New amino-imidazole substituted amino acid derivatives

2-Amino-imidazol-4-yl N-(hetero)arylsulphonyl-amino acid amides (I), their stereoisomers, mixtures and salts are new: A = 1-6C alkylene; or 3-6C alkenylene with the double bond alpha to the imidazole ring; R1 = Ph optionally monosubstituted by alkyl, alkoxy, NMe2, NEt2, NO2, NH2, CN, CF3, F, Cl, Br...

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Hauptverfasser: GRELL, WOLFGANG. DR., 88400 BIBERACH, DE, BINDER, KLAUS-BIOL. DR., 65187 WIESBADEN, DE, WIENEN, WOLFGANG-BIOL. DR., 88400 BIBERACH, DE, HAAKSMA, ERIC., 88400 BIBERACH, DE, ZIMMERMANN, RAINER-BIO.. DR., 88441 MITTELBIBERACH, DE, HALLERMAYER, GERHARD. DR., 88437 MASELHEIM, DE
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creator GRELL, WOLFGANG. DR., 88400 BIBERACH, DE
BINDER, KLAUS-BIOL. DR., 65187 WIESBADEN, DE
WIENEN, WOLFGANG-BIOL. DR., 88400 BIBERACH, DE
HAAKSMA, ERIC., 88400 BIBERACH, DE
ZIMMERMANN, RAINER-BIO.. DR., 88441 MITTELBIBERACH, DE
HALLERMAYER, GERHARD. DR., 88437 MASELHEIM, DE
description 2-Amino-imidazol-4-yl N-(hetero)arylsulphonyl-amino acid amides (I), their stereoisomers, mixtures and salts are new: A = 1-6C alkylene; or 3-6C alkenylene with the double bond alpha to the imidazole ring; R1 = Ph optionally monosubstituted by alkyl, alkoxy, NMe2, NEt2, NO2, NH2, CN, CF3, F, Cl, Br or I; Ph disubstituted by alkyl or alkoxy; Ph substituted by 1 NH2 and 2 Cl or Br; 1- or 2-naphthyl optionally monosubstituted by alkyl, alkoxy, NMe2, NEt2 or Cl; 1- or 2-naphthyl disubstituted by alkyl or alkoxy; quinolin-8-yl or isoquinolin-5, -6- or -7-yl optionally monosubstituted by alkyl; isoindolin-5-yl-, 1,2,3,4-tetrahydroquinolin-8-yl, 1,2,3,4-tetrahydro-isoquinolin-5-, -6- or -7-yl or 2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl optionally monosubstituted by alkyl in the non-aromatic ring; 5,6,7,8-tetrahydro(1 or 2)naphthyl; anthracen-1-yl; anthraquinon-1-yl; 9H-fluoren-3-yl; dibenzofuran-2- or 4-yl; 9H-xanthen-2-yl; dibenzothiophen-2-yl; or phenoxathiin-2-yl; R2 = H; Me; or Y1-CO-1-3C alkyl; Y1 = OH; alkoxy; benzyloxy; NH2; NH(alkyl); or N(alkyl)2; R3 = H or Me; R4 = 1-6C alkyl; 3-6C alkenyl; 3-7C cycloalkyl; alkoxyalkyl; benzyl; tetrahydrofuran-2-ylmethyl; or tetrahydropyran-2-ylmethyl; R5 = H; 1-6C alkyl; 3-6C alkenyl; Y1-CO-1-3C alkyl; or (p-Y1-CO-C6H4)-1-3C alkyl; or NR4R5 = 4-6C alkyleneimino optionally monosubstituted by alkyl, alkoxy or W or disubstituted by alkyl and W; W = HOCH2-; alkoxy-CH2-; (alkyl or alkoxy)-CO-O-CH2-; H2N-CH2-; alkyl-NH-CH2-; benzyl-NH-CH2-; (alkyl, alkoxy or benzyloxy)-CO-NH-CH2-; (alkyl or benzyl)2N-CH2-; CN; 1H-tetrazol-5-yl; or Y2-CO-; Y2 = OH; alkoxy; NH2; NH(alkyl or benzyl); N(alkyl or benzyl)2; or (carboxyalkyl, alkoxycarbonyl or benzyloxycarbonylalkyl)amino; and unspecified alkyl and alkylene contain 1-4C.
