C₄₂H₄₅N₅O₆

Base Information

Chemical Name:C₄₂H₄₅N₅O₆
CAS No.:1329063-32-2
Molecular Formula:C₄₂H₄₅N₅O₆
Molecular Weight:715.849
Hs Code.:

C<sub>42</sub>H<sub>45</sub>N<sub>5</sub>O<sub>6</sub>

Synonyms:C₄₂H₄₅N₅O₆

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Chemical Property of C₄₂H₄₅N₅O₆

Chemical Property:

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Technology Process of C₄₂H₄₅N₅O₆

There total 18 articles about C₄₂H₄₅N₅O₆ 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: 80.0%

: 1329063-41-3
C₃₄H₃₉N₅O₅*ClH

: 103-80-0
phenylacetyl chloride

: 1329063-32-2
C₄₂H₄₅N₅O₆

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 6h; Inert atmosphere;
DOI:10.1021/jm200608k

Reference yield:

: 1329063-38-8
(2S)-(3-pyridyl)alaninyl-(3S)-β-homophenylalaninyl benzyl ester hydrochloride

: C₂₄H₂₄N₂O₄

: 1329063-32-2
C₄₂H₄₅N₅O₆

: C₄₂H₄₃N₅O₆

Guidance literature:: C₂₄H₂₄N₂O₄; With palladium 10% on activated carbon; hydrogen; In methanol; under 760.051 Torr;

With benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; In dichloromethane; for 0.25h;

(2S)-(3-pyridyl)alaninyl-(3S)-β-homophenylalaninyl benzyl ester hydrochloride; With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 6h;
DOI:10.1021/acs.jmedchem.9b00056

Reference yield:

: 100-39-0
benzyl bromide

: 1329063-32-2
C₄₂H₄₅N₅O₆

Guidance literature:: Multi-step reaction with 7 steps

1.1: caesium carbonate / water; acetonitrile / 1 h / Inert atmosphere

1.2: Inert atmosphere

2.1: trifluoroacetic acid / dichloromethane / 20 °C / Inert atmosphere

2.2: 1 h / Inert atmosphere

3.1: benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / dichloromethane / 0.25 h / 20 °C / Inert atmosphere

3.2: 3 h / Inert atmosphere

4.1: trifluoroacetic acid / dichloromethane / 20 °C / Inert atmosphere

4.2: 1 h / Inert atmosphere

5.1: benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / dichloromethane / 0.25 h / 20 °C / Inert atmosphere

5.2: 6 h / 20 °C / Inert atmosphere

6.1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C / Inert atmosphere

6.2: Inert atmosphere

7.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 6 h / 20 °C / Inert atmosphere

With benzotriazol-1-ol; caesium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In dichloromethane; water; acetonitrile;
DOI:10.1021/jm200608k