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公开(公告)号:DE3374004D1
公开(公告)日:1987-11-12
申请号:DE3374004
申请日:1983-12-13
Applicant: HOECHST AG
Inventor: URBACH HANSJORG DR , HENNING RAINER DR , TEETZ VOLKER DR , BECKER REINHARD DR
IPC: A61K31/40 , A61K31/403 , A61K38/00 , A61P9/12 , A61P43/00 , C07D209/52 , C07K1/113 , C07K5/02 , C07K5/06 , C07K14/81
Abstract: The invention relates to derivatives of cis,endo-2-azabicyclo[5.3.0]decane-3-carboxylic acid of the formula I (I) in which R denotes hydrogen, alkyl, alkenyl or aralkyl, R1 denotes hydrogen, allyl, vinyl or a side chain of an optionally protected naturally occurring alpha -aminoacid, R2 denotes hydrogen, alkyl, alkenyl or aralkyl, Y denotes hydrogen or hydroxyl, Z denotes hydrogen, or Y and Z together denote oxygen, X denotes alkyl, alkenyl, cycloalkyl, aryl which can be substituted once, twice or three times by alkyl, alkoxy, hydroxyl, halogen, nitro, amino, alkylamino, dialkylamino or methylenedioxy, or denotes indol-3-yl, and their physiologically acceptable salts, a process for their preparation, agents containing them and their use.
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公开(公告)号:DE3373818D1
公开(公告)日:1987-10-29
申请号:DE3373818
申请日:1983-11-07
Applicant: HOECHST AG
Inventor: URBACH HANSJORG DR , HENNING RAINER DR , BECKER REINHARD DR
IPC: C07D209/70 , A61K31/40 , A61K31/403 , A61K38/00 , A61K38/55 , A61P9/12 , A61P43/00 , C07D209/58 , C07D221/22 , C07K1/02 , C07K1/113 , C07K5/02 , C07K5/06 , C07K14/81 , A61K37/02
Abstract: The invention relates to new derivatives of tricyclic aminoacids, of the formula I (I) in which n denotes 0 or 1, A denotes -CH=CH- or -CH2-CH2-, R denotes hydrogen, alkyl or aralkyl, R1 denotes hydrogen, or alkyl, which can optionally be substituted by amino, acylamino or benzoylamino, or alkenyl, cycloalkyl, cycloalkenyl, cycloalkylalkyl, aryl or partially hydrogenated aryl, each of which can be substituted by alkyl, alkoxy or halogen, or aralkyl or aroylalkyl, both of which can be substituted as defined above, or a monocyclic or bicyclic S-, O- and/or N-heterocyclene radical, or a side chain of a naturally occurring aminoacid, which may be protected, R2 denotes hydrogen, alkyl, alkenyl or aralkyl, Y denotes hydrogen or hydroxyl and Z denotes hydrogen, or Y and Z together denote oxygen, and X denotes alkyl, alkenyl, cycloalkyl, aryl, which can be mono-, di- or tri-substituted by alkyl, alkoxy, hydroxyl, halogen, nitro, amino, alkylamino, dialkylamino and/or methylenedioxy, or 3-indolyl, and physiologically acceptable salts thereof, processes for their preparation, agents containing these compounds and their use, and new bicyclic aminoacids as intermediates and processes for their preparation.
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公开(公告)号:AT28565T
公开(公告)日:1987-08-15
申请号:AT83102868
申请日:1983-03-23
Applicant: HOECHST AG
Inventor: TEETZ VOLKER DR , URBACH HANSJOERG DR , BECKER REINHARD DR
IPC: A61K31/40 , A61K31/403 , A61K38/00 , A61P9/12 , C07D209/54 , C07K1/113 , C07K5/02 , C07K5/06 , A61K37/02
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公开(公告)号:DE3537460A1
公开(公告)日:1987-04-23
申请号:DE3537460
申请日:1985-10-22
Applicant: HOECHST AG
Inventor: URBACH HANSJOERG DR , HENNING RAINER DR , BECKER REINHARD DR
Abstract: The invention relates to derivatives of bicyclic amino acids of the formula I in which n is 0, 1 or 2 and R, R , R and X have the stated meaning, to process for their preparation, to compositions containing these and to their use.
