyl-2-(4-methoxyphenyl)-1H-indole-6-carboxylate

: 1384352-91-3
C₃₅H₄₈N₄O₆

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydride / N,N-dimethyl-formamide / 20 °C

2: trifluoroacetic acid / dichloromethane / 20 °C

3: N-ethyl-N,N-diisopropylamine; HATU / dichloromethane / 20 °C

With sodium hydride; N-ethyl-N,N-diisopropylamine; HATU; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2012.03.097