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.:123418-24-6
Molecular Formula:C₄₃H₅₉N₅O₁₇
Molecular Weight:917.965
Hs Code.:

N-(2-O-<benzyl 2-acetamido-6-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-4-O-acetyl-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 5 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: 12.0%

: 110582-59-7
N-(2-O--(R)-lactoyl)-L-alanyl-D-isoglutamine benzyl ester

: 123418-26-8
N-(2-O--(R)-lactoyl)-L-alanyl-D-glutamine methyl ester

: 123418-25-7
N-(2-O--(R)-lactoyl)-L-alanyl-D-isoglutamine methyl ester

: 123418-24-6
N-(2-O--(R)-lactoyl)-L-alanyl-D-isoglutamine benzyl ester

Guidance literature:: With magnesium oxide; In methanol; chloroform; for 48h; 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)

: 123418-24-6
N-(2-O--(R)-lactoyl)-L-alanyl-D-isoglutamine benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) N-methylmorpholine, isobutyl chloroformate / 1.) tetrahydrofuran, 15 min, 2.) N,N-dimethylformamide, -15 deg C, 1 h, room temperature, 5 h

2: 12 percent / MgO / methanol; CHCl₃ / 48 h / Ambient temperature

With 4-methyl-morpholine; magnesium oxide; isobutyl chloroformate; In methanol; chloroform;
DOI:10.1016/0008-6215(89)84005-4

Reference yield:

: 107671-47-6
benzyl 2-acetamido-6-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)-4-O-acetyl-2-deoxy-3-O-<(R)-1-carboxyethyl>-α-D-glucopyranoside

: 123418-24-6
N-(2-O--(R)-lactoyl)-L-alanyl-D-isoglutamine benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) N-methylmorpholine, isobutyl chloroformate / 1.) tetrahydrofuran, 15 min, 2.) N,N-dimethylformamide, -15 deg C, 1 h, room temperature, 5 h

2: 12 percent / MgO / methanol; CHCl₃ / 48 h / Ambient temperature

With 4-methyl-morpholine; magnesium oxide; isobutyl chloroformate; In methanol; chloroform;
DOI:10.1016/0008-6215(89)84005-4