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公开(公告)号:GR82242B
公开(公告)日:1984-12-13
申请号:GR840175221
申请日:1984-07-05
Applicant: HOECHST AG
Inventor: URBACH HANSJORG DR , HENNING RAINER DR , BECKER REINHARD DR
IPC: A61K31/40 , A61K31/403 , A61K31/405 , A61K38/00 , A61K38/55 , A61P9/12 , A61P43/00 , C07D209/52 , C07D221/04 , C07K1/113 , C07K5/02 , C07K5/06 , C07K5/08 , C07K14/81
Abstract: The invention relates to compounds of the formula I (I) in which n denotes 0 or 1, R denotes hydrogen, alkyl, alkenyl or aralkyl, R1 denotes hydrogen or alkyl, which can optionally be substituted by amino, acylamino or benzoylamino, alkenyl, cycloalkyl, cycloalkenyl, cycloalkylalkyl, aryl or partially hydrogenated aryl, each of which can be substituted by alkyl, alkoxy or halogen, aralkyl or aroylalkyl, both of which can be substituted in the aryl radical as defined previously, a monocyclic or bicyclic S- or O- and/or N-heterocyclic radical or a side chain of an aminoacid, R2 denotes hydrogen, alkyl, alkenyl or aralkyl, Y denotes hydrogen or hydroxyl, Z denotes hydrogen, or Y and Z together denote oxygen, X denotes alkyl, alkenyl, cycloalkyl, aryl, which can be monosubstituted, disubstituted or trisubstituted by alkyl, alkoxy, hydroxyl, halogen, nitro, amino, acylamino, alkylamino, dialkylamino and/or methylenedioxy, or 3-indolyl, and to a process for their preparation, agents containing them and and their use, and to 2-azabicyclo[3.1.0]hexane derivatives as intermediates, and a process for their preparation.
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公开(公告)号:GR78496B
公开(公告)日:1984-09-27
申请号:GR830170883
申请日:1983-03-23
Applicant: HOECHST AG
Inventor: TEETZ VOLKER DR , HANSJORGURBACH DR , BECKER REINHARD DR
IPC: A61K31/40 , A61K31/403 , A61K38/00 , A61P9/12 , C07D209/54 , C07K1/113 , C07K5/02 , C07K5/06
Abstract: The invention relates to compounds of the formula I (I) in which n denotes 1, 2, 3 or 4, R is alkyl, alkenyl cycloalkyl, aryl, optionally mono-, di- oder trisubstituted by alkyl, alkoxy, hydroxy, halogen, nitro, amino, alkylamino, dialkylamino or methylenedioxy, or indol-3-yl, R1 denotes an optionally protected radical of a naturally occurring amino acid HOOC-CH(NH2)-R1, R2 denotes hydrogen, alkyl or optionally nitro-substituted aralkyl, R3 denotes hydrogen, alkyl or cycloalkyl or optionally nitro-substituted aralkyl and X denotes 2 hydrogen atoms or 1 oxygen atom, their physiologically tolerated salts with acids and, if R2 and/or R3 denote hydrogen, with bases, a process for their preparation, agents containing these derivatives and their use as medicaments.
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公开(公告)号:DE3300774A1
公开(公告)日:1984-07-12
申请号:DE3300774
申请日:1983-01-12
Applicant: HOECHST AG
Inventor: HENNING RAINER DR , URBACH HANSJOERG DR , TEETZ VOLKER DR , BECKER REINHARD DR
IPC: A61K38/00 , A61K38/55 , A61P9/12 , A61P43/00 , C07D209/96 , C07D317/28 , C07D317/30 , C07D317/32 , C07D317/72 , C07K1/02 , C07K1/113 , C07K5/02 , C07K5/06 , C07K5/078 , C07K14/81 , C07D209/54 , C07D401/06 , C07D403/06 , C07D405/06 , C07D473/00 , C07D455/02 , C07D475/00 , C07D413/06 , C07D417/06 , A61K31/40 , A61K31/195
Abstract: The invention relates to new spirocyclic aminoacid derivatives of the formula I (I) in which m denotes 1 or 2, n denotes 0 or 1, R denotes hydrogen, alkyl or aralkyl, R1 denotes hydrogen or alkyl which can be optionally substituted by amino, acylamino or benzoylamino, alkenyl, cycloalkyl, cycloalkenyl, cycloalkylalkyl, aryl or partially hydrogenated aryl, each of which can be substituted by alkyl, alkoxy or halogen, arylalkyl or aroylalkyl, both of which can be substituted as defined above in the aryl radical, an S- or O- and/or N-heterocyclic radical or a side chain of an alpha -aminoacid, R2 denotes hydrogen, alkyl, alkenyl or aralkyl, Y denotes hydrogen or hydroxyl, Z denotes hydrogen, or Y and Z together denote oxygen and X denotes alkyl, alkenyl, cycloalkyl, aryl, which can be monosubstituted, disubstituted or trisubstituted by alkyl, alkoxy, hydroxyl, halogen, nitro, amino, alkylamino, dialkylamino and/or methylenedioxy, or 3-indolyl, processes for their preparation, agents containing them and their use and new spirocyclic aminoacids as intermediates and a process for their preparation.
