-L-glutamic acid 1-methylamide 5-benzyl ester

Base Information

Chemical Name:-L-glutamic acid 1-methylamide 5-benzyl ester
CAS No.:216309-87-4
Molecular Formula:C₃₀H₄₁N₃O₁₄
Molecular Weight:667.667
Hs Code.:

<O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-L-seryl>-L-glutamic acid 1-methylamide 5-benzyl ester

Synonyms:-L-glutamic acid 1-methylamide 5-benzyl ester

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Chemical Property of -L-glutamic acid 1-methylamide 5-benzyl ester

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Technology Process of -L-glutamic acid 1-methylamide 5-benzyl ester

There total 5 articles about -L-glutamic acid 1-methylamide 5-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: 70.1%

: 211678-12-5
-L-glutamic acid 1-methylamide 5-benzyl ester

: 216309-87-4
-L-glutamic acid 1-methylamide 5-benzyl ester

Guidance literature:: With morpholine; In N,N-dimethyl-formamide; for 1.5h; Ambient temperature;
DOI:10.1021/jm980267x

Reference yield:

: 83-87-4,604-68-2,604-69-3,2152-77-4,4026-35-1,4163-59-1,4163-60-4,4163-61-5,4163-65-9,4257-94-7,4257-96-9,16299-15-3,19186-39-1,19189-55-0,25878-60-8,25941-03-1,32445-48-0,32445-49-1,32445-53-7,32445-54-8,34685-58-0,34685-59-1,43168-42-9,43168-44-1,43169-22-8,43169-25-1,66966-07-2,70749-17-6,80184-01-6,93221-01-3,93221-02-4,99630-88-3,109215-53-4,115792-70-6,115792-73-9,139894-92-1,139973-25-4,144071-49-8,147648-81-5
D-Mannose pentaacetate

: 216309-87-4
-L-glutamic acid 1-methylamide 5-benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 63.5 percent / BF₃*OEt₂ / CHCl₃ / 21 h / Ambient temperature

2: Et₃N, WSC, HOBt / dimethylformamide / 18 h / Ambient temperature

3: 70.1 percent / morpholine / dimethylformamide / 1.5 h / Ambient temperature

With morpholine; boron trifluoride diethyl etherate; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; In chloroform; N,N-dimethyl-formamide;
DOI:10.1021/jm980267x

Reference yield:

: 56698-52-3
benzyl N-tert-butyloxycarbonyl-L-γ-glutamate α-N-methylamide

: 216309-87-4
-L-glutamic acid 1-methylamide 5-benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: HCl / dioxane / 0.25 h / Ambient temperature

2: Et₃N, WSC, HOBt / dimethylformamide / 18 h / Ambient temperature

3: 70.1 percent / morpholine / dimethylformamide / 1.5 h / Ambient temperature

With morpholine; hydrogenchloride; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; In 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.1021/jm980267x