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Synthetic method of pyroglutamyl small peptide

A pyroglutamine-based, synthetic method technology, applied in the field of pyroglutamine-based small peptide synthesis, to achieve the effects of avoiding yield loss, simple operation, and less by-products

Inactive Publication Date: 2011-04-20
XIAMEN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0010] The purpose of the present invention is to solve the problems that the existing pyroglutamine-based small peptide synthesis method requires the activation of the carboxyl end of pyroglutamic acid while protecting the carboxyl end of another amino acid, and to provide a cheap and easy-to-obtain raw material with high yield and high yield. Synthesis method of pyroglutamine-based small peptides with simple post-processing and more suitable for large-scale production

Method used

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  • Synthetic method of pyroglutamyl small peptide

Examples

Experimental program
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Effect test

Embodiment 1

[0031] Embodiment 1: Add 1.04g (4.68mmol) pyroglutamyl cyclic bis-condensate in the 25mL round bottom flask that reflux condenser is housed, 0.75g (10mmol) glycine, 10mL trifluoroethanol and 1.38mL (10mmol) triethylamine. The mixture was heated and stirred at 70°C overnight. After concentration under reduced pressure, purification by column chromatography (eluent: isopropanol: acetonitrile: ammonia water = 10:10:1) yielded 1.48 g of white L-pyroglutamic acid-glycine dipeptide solid with a yield of 85%. 1 H NMR (D 2 O): δ (ppm) 2.06-2.15 (1H, m), 2.35-2.47 (2H, m), 2.48-2.58 (1H, m), 3.82 (2H, s), 4.35 (1H, dd, J=9.04 Hz, 5.28Hz); 13 CNMR (D 2 O): δ (ppm) 25.0, 29.2, 42.6, 57.1, 174.9, 175.6, 182.4; ESI-MS (m / z): 187 [M+H] + , 209[M+Na] + .

Embodiment 2

[0032] Example 2: L-pyroglutamic acid-β-alanine dipeptide (L-pGlu-β-Ala-OH): add 1.04g (4.68mmol) coke in a 25mL round bottom flask equipped with a reflux condenser Glutaminyl cyclic bis-condensate, 0.89 g (10 mmol) β-alanine, 7 mL trifluoroethanol and 1.74 mL (10 mmol) diisopropylethylamine. The mixture was stirred with heating at 0 °C overnight. After concentration under reduced pressure, purification by column chromatography (eluent: isopropanol: acetonitrile: ammonia water = 10:10:1) yielded 1.11 g of colorless viscous L-pyroglutamic acid-β-alanine dipeptide , yield 59%. 1 H NMR (D 2 O): δ (ppm) 1.98-2.07 (1H, m), 2.32-2.42 (2H, m), 2.44-2.54 (1H, m), 2.46 (2H, t, J=6.72Hz), 3.43 (2H, t, J = 6.32Hz), 4.26 (1H, dd, J = 9.04Hz, 5.20Hz), 4.41 (1H, dd, J = 8.24Hz, 5.00Hz); 13 C NMR (D 2 O): δ (ppm) 25.2, 29.3, 35.2, 36.1, 57.1, 174.8, 178.4, 182.3; ESI-MS (m / z): 201 [M+H] + , 223[M+Na] + .

Embodiment 3

[0033] Example 3: L-pyroglutamic acid-L-aspartic acid dipeptide (L-pGlu-L-Asp-OH): Add 1.04g (4.68mmol) in a 25mL round bottom flask equipped with a reflux condenser Pyroglutaminyl cyclic diacid, 1.33g (10mmol) aspartic acid, 20mL trifluoroethanol and 2.76g (20mmol) potassium carbonate. The mixture was stirred with heating at 40°C overnight. After concentration under reduced pressure, purification by column chromatography (eluent: isopropanol: acetonitrile: ammonia water = 5:5:1) yielded 0.75 g of white L-pyroglutamic acid-L-aspartic acid dipeptide solid, Yield 33%. 1 H NMR (D 2 O): δ (ppm) 2.01-2.09 (1H, m), 2.34-2.40 (2H, m), 2.44-2.55 (1H, m), 2.88 (1H, d, J = 17.00Hz, 7.36Hz), 2.96 (1H, d, J = 17.02Hz, 5.08Hz), 4.32 (1H, dd, J = 9.06Hz, 4.88Hz), 4.74 (1H, dd, J = 6.94Hz, 5.48Hz); 13 C NMR (D 2 O): δ (ppm) 25.1, 29.2, 35.4, 49.2, 56.8, 173.9, 174.4, 174.8, 182.3; ESI-MS (m / z): 245 [M+H] + , 267[M+Na] + .

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Abstract

The invention discloses a synthetic method of pyroglutamyl small peptide, relates to a synthetic method of pyroglutamyl small peptide and provides a synthetic method of pyroglutamyl small peptide which has low-price and easily obtained raw materials, high productivity, simple post treatment and is more suitable for large-scale production. 10mmol of pyroglutamyl diketopiperazine, 20 to 30mmol of amino acid or small peptide and 20 to 30mmol of alkaline organic solvent are added into a container which has a volume of 25mL and is provided with a reflux condensing pipe; the mixture is stirred at the temperature of 0 DEG C to 70 DEG C, reacts for a night, and then undergoes vacuum concentration and then column chromatography and purification to obtain the pyroglutamyl small peptide with the productivity of 20 percent to 85 percent.

Description

technical field [0001] The invention relates to a method for synthesizing pyroglutamine-based small peptides, which comprises the steps of synthesizing di-focused glutamic acid with pyroglutamic acid as a raw material, and then reacting with amino acids or small peptides in an organic solvent in the presence of a base to obtain the corresponding Pyroglutamine-based small peptides. Background technique [0002] The traditional synthesis method of dipeptide is the condensation of dicyclohexylcarbodiimide (DCC). As far back as 1986, S.A.Andronati etc. (Andronati, S.A.; Mazurov, A.A.; Korotenko, T.I., Khimiya Prirodnykh Soedinenii, 1986,2,222-224) just used dicyclohexylcarbodiimide (DCC) as condensation agent in N- Synthesis of pyroglutaminyl histidine dipeptide in the presence of hydroxysuccinimide (HOSu). The yield of this method is higher, and the literature report can reach up to 90%, but the by-product dicyclohexyl urea (DCU) produced by the reaction will bring troubles t...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07K5/078C07K1/16
Inventor 赵玉芬郭剑南金轶唐果许鹏翔
Owner XIAMEN UNIV
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