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DR., 88437 MASELHEIM, DE</creatorcontrib><description>2-Amino-imidazol-4-yl N-(hetero)arylsulphonyl-amino acid amides (I), their stereoisomers, mixtures and salts are new: A = 1-6C alkylene; or 3-6C alkenylene with the double bond alpha to the imidazole ring; R1 = Ph optionally monosubstituted by alkyl, alkoxy, NMe2, NEt2, NO2, NH2, CN, CF3, F, Cl, Br or I; Ph disubstituted by alkyl or alkoxy; Ph substituted by 1 NH2 and 2 Cl or Br; 1- or 2-naphthyl optionally monosubstituted by alkyl, alkoxy, NMe2, NEt2 or Cl; 1- or 2-naphthyl disubstituted by alkyl or alkoxy; quinolin-8-yl or isoquinolin-5, -6- or -7-yl optionally monosubstituted by alkyl; isoindolin-5-yl-, 1,2,3,4-tetrahydroquinolin-8-yl, 1,2,3,4-tetrahydro-isoquinolin-5-, -6- or -7-yl or 2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl optionally monosubstituted by alkyl in the non-aromatic ring; 5,6,7,8-tetrahydro(1 or 2)naphthyl; anthracen-1-yl; anthraquinon-1-yl; 9H-fluoren-3-yl; dibenzofuran-2- or 4-yl; 9H-xanthen-2-yl; dibenzothiophen-2-yl; or phenoxathiin-2-yl; R2 = H; Me; or Y1-CO-1-3C alkyl; Y1 = OH; alkoxy; benzyloxy; NH2; NH(alkyl); or N(alkyl)2; R3 = H or Me; R4 = 1-6C alkyl; 3-6C alkenyl; 3-7C cycloalkyl; alkoxyalkyl; benzyl; tetrahydrofuran-2-ylmethyl; or tetrahydropyran-2-ylmethyl; R5 = H; 1-6C alkyl; 3-6C alkenyl; Y1-CO-1-3C alkyl; or (p-Y1-CO-C6H4)-1-3C alkyl; or NR4R5 = 4-6C alkyleneimino optionally monosubstituted by alkyl, alkoxy or W or disubstituted by alkyl and W; W = HOCH2-; alkoxy-CH2-; (alkyl or alkoxy)-CO-O-CH2-; H2N-CH2-; alkyl-NH-CH2-; benzyl-NH-CH2-; (alkyl, alkoxy or benzyloxy)-CO-NH-CH2-; (alkyl or benzyl)2N-CH2-; CN; 1H-tetrazol-5-yl; or Y2-CO-; Y2 = OH; alkoxy; NH2; NH(alkyl or benzyl); N(alkyl or benzyl)2; or (carboxyalkyl, alkoxycarbonyl or benzyloxycarbonylalkyl)amino; and unspecified alkyl and alkylene contain 1-4C.</description><edition>6</edition><language>eng ; ger</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1997</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=19970703&amp;DB=EPODOC&amp;CC=DE&amp;NR=19548797A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25543,76293</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19970703&amp;DB=EPODOC&amp;CC=DE&amp;NR=19548797A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>GRELL, WOLFGANG. DR., 88400 BIBERACH, DE</creatorcontrib><creatorcontrib>BINDER, KLAUS-BIOL. DR., 65187 WIESBADEN, DE</creatorcontrib><creatorcontrib>WIENEN, WOLFGANG-BIOL. DR., 88400 BIBERACH, DE</creatorcontrib><creatorcontrib>HAAKSMA, ERIC., 88400 BIBERACH, DE</creatorcontrib><creatorcontrib>ZIMMERMANN, RAINER-BIO.. DR., 88441 MITTELBIBERACH, DE</creatorcontrib><creatorcontrib>HALLERMAYER, GERHARD. DR., 88437 