Improvements in or relating to the manufacture of peptides, polypeptides and derivatives thereof

A mixed anhydride of an N-substituted aminocarboxylic acid and sulphuric acid is made by reacting a salt of the N-substituted amino-carboxylic acid with sulphur trioxide under anhydrous conditions. The anhydride contains the group -CO.O.SO3H. On reacting the anhydride with the salt of a peptide, pol...

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description A mixed anhydride of an N-substituted aminocarboxylic acid and sulphuric acid is made by reacting a salt of the N-substituted amino-carboxylic acid with sulphur trioxide under anhydrous conditions. The anhydride contains the group -CO.O.SO3H. On reacting the anhydride with the salt of a peptide, polypeptide or an aminocarboxylic acid having an unsubstituted amino group peptides, polypeptides or derivatives thereof are obtained. Sulphur trioxide may be used in the form of a complex with dimethylformamide, a tertiary amine, e.g. pyridine, or ether, e.g. dioxane. Complicated or simple polypeptides may be obtained by utilizing as the N-substituted amino-acid, a peptide or polypeptide whose terminal amino-group is protected by a hydrolysable substituent or by using as the salt of the amino-carboxylic acid, a salt of a peptide or polypeptide. Preferably the salt of the amino-carboxylic acid is the salt of an alpha-amino carboxylic acid, e.g. an alkali metal or quaternary ammonium salt. The second reaction is preferably effected under non-acidic conditions with a molar excess of salt. In an illustration of the process a solution of an amino-acid, e.g. a peptide or polypeptide, the amino group of which is protected by a carbobenzyloxy or p-toluenesulphonyl group, in dimethylformamide is neutralized with a methanol solution of potassium methoxide or trimethylphenyl ammonium methoxide and on distillation of a portion of the solvent at 50-55 DEG C. an anhydrous solution of the salt of the amino-acid is obtained. The anhydride is then prepared by the addition of one molecular proportion of sulphur trioxide in dimethylformamide. The addition of an aqueous alkaline solution of an amino-acid, peptide or polypeptide now leads to coupling and the production of the required amino-acid or peptide derivative. The product may be isolated by means of counter current distribution between ethyl acetate and an aqueous solution of a phosphate buffer. The product may be converted into a mixed anhydride and reacted with salts by the process of the invention to produce complex polypeptides. In examples (1) the mixed anhydride of p-toluenesulphonyl - dl - alanine and sulphuric acid is obtained as its potassium salt by neutralizing the amino-acid dissolved in dimethyl-formamide with a methanol solution of potassium methoxide and reacting with sulphur trioxide in dimethylformamide; (2) the anhydride of carbobenzyloxyglycine is made as in (1) and reacted with dl-phenylalanine in aqueous s
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The anhydride contains the group -CO.O.SO3H. On reacting the anhydride with the salt of a peptide, polypeptide or an aminocarboxylic acid having an unsubstituted amino group peptides, polypeptides or derivatives thereof are obtained. Sulphur trioxide may be used in the form of a complex with dimethylformamide, a tertiary amine, e.g. pyridine, or ether, e.g. dioxane. Complicated or simple polypeptides may be obtained by utilizing as the N-substituted amino-acid, a peptide or polypeptide whose terminal amino-group is protected by a hydrolysable substituent or by using as the salt of the amino-carboxylic acid, a salt of a peptide or polypeptide. Preferably the salt of the amino-carboxylic acid is the salt of an alpha-amino carboxylic acid, e.g. an alkali metal or quaternary ammonium salt. The second reaction is preferably effected under non-acidic conditions with a molar excess of salt. In an illustration of the process a solution of an amino-acid, e.g. a peptide or polypeptide, the amino group of which is protected by a carbobenzyloxy or p-toluenesulphonyl group, in dimethylformamide is neutralized with a methanol solution of potassium methoxide or trimethylphenyl ammonium methoxide and on distillation of a portion of the solvent at 50-55 DEG C. an anhydrous solution of the salt of the amino-acid is obtained. The anhydride is then prepared by the addition of one molecular proportion of sulphur trioxide in dimethylformamide. The addition of an aqueous alkaline solution of an amino-acid, peptide or polypeptide now leads to coupling and the production of the required amino-acid or peptide derivative. The product may be isolated by means of counter current distribution between ethyl acetate and an aqueous solution of a phosphate buffer. The product may be