C₂₅H₃₂N₂O₅

Base Information

Chemical Name:C₂₅H₃₂N₂O₅
CAS No.:1415034-01-3
Molecular Formula:C₂₅H₃₂N₂O₅
Molecular Weight:440.539
Hs Code.:

C<sub>25</sub>H<sub>32</sub>N<sub>2</sub>O<sub>5</sub>

Synonyms:

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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 C₂₅H₃₂N₂O₅

Chemical Property:

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Technology Process of C₂₅H₃₂N₂O₅

There total 1 articles about C₂₅H₃₂N₂O₅ 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:

: 15761-38-3
L-N-Boc-Ala

: H-D-(N-Me)Phe-OCH₂Ph

: 1415034-01-3
C₂₅H₃₂N₂O₅

Guidance literature:: With 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; Cooling with ice;
DOI:10.1021/jm301630s

Reference yield:

: 1415034-01-3
C₂₅H₃₂N₂O₅

: C₂₀H₂₄N₂O₃

Guidance literature:: With hydrogenchloride; water; In ethyl acetate; at 20 ℃; for 1h;
DOI:10.1021/jm301630s

Reference yield:

: 1415034-01-3
C₂₅H₃₂N₂O₅

: C₂₄H₃₇N₃O₆

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogenchloride; water / ethyl acetate / 1 h / 20 °C

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 1-hydroxy-7-aza-benzotriazole; N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Cooling with ice

3: hydrogen; palladium on activated charcoal / ethyl acetate / 2 h / 760.05 Torr

With hydrogenchloride; 1-hydroxy-7-aza-benzotriazole; palladium on activated charcoal; water; hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; ethyl acetate;
DOI:10.1021/jm301630s