C₂₃H₃₅N₃O₅

Base Information

Chemical Name:C₂₃H₃₅N₃O₅
CAS No.:914989-28-9
Molecular Formula:C₂₃H₃₅N₃O₅
Molecular Weight:433.548
Hs Code.:

C<sub>23</sub>H<sub>35</sub>N<sub>3</sub>O<sub>5</sub>

Synonyms:C₂₃H₃₅N₃O₅

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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 C₂₃H₃₅N₃O₅

Chemical Property:

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Technology Process of C₂₃H₃₅N₃O₅

There total 10 articles about C₂₃H₃₅N₃O₅ 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:

: 85838-94-4
N-Boc-1,2,3,6-tetrahydropyridine

: 914989-28-9
C₂₃H₃₅N₃O₅

Guidance literature:: Multi-step reaction with 5 steps

1.1: 92 percent / m-chloroperoxybenzoic acid / CH₂Cl₂ / 18 h / 20 °C

2.1: ethanol / 6 h / Heating

2.2: 27 percent / CHCl₃ / 6 h / 20 °C

3.1: 82 percent / pyridine*SO₃; Et₃N / dimethylsulfoxide / 3 h / 5 °C

4.1: 81 percent / NaHCO₃; HONH₂*HCl / ethanol; tetrahydrofuran / 1 h / 40 °C

5.1: TBAB; aq. NaOH / CH₂Cl₂ / 5 h / 20 °C

With sodium hydroxide; hydroxylamine hydrochloride; tetrabutylammomium bromide; sulfur trioxide pyridine complex; sodium hydrogencarbonate; triethylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; ethanol; dichloromethane; dimethyl sulfoxide;
DOI:10.1016/j.bmcl.2007.05.093

Reference yield:

: 914988-39-9
C₁₆H₂₉N₃O₅

: 100-39-0
benzyl bromide

: 914989-28-9
C₂₃H₃₅N₃O₅

Guidance literature:: With sodium hydroxide; tetrabutylammomium bromide; In dichloromethane; at 20 ℃; for 5h;
DOI:10.1016/j.bmcl.2007.05.093

Reference yield:

: 694-05-3
1,2,3,6-tetrahydropyridine

: 914989-28-9
C₂₃H₃₅N₃O₅

Guidance literature:: Multi-step reaction with 6 steps

1.1: CHCl₃ / 12 h / 20 °C

2.1: 92 percent / m-chloroperoxybenzoic acid / CH₂Cl₂ / 18 h / 20 °C

3.1: ethanol / 6 h / Heating

3.2: 27 percent / CHCl₃ / 6 h / 20 °C

4.1: 82 percent / pyridine*SO₃; Et₃N / dimethylsulfoxide / 3 h / 5 °C

5.1: 81 percent / NaHCO₃; HONH₂*HCl / ethanol; tetrahydrofuran / 1 h / 40 °C

6.1: TBAB; aq. NaOH / CH₂Cl₂ / 5 h / 20 °C

With sodium hydroxide; hydroxylamine hydrochloride; tetrabutylammomium bromide; sulfur trioxide pyridine complex; sodium hydrogencarbonate; triethylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; ethanol; dichloromethane; chloroform; dimethyl sulfoxide;
DOI:10.1016/j.bmcl.2007.05.093