Method of producing peptide
View Patent ↗The present invention is related to a method of producing a peptide, characterized in contacting a reaction mixture with a base after a condensation reaction to hydrolyze while a basic condition is maintained until a ratio of a remaining unreacted active ester of an acid component is decreased to 1% or less in a liquid phase peptide synthesis method. According to the invention, a target peptide of high purity can be simply and efficiently produced by a continuous liquid phase synthesis method. Further, the present invention is related to a method of producing a peptide, characterized in using an amide-type solvent immiscible with water in a liquid phase peptide synthesis method. According to the invention, various peptides can be produced by the liquid phase synthesis method without being restricted by the amino acid sequence of the target peptide.
1. A method of producing a peptide by a liquid phase synthesis method, comprising steps of:
Step A: reacting the active ester of the acid of a first amino acid or a first peptide with the amine of a second amino acid or a second peptide to obtain a first reaction mixture comprising an intermediate peptide, wherein the amine of the first amino acid or the first peptide has a protecting group such that the intermediate peptide has an N-terminal amine protecting group;
Step B: purifying the intermediate peptide contained in the first reaction mixture obtained in Step A, wherein the purification is performed by using an amide-type solvent immiscible with water or a mixed solvent containing the amide-type solvent immiscible with water and a halogenated hydrocarbon-type solvent, and by separating the solvent layer containing the intermediate peptide from an aqueous layer;
Step C: removing the N-terminal amine protecting group of the intermediate peptide obtained in Step B to form a second reaction mixture; and
Step D: purifying the intermediate peptide contained in the second reaction mixture, if necessary.
2. The method according to claim 1 , wherein the amide-type solvent immiscible with water is selected from the group consisting of N,N-dibutylformamide, N,N-dipropylformamide, N,N-dibutylacetamide and N,N-dipropylacetamide.
3. The method according to claim 1 , wherein the amide-type solvent immiscible with water is used in Steps A, B and C.
4. The method according to claim 1 , wherein the acid of the second amino acid or the second peptide in Step A has a protecting group such that the intermediate peptide formed in Step B has a C-terminal acid protecting group.
5. The method according to claim 1 , wherein Step D is conducted under an acidic condition for crystallization.
6. The method according to claim 1 , wherein the intermediate peptide in Step D is purified by crystallization.
7. The method according to claim 1 , wherein a mixed solvent containing the amide-type solvent immiscible with water and a halogenated hydrocarbon-type solvent is used.