MASELHEIM, DE</creatorcontrib><title>New amino-imidazole substituted amino acid derivatives</title><description>2-Amino-imidazol-4-yl N-(hetero)arylsulphonyl-amino acid amides (I), their stereoisomers, mixtures and salts are new: A = 1-6C alkylene; or 3-6C alkenylene with the double bond alpha to the imidazole ring; R1 = Ph optionally monosubstituted by alkyl, alkoxy, NMe2, NEt2, NO2, NH2, CN, CF3, F, Cl, Br or I; Ph disubstituted by alkyl or alkoxy; Ph substituted by 1 NH2 and 2 Cl or Br; 1- or 2-naphthyl optionally monosubstituted by alkyl, alkoxy, NMe2, NEt2 or Cl; 1- or 2-naphthyl disubstituted by alkyl or alkoxy; quinolin-8-yl or isoquinolin-5, -6- or -7-yl optionally monosubstituted by alkyl; isoindolin-5-yl-, 1,2,3,4-tetrahydroquinolin-8-yl, 1,2,3,4-tetrahydro-isoquinolin-5-, -6- or -7-yl or 2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl optionally monosubstituted by alkyl in the non-aromatic ring; 5,6,7,8-tetrahydro(1 or 2)naphthyl; anthracen-1-yl; anthraquinon-1-yl; 9H-fluoren-3-yl; dibenzofuran-2- or 4-yl; 9H-xanthen-2-yl; dibenzothiophen-2-yl; or phenoxathiin-2-yl; R2 = H; Me; or Y1-CO-1-3C alkyl; Y1 = OH; alkoxy; benzyloxy; NH2; NH(alkyl); or N(alkyl)2; R3 = H or Me; R4 = 1-6C alkyl; 3-6C alkenyl; 3-7C cycloalkyl; alkoxyalkyl; benzyl; tetrahydrofuran-2-ylmethyl; or tetrahydropyran-2-ylmethyl; R5 = H; 1-6C alkyl; 3-6C alkenyl; Y1-CO-1-3C alkyl; or (p-Y1-CO-C6H4)-1-3C alkyl; or NR4R5 = 4-6C alkyleneimino optionally monosubstituted by alkyl, alkoxy or W or disubstituted by alkyl and W; W = HOCH2-; alkoxy-CH2-; (alkyl or alkoxy)-CO-O-CH2-; H2N-CH2-; alkyl-NH-CH2-; benzyl-NH-CH2-; (alkyl, alkoxy or benzyloxy)-CO-NH-CH2-; (alkyl or benzyl)2N-CH2-; CN; 1H-tetrazol-5-yl; or Y2-CO-; Y2 = OH; alkoxy; NH2; NH(alkyl or benzyl); N(alkyl or benzyl)2; or (carboxyalkyl, alkoxycarbonyl or benzyloxycarbonylalkyl)amino; and unspecified alkyl and alkylene contain 1-4C.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1997</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZDDzSy1XSMzNzMvXzczNTEmsys9JVSguTSouySwpLUlNgcgpJCZnpiikpBZlliWWZJalFvMwsKYl5hSn8kJpbgZFN9cQZw_d1IL8-NTigsTk1LzUkngXV0NLUxMLc0tzR0NjYtQAAMgTLgc</recordid><startdate>19970703</startdate><enddate>19970703</enddate><creator>GRELL, WOLFGANG. 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DR., 88437 MASELHEIM, DE</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_DE19548797A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; ger</language><creationdate>1997</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>GRELL, WOLFGANG. DR., 88400 BIBERACH, DE</creatorcontrib><creatorcontrib>BINDER, KLAUS-BIOL. DR., 65187 WIESBADEN, DE</creatorcontrib><creatorcontrib>WIENEN, WOLFGANG-BIOL. DR., 88400 BIBERACH, DE</creatorcontrib><creatorcontrib>HAAKSMA, ERIC., 88400 