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公开(公告)号:DE3246503A1
公开(公告)日:1984-06-20
申请号:DE3246503
申请日:1982-12-16
Applicant: HOECHST AG
Inventor: URBACH HANSJOERG DR , HENNING RAINER DR , TEETZ VOLKER DR , BECKER REINHARD DR
IPC: A61K31/40 , A61K31/403 , A61K38/00 , A61P9/12 , A61P43/00 , C07D209/52 , C07K1/113 , C07K5/02 , C07K5/06 , C07K14/81
Abstract: The invention relates to derivatives of cis,endo-2-azabicyclo[5.3.0]decane-3-carboxylic acid of the formula I (I) in which R denotes hydrogen, alkyl, alkenyl or aralkyl, R1 denotes hydrogen, allyl, vinyl or a side chain of an optionally protected naturally occurring alpha -aminoacid, R2 denotes hydrogen, alkyl, alkenyl or aralkyl, Y denotes hydrogen or hydroxyl, Z denotes hydrogen, or Y and Z together denote oxygen, X denotes alkyl, alkenyl, cycloalkyl, aryl which can be substituted once, twice or three times by alkyl, alkoxy, hydroxyl, halogen, nitro, amino, alkylamino, dialkylamino or methylenedioxy, or denotes indol-3-yl, and their physiologically acceptable salts, a process for their preparation, agents containing them and their use.
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公开(公告)号:DE3227055A1
公开(公告)日:1984-01-26
申请号:DE3227055
申请日:1982-07-20
Applicant: HOECHST AG
Inventor: HENNING RAINER DR , URBACH HANSJOERG DR , BECKER REINHARD DR
IPC: A61K31/435 , A61K38/00 , A61P9/12 , C07D453/06 , C07K5/02 , A61K45/06
Abstract: The novel derivatives have the formula I in which n denotes 0 or 2, R denotes hydrogen, alkyl or aralkyl, R denotes hydrogen or unsubstituted or amino-, acylamino- or benzoylamino-substituted alkyl, alkenyl, cycloalkyl, cycloalkenyl, cycloalkylalkyl, aryl or partially hydrogenated aryl, each of which can be substituted by alkyl, alkoxy or halogen, aralkyl or aroylalkyl, both of which, as defined above, can be substituted in the aryl radical, an S- or O- and/or N-heterocyclic radical or a side chain of an amino acid, R denotes hydrogen, alkyl, alkenyl or aralkyl, Y denotes hydrogen or hydroxyl, Z denotes hydrogen or Y and Z together denote oxygen and X denotes alkyl, alkenyl, cycloalkyl, aryl, which can be mono-, di- or trisubstituted by alkyl, alkoxy, hydroxyl, halogen, nitro, amino, alkylamino, dialkylamino and/or methylenedioxy or denotes 3-indolyl.
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公开(公告)号:DE3210496A1
公开(公告)日:1983-10-06
申请号:DE3210496
申请日:1982-03-23
Applicant: HOECHST AG
Inventor: URBACH HANSJOERG DR , HENNING RAINER DR , TEETZ VOLKER DR , WISSMANN HANS DR , BECKER REINHARD DR
IPC: A61K31/40 , A61K31/403 , A61K31/404 , A61K31/405 , A61K38/00 , A61K38/55 , A61P9/12 , C07D209/42 , C07K1/02 , C07K1/113 , C07K5/02 , C07K5/06 , C07K14/81 , C07D401/06 , C07D401/14 , C07D403/06 , C07D403/14 , C07D405/06 , C07D405/14 , C07D209/26
Abstract: The invention relates to compounds of the formula I (I) in which n denotes 0 or 1, R denotes hydrogen, alkyl or aralky, R1 denotes hydrogen or alkyl, which can optionally be substituted by amino, acylamino or benzoylamino, alkenyl, cycloalkyl, cycloalkenyl, cycloalkylalkyl, aryl or partially hydrogenated aryl, which each can be substituted by alkyl, alkoxy or halogen, arylalkyl or aroylalkyl, both of which can be substituted in the aryl radical as defined in the aforegoing, a monocyclic or bicyclic sulfur or oxygen and/or nitrogen heterocyclic radical, or a side chain of a naturally occurring aminoacid, R2 denotes hydrogen, alkyl, alkenyl or arylalkyl, Y denotes hydrogen or hydroxyl, Z denotes hydrogen or Y and Z together denote oxygen and X denotes alkyl, alkenyl, cycloalkyl, aryl, which is monosubstituted, disubstituted or trisubstituted by alkyl, alkoxy, hydroxyl, halogen, nitro, amino, alkylamino, dialkylamino or methylenedioxy or 3-indolyl, and their physiologically acceptable salts, processes for their preparation, agents containing these and their use as medicaments and also bicyclic amino acids as their intermediates and processes for their preparation.
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