Solid phase process for synthesizing peptides

Claim 2

In a solid phase peptide synthesis process for producing a peptide amide having the amino acid sequence represented by the formula Y p -X-NH 2 where Yp represents the N-terminal peptide fragment, and X-NH. 2 represents the C-terminal amino acid having an amide group (-CONH 2 )in its molecular structure by forming the peptide having the above sequence bonded to a resin, said peptide optionally having one or more protected functional groups and cleaving the peptide from the resin and deprotecting protected functional groups; the improvement comprising forming the peptide bonded to methylbenzhydrylamine resin and cleaving and deprotecting the resin bound peptide with hydrogen bromide.

Claim 3

The process of claim I wherein the peptide bonded to methylbenzhydrylamine resin is suspended in trifluoroacetic acid and anhydrous hydrogen bromide gas is blown into the suspension to effect cleavage and deprotection.

Claim 4

The process of claim 1 wherein a mixture of hydrogen bromide gas and anisole is used to effect cleavage and deprotection.

Claim 5

The method of claim 1 wherein a mixture of hydrogen bromide, anisole and thioanisole is used to effect cleavage and deprotection.

Claim 6

The method of claim 4 wherein the volume ratio of anisole to thioanisole is from about 20:80 to about 80:20.

Claim 7

The method of claim 4 wherein the volume ratio of anisole to thioanisole is about 1:1.

Claim 8

In a solid phase peptide synthesis process for producing a peptide of a desired amino acid sequence by the steps of (a) temporarily chemically protecting the reactive amino group and any other reactive groups, other than the carboxylic acid group at the alpha-position, on the C-terminal amino acid of the peptide; (b) chemically binding the protected C-terminal amino acid via the carboxylic acid (-COOH) group thereof to a resin support; (c) chemically deprotecting the reactive amino group of the resin-bound protected amino acid; (d) chemically coupling via a peptide bond the next amino acid in the desired sequence by contacting the resin-bound amino acid from step (c) with the next amino acid in the desired sequence with all of the reactive groups thereof, other than the carboxylic acid group at the alpha-position, chemically protected, in the presence of a coupling agent; (e) chemically deprotecting the reactive amino group of the coupled amino acid from step (d); (f) continuing the synthesis by repeating steps (d) and (e) with successive amino acids in the desired sequence being added one at a time until the total desired sequence of the protected peptide is built up on the resin; and (g) cleaving the protected peptide from the resin support and deprotecting protected reaction groups; the improvement comprising in step (g) contacting the resin bound protected peptide with a mixture of hydrogen bromide, anisole and thioanisole to simultaneously cleave the protected peptide from the resin support and remove the protecting groups.

Claim 9

In a solid phase peptide synthesis process for producing a peptide of a desired amino acid sequence by the steps of (a) temporarily chemically protecting the reactive amino group and any other reactive groups, other than the carboxylic acid group at the alpha-position, on the C-terminal amino acid of the peptide; (b) chemically binding the protected C-terminal amino acid via the carboxylic acid (-COOH) group thereof to a resin support; (c) chemically deprotecting the reactive amino group of the resin-bound protected amino acid; (d) chemically coupling via a peptide bond the next amino acid in the desired sequence by contacting the resin-bound amino acid from step (c) with the next amino acid in the desired sequence with all of the reactive groups thereof, other than the carboxylic acid group at the alpha-position, chemically protected, in the presence of a coupling agent; (e) chemically deprotecting the reactive amino group of the coupled amino acid from step (d); (f) continuing the synthesis by repeating steps (d) and (e) with successive amino acids in the desired sequence being added one at a time until the total desired sequence of the protected peptide is built up on the resin; and (g) cleaving the protected peptide from the resin support and deprotecting protected reaction groups; the improvement comprising in step (g) contacting the resin bound protected peptide with a mixture of hydrogen bromide, anisole and thioanisole to simultaneously cleave the protected peptide from the resin support and remove the protecting groups.

Claim 10

The process of claim 7 wherein the anisole and thioanisole are present at a volume ratio of from about 1:4 to about 4:1.

Claim 11

'9. The process of claim 7 wherein the anisole and thioanisole are present at a volume ratio of about 1:1.

Claim 12

The process of claim 7 wherein prior to step (g).the resin bound protected peptide is suspended in trifluoroacetic acid.

Claim 13

The process of claim 7 wherein the resin support is selected from the group consisting of chloromethylated polystyrene resin and methylbenzhydrylamine resin.

Claim 14

In a solid phase synthesis of the thymosin α 1 , polypeptide having the sequence: Asn-OH by forming the polypeptide having the above sequence anchored to a resin, said polypeptide optionally having one or more protected functional groups; and clenving the polypeptide from the resin and deprotecting protocted fencetinal groups of the polypeptide; the improvement aomprising using methylbenzhydrylamine resin and cleaving and deprotecting the polypeptide by contacting the polypeptide with hydrogen bromide.

Claim 15

In a solid phase synthesis of the thymosin α 1 , polypeptide having the sequence: Asn-OH by forming the polypeptide having the above sequence anchored to a resin, said polypeptide optionally having one or more protected functional groups; and clenving the polypeptide from the resin and deprotecting protocted fencetinal groups of the polypeptide; the improvement aomprising using methylbenzhydrylamine resin and cleaving and deprotecting the polypeptide by contacting the polypeptide with hydrogen bromide.

Claim 16

The process of claim 12 wherein the methylbenzhydrylamine resin bound'polypeptide is cleaved and deprotected with a mixture of anhydrous hydrogen bromide gas in trifluoroacetic acid.

Claim 17

The process of claim 13 wherein the mixture additionally comprises anisole.

Claim 18

The process of claim 14 wherein the mixture additionally comprises thioanisole.

Claim 19

The process of claim 15 wherein the volume ratio of anisole to thioanisole is from about 1:4 to about 4:1..

Claim 20

The process of claim 15 wherein the volume ratio of anisole to thioanisole is about 1:1.

Claim 21

In a solid phase synthesis of the N-terminal 14 amino acid partial sequence of thymosin a l having the following sequence: by forming a protected polypeptide having the above sequence anchored to a benzyl ester resin; and cleaving the polypeptide from the resin and deprotecting the polypeptide; the improvement comprising cleaving and deprotecting the polypeptide by contacting the polypeptide with a mixture of anhydrous hydrogen bromide, anisole and thioanisole.

Claim 22

In a solid phase synthesis of the N-terminal 14 amino acid partial sequence of thymosin a l having the following sequence: by forming a protected polypeptide having the above sequence anchored to a benzyl ester resin; and cleaving the polypeptide from the resin and deprotecting the polypeptide; the improvement comprising cleaving and deprotecting the polypeptide by contacting the polypeptide with a mixture of anhydrous hydrogen bromide, anisole and thioanisole.

Claim 23

The process of claim 18 wherein the volume ratio of anisole to thioani-sole is from about 1:4 to about 4:1.

Claim 24

The process of claim 18 wherein the volume ratio of anisole to thioanisole is about 1:1.

Claim 25

The process of claim 18 wherein the cleavage and deprotection are carried out in trifluoroacetic acid.