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869001-94-5

  • Product Name:L-Glutamic acid, N-[(phenylmethoxy)carbonyl]glycyl-2-methyl-L-prolyl-,bis(phenylmethyl) ester
  • Molecular Formula:C35H39N3O8
  • Molecular Weight:629.71
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Product Details

Purity:99%

Reputable factory supply L-Glutamic acid, N-[(phenylmethoxy)carbonyl]glycyl-2-methyl-L-prolyl-,bis(phenylmethyl) ester 869001-94-5 in bulk at low price

  • Molecular Formula:C35H39N3O8
  • Molecular Weight:629.71

869001-94-5 Relevant articles

TREATMENT OF AUTISM SPECTRUM DISORDERS USING GLYCYL-L-2-METHYLPROLYL-L-GLUTAMIC ACID

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Page/Page column 32; 34; 35, (2014/06/23)

This invention provides compounds, compo...

TREATMENT OF AUTISM SPECTRUM DISORDERES USING GLYCYL-L-2-METHYLPROLYL-L-GLUTAMIC ACID

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Page/Page column 29; 31; 32, (2012/08/08)

This invention provides compounds, compo...

Synthesis of proline-modified analogues of the neuroprotective agent glycyl-L-prolyl-glutamic acid (GPE)

Harris, Paul W.R.,Brimble, Margaret A.,Muir, Victoria J.,Lai, Michelle Y.H.,Trotter, Nicholas S.,Callis, David J.

, p. 10018 - 10035 (2007/10/03)

The synthesis of ten proline-modified an...

Analogues of the neuroprotective tripeptide Gly-Pro-Glu (GPE): Synthesis and structure-activity relationships

Alonso De Diego, Sergio A.,Munoz, Pilar,Gonzalez-Muniz, Rosario,Herranz, Rosario,Martin-Martinez, Mercedes,Cenarruzabeitia, Edurne,Frechilla, Diana,Del Rio, Joaquin,Jimeno, M. Luisa,Garcia-Lopez, M. Teresa

, p. 2279 - 2283 (2007/10/03)

A series of GPE analogues, including mod...

869001-94-5 Process route

N-benzyloxycarbonyl-glycyl-L-2-methylproline
869001-86-5

N-benzyloxycarbonyl-glycyl-L-2-methylproline

L-glutamic acid dibenzyl ester 4-toluenesulfonate
2791-84-6,227205-81-4

L-glutamic acid dibenzyl ester 4-toluenesulfonate

dibenzyl N-benzyloxycarbonyl-glycyl-L-2-methylprolyl-L-glutamate
869001-94-5

dibenzyl N-benzyloxycarbonyl-glycyl-L-2-methylprolyl-L-glutamate

Conditions
Conditions Yield
With bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; triethylamine; In dichloromethane; at 20 ℃; for 17h;
89%
N-benzyloxycarbonyl-glycyl-L-2-methylproline; L-glutamic acid dibenzyl ester 4-toluenesulfonate; With triethylamine; In dichloromethane; at 20 ℃; for 0.166667h; Inert atmosphere;
With bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; In dichloromethane; for 17h;
89%
N-benzyloxycarbonyl-glycyl-L-2-methylproline; L-glutamic acid dibenzyl ester 4-toluenesulfonate; With triethylamine; In dichloromethane; at 20 ℃; for 0.166667h; Inert atmosphere;
With bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; In dichloromethane; at 20 ℃; for 17h; Inert atmosphere;
89%
methyl (S)-2-methylpyrrolidine-2-carboxylate monohydrochloride
220060-08-2,51098-46-5,1286768-32-8

methyl (S)-2-methylpyrrolidine-2-carboxylate monohydrochloride

dibenzyl N-benzyloxycarbonyl-glycyl-L-2-methylprolyl-L-glutamate
869001-94-5

dibenzyl N-benzyloxycarbonyl-glycyl-L-2-methylprolyl-L-glutamate

Conditions
Conditions Yield
Multi-step reaction with 3 steps
1: 92 percent / triethylamine; bis(2-oxo-3-oxazolidinyl)phosphinic chloride / CH2Cl2 / 20.5 h / 20 °C
2: 90 percent / aqueous sodium hydroxide / dioxane / 19 h / 20 °C
3: 89 percent / triethylamine; bis(2-oxo-3-oxazolidinyl)phosphinic chloride / CH2Cl2 / 17 h / 20 °C
With sodium hydroxide; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; triethylamine; In 1,4-dioxane; dichloromethane;
Multi-step reaction with 3 steps
1.1: triethylamine / dichloromethane / 0.33 h / 0 °C / Inert atmosphere
1.2: 0 - 20 °C
2.1: sodium hydroxide; water / 1,4-dioxane / 19 h / 20 °C
3.1: triethylamine / dichloromethane / 0.17 h / 20 °C / Inert atmosphere
3.2: 17 h
With water; triethylamine; sodium hydroxide; In 1,4-dioxane; dichloromethane;
Multi-step reaction with 3 steps
1.1: triethylamine / dichloromethane / 0.33 h / 0 °C / Inert atmosphere
1.2: 20 h / 0 - 20 °C
2.1: sodium hydroxide; water / 1,4-dioxane / 19 h / 20 °C
3.1: triethylamine / dichloromethane / 0.17 h / 20 °C / Inert atmosphere
3.2: 17 h / 20 °C / Inert atmosphere
With water; triethylamine; sodium hydroxide; In 1,4-dioxane; dichloromethane;

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869001-94-5 Downstream products

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