C₂₄H₃₈N₂O₅

Base Information

Chemical Name:C₂₄H₃₈N₂O₅
CAS No.:1220904-24-4
Molecular Formula:C₂₄H₃₈N₂O₅
Molecular Weight:434.576
Hs Code.:

C<sub>24</sub>H<sub>38</sub>N<sub>2</sub>O<sub>5</sub>

Synonyms:C₂₄H₃₈N₂O₅

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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 C₂₄H₃₈N₂O₅

Chemical Property:

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Technology Process of C₂₄H₃₈N₂O₅

There total 5 articles about C₂₄H₃₈N₂O₅ 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: 100.0%

: 4530-20-5
BOC-glycine

: 1336888-76-6
(R)-isopropyl 4-(1-amino-4,4-dimethylpentyl)benzoate hydrochloride

: 1220904-24-4
C₂₄H₃₈N₂O₅

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 0 - 20 ℃; for 16.25h;

Reference yield:

: 619-66-9
4-Carboxybenzaldehyde

: 1220904-24-4
C₂₄H₃₈N₂O₅

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium carbonate / N,N-dimethyl-formamide; tetrahydrofuran / 64 h / 70 °C

2.1: caesium carbonate / dichloromethane / 30 h / 42 °C

3.1: magnesium / iodine / diethyl ether / 2.75 h / Inert atmosphere; Reflux

3.2: 2 h / -78 - 20 °C

3.3: 1 h / 0 - 20 °C

4.1: hydrogenchloride / 1,4-dioxane; methanol / 1.5 h / 20 °C

5.1: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / acetonitrile / 16.25 h / 0 - 20 °C

With hydrogenchloride; potassium carbonate; benzotriazol-1-ol; caesium carbonate; magnesium; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; iodine; In tetrahydrofuran; 1,4-dioxane; methanol; diethyl ether; dichloromethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 70240-29-8
4-(isopropyloxycarbonyl)benzaldehyde

: 1220904-24-4
C₂₄H₃₈N₂O₅

Guidance literature:: Multi-step reaction with 4 steps

1.1: caesium carbonate / dichloromethane / 30 h / 42 °C

2.1: magnesium / iodine / diethyl ether / 2.75 h / Inert atmosphere; Reflux

2.2: 2 h / -78 - 20 °C

2.3: 1 h / 0 - 20 °C

3.1: hydrogenchloride / 1,4-dioxane; methanol / 1.5 h / 20 °C

4.1: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / acetonitrile / 16.25 h / 0 - 20 °C

With hydrogenchloride; benzotriazol-1-ol; caesium carbonate; magnesium; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; iodine; In 1,4-dioxane; methanol; diethyl ether; dichloromethane; acetonitrile;