converted into a mixed anhydride and reacted with salts by the process of the invention to produce complex polypeptides. In examples (1) the mixed anhydride of p-toluenesulphonyl - dl - alanine and sulphuric acid is obtained as its potassium salt by neutralizing the amino-acid dissolved in dimethyl-formamide with a methanol solution of potassium methoxide and reacting with sulphur trioxide in dimethylformamide; (2) the anhydride of carbobenzyloxyglycine is made as in (1) and reacted with dl-phenylalanine in aqueous sodium hydroxide to yield carbobenzyloxy-glycyl-dl-phenyl alanine; and in (3) and (4) methanol containing phenyltrimethylammonium methoxide is added respectively to carbobenzyloxyglycyl-dl- or l-phenylalanine in dimethylformamide, some solvent removed, sulphur trioxide in dimethylformamide added and then glycine in aqueous sodium hydroxide to yield the corresponding carbobenzyloxyglycyl - phenylalanylglycine. It is stated that the following compounds have been made: p-toluenesulphonyl-dl - alanylglycine, carbobenzyloxy - dl - alanylglycine, carbobenzyloxyglycyl-dl-phenylalanine, carbobenzyloxyglycyl - l - phenylalanine, carbobenzyloxy - l - phenylalanylglycine and p-toluenesulphonyl - glycyl - dl - phenylalanine.</description><language>eng</language><creationdate>1954</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19540901&amp;DB=EPODOC&amp;CC=GB&amp;NR=714834A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25562,76317</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19540901&amp;DB=EPODOC&amp;CC=GB&amp;NR=714834A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>KENNER GEORGE WALLACE</creatorcontrib><title>Improvements in or relating to the manufacture of peptides, polypeptides and derivatives thereof</title><description>A mixed anhydride of an N-substituted aminocarboxylic acid and sulphuric acid is made by reacting a salt of the N-substituted amino-carboxylic acid with sulphur trioxide under anhydrous conditions. The anhydride contains the group -CO.O.SO3H. On reacting the anhydride with the salt of a peptide, polypeptide or an aminocarboxylic acid having an unsubstituted amino group peptides, polypeptides or derivatives thereof are obtained. Sulphur trioxide may be used in the form of a complex with dimethylformamide, a tertiary amine, e.g. pyridine, or ether, e.g. dioxane. Complicated or simple polypeptides may be obtained by utilizing as the N-substituted amino-acid, a peptide or polypeptide whose terminal amino-group is protected by a hydrolysable substituent or by using as the salt of the amino-carboxylic acid, a salt of a peptide or polypeptide. Preferably the salt of the amino-carboxylic acid is the salt of an alpha-amino carboxylic acid, e.g. an alkali metal or quaternary ammonium salt. The second reaction is preferably effected under non-acidic conditions with a molar excess of salt. In an illustration of the process a solution of an amino-acid, e.g. a peptide or polypeptide, the amino group of which is protected by a carbobenzyloxy or p-toluenesulphonyl group, in dimethylformamide is neutralized with a methanol solution of potassium methoxide or trimethylphenyl ammonium methoxide and on distillation of a portion of the solvent at 50-55 DEG C. an anhydrous solution of the salt of the amino-acid is obtained. The anhydride is then prepared by the addition of one molecular proportion of sulphur trioxide in dimethylformamide. The addition of an aqueous alkaline solution of an amino-acid, peptide or polypeptide now leads to coupling and the production of the required amino-acid or peptide derivative. The product may be isolated by means of counter current distribution between ethyl acetate and an aqueous solution of a phosphate buffer. The product may be converted into a mixed anhydride and reacted with salts by the process of the invention to produce complex polypeptides. In examples (1) the mixed anhydride of p-toluenesulphonyl - dl - alanine and sulphuric acid is obtained as its potassium salt by neutralizing the amino-acid dissolved in dimethyl-formamide with a methanol solution of potassium methoxide and reacting with sulphur trioxide in dimethylformamide; (2) the anhydride of carbobenzyloxyglycine is made as in (1) and reacted with dl-phenylalanine in aqueous sodium hydroxide to yield carbobenzyloxy-glycyl-dl-phenyl alanine; and in (3) and (4) methanol containing phenyltrimethylammonium methoxide is added respectively to carbobenzyloxyglycyl-dl- or l-phenylalanine in dimethylformamide, some solvent removed, sulphur trioxide in dimethylformamide added and then glycine in aqueous sodium hydroxide to yield the corresponding carbobenzyloxyglycyl - phenylalanylglycine. It is stated that the following compounds have been made: p-toluenesulphonyl-dl - alanylglycine, carbobenzyloxy - dl - alanylglycine, carbobenzyloxyglycyl-dl-phenylalanine, carbobenzyloxyglycyl - l - phenylalanine, carbobenzyloxy - l - phenylalanylglycine and p-toluenesulphonyl - glycyl - dl - phenylalanine.