N-<1-glycyl>-trans-3-<4-(1-hydroxy-2-nitroethyl)phenoxy>-L-prolyl-L-isoleucine methyl ester

Base Information

Chemical Name:N-<1-glycyl>-trans-3-<4-(1-hydroxy-2-nitroethyl)phenoxy>-L-prolyl-L-isoleucine methyl ester
CAS No.:129575-00-4
Molecular Formula:C₂₇H₄₀N₄O₁₀
Molecular Weight:580.635
Hs Code.:

N-<1-<N-(1,1-dimethylethoxy)carbonyl>glycyl>-trans-3-<4-(1-hydroxy-2-nitroethyl)phenoxy>-L-prolyl-L-isoleucine methyl ester

Synonyms:N-<1-glycyl>-trans-3-<4-(1-hydroxy-2-nitroethyl)phenoxy>-L-prolyl-L-isoleucine methyl ester

Suppliers and Price of N-<1-glycyl>-trans-3-<4-(1-hydroxy-2-nitroethyl)phenoxy>-L-prolyl-L-isoleucine methyl ester

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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 N-<1-glycyl>-trans-3-<4-(1-hydroxy-2-nitroethyl)phenoxy>-L-prolyl-L-isoleucine methyl ester

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Technology Process of N-<1-glycyl>-trans-3-<4-(1-hydroxy-2-nitroethyl)phenoxy>-L-prolyl-L-isoleucine methyl ester

There total 2 articles about N-<1-glycyl>-trans-3-<4-(1-hydroxy-2-nitroethyl)phenoxy>-L-prolyl-L-isoleucine methyl ester 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: 93.6%

: 75-52-5
nitromethane

: 129574-99-8
N-<1-glycyl>-trans-3-<4-(formylphenoxy)-L-prolyl>-L-isoleucine methyl ester

: 129575-00-4
N-<1-glycyl>-trans-3-<4-(1-hydroxy-2-nitroethyl)phenoxy>-L-prolyl-L-isoleucine methyl ester

Guidance literature:: With sodium methylate; at 0 ℃; for 3.5h;

Reference yield:

: 123043-38-9,123043-39-0
N-trans-3-(4-cyanophenoxy)-1-glycyl>-L-prolyl-L-isoleucine methyl ester

: 129575-00-4
N-<1-glycyl>-trans-3-<4-(1-hydroxy-2-nitroethyl)phenoxy>-L-prolyl-L-isoleucine methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 76.4 percent / Raney Ni, NaH₂PO₂*H₂O, buffer 2:1:1 pyridine: acetic acid: water / 4 h / 55 - 60 °C

2: 93.6 percent / sodium methoxide / 3.5 h / 0 °C

With sodium hypophosphite; buffer 2:1:1 pyridine: acetic acid: water; sodium methylate; nickel; isobutyric Acid;