N-(2-O--(R)-lactoyl)-L-alanyl-D-isoglutamine benzyl ester

Base Information

Chemical Name:N-(2-O--(R)-lactoyl)-L-alanyl-D-isoglutamine benzyl ester
CAS No.:123418-21-3
Molecular Formula:C₄₇H₆₃N₅O₁₉
Molecular Weight:1002.04
Hs Code.:

N-(2-O-<benzyl 2-acetamido-6-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)-2,3-dideoxy-α-D-glucopyranosid-3-yl>-(R)-lactoyl)-L-alanyl-D-isoglutamine benzyl ester

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Chemical Property of N-(2-O--(R)-lactoyl)-L-alanyl-D-isoglutamine benzyl ester

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Technology Process of N-(2-O--(R)-lactoyl)-L-alanyl-D-isoglutamine benzyl ester

There total 2 articles about N-(2-O--(R)-lactoyl)-L-alanyl-D-isoglutamine benzyl 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: 44.0%

: 62853-36-5,71822-09-8,85546-24-3
L-alanyl-(γ-benzyl ester D-isoglutamine)

: 95900-07-5
benzyl 2-acetamido-6-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)-3-O-<(R)-1-carboxyethyl>-2-deoxy-α-D-glucopyranoside 1',4-lactone

: 123418-21-3
N-(2-O--(R)-lactoyl)-L-alanyl-D-isoglutamine benzyl ester

Guidance literature:: With 1H-imidazole; tetra-n-hexylammonium benzoate; In 1,4-dioxane; for 288h; Ambient temperature;
DOI:10.1016/0008-6215(89)84005-4

Reference yield:

: 62853-36-5,71822-09-8,85546-24-3
L-alanyl-(γ-benzyl ester D-isoglutamine)

: 107671-46-5
benzyl 2-acetamido-6-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)-2-deoxy-3-O-<(R)-1-carboxyethyl>-α-D-glucopyranoside

: 123418-21-3
N-(2-O--(R)-lactoyl)-L-alanyl-D-isoglutamine benzyl ester

: 95900-08-6
benzyl 2-acetamido-6-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)-2-deoxy-3-O-<(R)-1-(methoxycarbonyl)ethyl>-α-D-glucopyranoside

: 95900-07-5
benzyl 2-acetamido-6-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)-3-O-<(R)-1-carboxyethyl>-2-deoxy-α-D-glucopyranoside 1',4-lactone

Guidance literature:: With 4-methyl-morpholine; isobutyl chloroformate; Yield given. Multistep reaction; 1.) tetrahydrofuran, 15 min, 2.) N,N-dimethylformamide, -15 deg C, 1 h, room temperature, 5 h;
DOI:10.1016/0008-6215(89)84005-4

Reference yield:

: 123418-21-3
N-(2-O--(R)-lactoyl)-L-alanyl-D-isoglutamine benzyl ester

: 123418-23-5
N-(2-O--(R)-lactoyl)-L-alanyl-D-glutamine methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine

2: 17 percent / 0.1M NaOMe / 3 h / Ambient temperature

With sodium methylate; In pyridine;
DOI:10.1016/0008-6215(89)84005-4