BIBERACH, DE</creatorcontrib><creatorcontrib>ZIMMERMANN, RAINER-BIO.. DR., 88441 MITTELBIBERACH, DE</creatorcontrib><creatorcontrib>HALLERMAYER, GERHARD. DR., 88437 MASELHEIM, DE</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>GRELL, WOLFGANG. DR., 88400 BIBERACH, DE</au><au>BINDER, KLAUS-BIOL. DR., 65187 WIESBADEN, DE</au><au>WIENEN, WOLFGANG-BIOL. DR., 88400 BIBERACH, DE</au><au>HAAKSMA, ERIC., 88400 BIBERACH, DE</au><au>ZIMMERMANN, RAINER-BIO.. DR., 88441 MITTELBIBERACH, DE</au><au>HALLERMAYER, GERHARD. DR., 88437 MASELHEIM, DE</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>New amino-imidazole substituted amino acid derivatives</title><date>1997-07-03</date><risdate>1997</risdate><abstract>2-Amino-imidazol-4-yl N-(hetero)arylsulphonyl-amino acid amides (I), their stereoisomers, mixtures and salts are new: A = 1-6C alkylene; or 3-6C alkenylene with the double bond alpha to the imidazole ring; R1 = Ph optionally monosubstituted by alkyl, alkoxy, NMe2, NEt2, NO2, NH2, CN, CF3, F, Cl, Br or I; Ph disubstituted by alkyl or alkoxy; Ph substituted by 1 NH2 and 2 Cl or Br; 1- or 2-naphthyl optionally monosubstituted by alkyl, alkoxy, NMe2, NEt2 or Cl; 1- or 2-naphthyl disubstituted by alkyl or alkoxy; quinolin-8-yl or isoquinolin-5, -6- or -7-yl optionally monosubstituted by alkyl; isoindolin-5-yl-, 1,2,3,4-tetrahydroquinolin-8-yl, 1,2,3,4-tetrahydro-isoquinolin-5-, -6- or -7-yl or 2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl optionally monosubstituted by alkyl in the non-aromatic ring; 5,6,7,8-tetrahydro(1 or 2)naphthyl; anthracen-1-yl; anthraquinon-1-yl; 9H-fluoren-3-yl; dibenzofuran-2- or 4-yl; 9H-xanthen-2-yl; dibenzothiophen-2-yl; or phenoxathiin-2-yl; R2 = H; Me; or Y1-CO-1-3C alkyl; Y1 = OH; alkoxy; benzyloxy; NH2; NH(alkyl); or N(alkyl)2; R3 = H or Me; R4 = 1-6C alkyl; 3-6C alkenyl; 3-7C cycloalkyl; alkoxyalkyl; benzyl; tetrahydrofuran-2-ylmethyl; or tetrahydropyran-2-ylmethyl; R5 = H; 1-6C alkyl; 3-6C alkenyl; Y1-CO-1-3C alkyl; or (p-Y1-CO-C6H4)-1-3C alkyl; or NR4R5 = 4-6C alkyleneimino optionally monosubstituted by alkyl, alkoxy or W or disubstituted by alkyl and W; W = HOCH2-; alkoxy-CH2-; (alkyl or alkoxy)-CO-O-CH2-; H2N-CH2-; alkyl-NH-CH2-; benzyl-NH-CH2-; (alkyl, alkoxy or benzyloxy)-CO-NH-CH2-; (alkyl or benzyl)2N-CH2-; CN; 1H-tetrazol-5-yl; or Y2-CO-; Y2 = OH; alkoxy; NH2; NH(alkyl or benzyl); N(alkyl or benzyl)2; or (carboxyalkyl, alkoxycarbonyl or benzyloxycarbonylalkyl)amino; and unspecified alkyl and alkylene contain 1-4C.</abstract><edition>6</edition><oa>free_for_read</oa></addata></record>
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METALLURGY
ORGANIC CHEMISTRY
title New amino-imidazole substituted amino acid derivatives
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