C₂₄H₃₄N₆O₆

Base Information

Chemical Name:C₂₄H₃₄N₆O₆
CAS No.:1301627-73-5
Molecular Formula:C₂₄H₃₄N₆O₆
Molecular Weight:502.571
Hs Code.:

C<sub>24</sub>H<sub>34</sub>N<sub>6</sub>O<sub>6</sub>

Synonyms:C₂₄H₃₄N₆O₆

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Chemical Property of C₂₄H₃₄N₆O₆

Chemical Property:

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Technology Process of C₂₄H₃₄N₆O₆

There total 5 articles about C₂₄H₃₄N₆O₆ 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:

: 1204085-45-9
2-(2-azidoethoxy)ethanamine hydrochloride

: C₂₀H₂₆N₂O₆

: 1301627-73-5
C₂₄H₃₄N₆O₆

Guidance literature:: C₂₀H₂₆N₂O₆; With 4-methyl-morpholine; 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 0 ℃; for 0.0833333h; Inert atmosphere;

2-(2-azidoethoxy)ethanamine hydrochloride; In N,N-dimethyl-formamide; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/ol200861f

Reference yield:

: 949894-57-9
(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-(4-(prop-2-yn-1-yloxy)phenyl) propanoate

: 1301627-73-5
C₂₄H₃₄N₆O₆

Guidance literature:: Multi-step reaction with 4 steps

1.1: lithium hydroxide monohydrate / tetrahydrofuran; water / 0 °C / Inert atmosphere

1.2: pH 2 - 3 / Inert atmosphere

2.1: 4-methyl-morpholine; 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 0.08 h / 0 °C / Inert atmosphere

2.2: 0 - 20 °C / Inert atmosphere

3.1: lithium hydroxide monohydrate / tetrahydrofuran; water / 0 °C / Inert atmosphere

3.2: pH 2 - 3 / Inert atmosphere

4.1: 4-methyl-morpholine; 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 0.08 h / 0 °C / Inert atmosphere

4.2: 0 - 20 °C / Inert atmosphere

With 4-methyl-morpholine; 1-hydroxy-7-aza-benzotriazole; lithium hydroxide monohydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; water; N,N-dimethyl-formamide;
DOI:10.1021/ol200861f

Reference yield:

: 4326-36-7
(S)-N-(tert-butoxycarbonyl)tyrosine methyl ester

: 1301627-73-5
C₂₄H₃₄N₆O₆

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium carbonate; potassium iodide / acetone / 24 h / Inert atmosphere; Reflux

2.1: lithium hydroxide monohydrate / tetrahydrofuran; water / 0 °C / Inert atmosphere

2.2: pH 2 - 3 / Inert atmosphere

3.1: 4-methyl-morpholine; 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 0.08 h / 0 °C / Inert atmosphere

3.2: 0 - 20 °C / Inert atmosphere

4.1: lithium hydroxide monohydrate / tetrahydrofuran; water / 0 °C / Inert atmosphere

4.2: pH 2 - 3 / Inert atmosphere

5.1: 4-methyl-morpholine; 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 0.08 h / 0 °C / Inert atmosphere

5.2: 0 - 20 °C / Inert atmosphere

With 4-methyl-morpholine; 1-hydroxy-7-aza-benzotriazole; lithium hydroxide monohydrate; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; potassium iodide; In tetrahydrofuran; water; N,N-dimethyl-formamide; acetone;
DOI:10.1021/ol200861f