</description><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1954</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqFi70KAjEQBq-xEPUVZB9AC7kDbVX86-3PcPmigSQbkr2Ab28Kra2GgZlp87j5mLjAI0gmG4gTJTglNjxJmOQF8iqMRg0yJhAbiohiNfKKIrv3z0gFTRrJlvqW6vVMYDNvJka5jMWXs2Z5Pt2P1zUi98hRDQiQ_nLYbrpd2-3bv8EHo6s8pA</recordid><startdate>19540901</startdate><enddate>19540901</enddate><creator>KENNER GEORGE WALLACE</creator><scope>EVB</scope></search><sort><creationdate>19540901</creationdate><title>Improvements in or relating to the manufacture of peptides, polypeptides and derivatives thereof</title><author>KENNER GEORGE WALLACE</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_GB714834A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1954</creationdate><toplevel>online_resources</toplevel><creatorcontrib>KENNER GEORGE WALLACE</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>KENNER GEORGE WALLACE</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Improvements in or relating to the manufacture of peptides, polypeptides and derivatives thereof</title><date>1954-09-01</date><risdate>1954</risdate><abstract>A mixed anhydride of an N-substituted aminocarboxylic acid and sulphuric acid is made by reacting a salt of the N-substituted amino-carboxylic acid with sulphur trioxide under anhydrous conditions. The anhydride contains the group -CO.O.SO3H. On reacting the anhydride with the salt of a peptide, polypeptide or an aminocarboxylic acid having an unsubstituted amino group peptides, polypeptides or derivatives thereof are obtained. Sulphur trioxide may be used in the form of a complex with dimethylformamide, a tertiary amine, e.g. pyridine, or ether, e.g. dioxane. Complicated or simple polypeptides may be obtained by utilizing as the N-substituted amino-acid, a peptide or polypeptide whose terminal amino-group is protected by a hydrolysable substituent or by using as the salt of the amino-carboxylic acid, a salt of a peptide or polypeptide. Preferably the salt of the amino-carboxylic acid is the salt of an alpha-amino carboxylic acid, e.g. an alkali metal or quaternary ammonium salt. The second reaction is preferably effected under non-acidic conditions with a molar excess of salt. In an illustration of the process a solution of an amino-acid, e.g. a peptide or polypeptide, the amino group of which is protected by a carbobenzyloxy or p-toluenesulphonyl group, in dimethylformamide is neutralized with a methanol solution of potassium methoxide or trimethylphenyl ammonium methoxide and on distillation of a portion of the solvent at 50-55 DEG C. an anhydrous solution of the salt of the amino-acid is obtained. The anhydride is then prepared by the addition of one molecular proportion of sulphur trioxide in dimethylformamide. The addition of an aqueous alkaline solution of an amino-acid, peptide or polypeptide now leads to coupling and the production of the required amino-acid or peptide derivative. The product may be isolated by means of counter current distribution between ethyl acetate and an aqueous solution of a phosphate buffer. The product may be converted into a mixed anhydride and reacted with salts by the process of the invention to produce complex polypeptides. In examples (1) the mixed anhydride of p-toluenesulphonyl - dl - alanine and sulphuric acid is obtained as its potassium salt by neutralizing the amino-acid dissolved in dimethyl-formamide with a methanol solution of potassium methoxide and reacting with sulphur trioxide in dimethylformamide; (2) the anhydride of carbobenzyloxyglycine is made as in (1) and reacted with dl-phenylalanine in aqueous sodium hydroxide to yield carbobenzyloxy-glycyl-dl-phenyl alanine; and in (3) and (4) methanol containing phenyltrimethylammonium methoxide is added respectively to carbobenzyloxyglycyl-dl- or l-phenylalanine in dimethylformamide, some solvent removed, sulphur trioxide in dimethylformamide added and then glycine in aqueous sodium hydroxide to yield the corresponding carbobenzyloxyglycyl - phenylalanylglycine. It is stated that the following compounds have been made: p-toluenesulphonyl-dl - alanylglycine, carbobenzyloxy - dl - alanylglycine, carbobenzyloxyglycyl-dl-phenylalanine, carbobenzyloxyglycyl - l - phenylalanine, carbobenzyloxy - l - phenylalanylglycine and p-toluenesulphonyl - glycyl - dl - phenylalanine.</abstract><oa>free_for_read</oa></addata></record>
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title Improvements in or relating to the manufacture of peptides, polypeptides and derivatives thereof
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