-
21.Processes and intermediates for manufacturing retroviral protease inhibiting compounds 失效
Title translation: 方法和中间体逆转录病毒蛋白酶抑制剂的制备中公开(公告)号:EP1302468B1
公开(公告)日:2008-12-17
申请号:EP02079949.0
申请日:1993-12-16
Applicant: ABBOTT LABORATORIES
Inventor: Kempf, Dale J. , Norbeck, Daniel W. , Sham, Hing Leung , Zhao, Chen , Sowin, Thomas J. , Reno, Daniel S. , Haight, Anthony R. , Cooper, Arthur J.
IPC: C07D277/24 , C07D277/28 , C07D303/36 , C07D277/34 , C07D277/42 , C07D417/12 , C07D263/32 , C07D413/12 , C07F5/02 , A61K31/426 , A61P31/18
CPC classification number: C07D413/12 , A61K31/425 , A61K31/427 , A61K31/70 , A61K38/00 , A61K45/06 , C07C33/46 , C07C43/164 , C07C43/1742 , C07C43/2055 , C07C43/215 , C07C43/23 , C07C43/30 , C07C43/315 , C07C45/004 , C07C45/29 , C07C45/567 , C07C45/62 , C07C45/673 , C07C45/74 , C07C53/134 , C07C69/34 , C07C69/65 , C07C69/732 , C07C211/27 , C07C215/18 , C07C215/20 , C07C215/28 , C07C229/08 , C07C229/26 , C07C229/34 , C07C233/36 , C07C233/40 , C07C235/10 , C07C235/12 , C07C235/34 , C07C235/78 , C07C237/10 , C07C237/20 , C07C237/22 , C07C239/10 , C07C239/18 , C07C239/20 , C07C247/10 , C07C251/40 , C07C271/20 , C07C271/22 , C07C271/34 , C07C275/16 , C07C275/24 , C07C311/03 , C07C311/13 , C07C311/18 , C07C317/10 , C07C317/28 , C07C317/44 , C07C323/12 , C07C323/25 , C07C381/00 , C07D213/26 , C07D213/30 , C07D213/34 , C07D213/40 , C07D213/54 , C07D213/56 , C07D213/61 , C07D213/75 , C07D231/12 , C07D233/56 , C07D233/64 , C07D233/84 , C07D235/14 , C07D235/16 , C07D239/26 , C07D241/12 , C07D249/08 , C07D261/08 , C07D263/32 , C07D277/24 , C07D277/28 , C07D277/30 , C07D277/34 , C07D277/36 , C07D277/40 , C07D277/42 , C07D277/56 , C07D295/13 , C07D295/205 , C07D295/215 , C07D303/36 , C07D307/42 , C07D333/16 , C07D401/12 , C07D417/12 , C07K5/06026 , C07K5/06078 , A61K31/00 , A61K2300/00 , C07C49/233 , C07C49/255 , C07C49/215 , C07C49/245 , C07C49/235 , C07C49/223
Abstract: A retroviral protease inhibiting compound of formula (A) is disclosed for use in combination with other active pharmaceutical agents for treating a human infected by HIV. Intermediates and processes useful in the manufacture of compounds of formula (A) are also disclosed.
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22.Intermediates for preparating non-peptide retroviral protease inhibitors 失效
Title translation: Zvischenprodukte zur Herstellung von non-peptiden retroviralproteasehemmenden Verbindungen公开(公告)号:EP0839798B1
公开(公告)日:2005-08-17
申请号:EP97119700.9
申请日:1990-05-17
Applicant: ABBOTT LABORATORIES
Inventor: Kempf, Dale J. , Norbeck, Daniel W. , Erickson, John W. , Sham, Hing Leung , Codacovi, Lynn M. , Plattner, Jacob J.
IPC: C07C215/18 , C07C271/20 , C07C237/10 , C07D303/40 , C07D303/46
CPC classification number: C07D207/08 , A61K38/00 , C07C33/46 , C07C43/164 , C07C43/1742 , C07C43/2055 , C07C43/215 , C07C43/23 , C07C43/30 , C07C43/315 , C07C45/004 , C07C45/29 , C07C45/567 , C07C45/59 , C07C45/62 , C07C45/673 , C07C45/74 , C07C53/134 , C07C69/34 , C07C69/65 , C07C69/732 , C07C211/27 , C07C215/18 , C07C215/20 , C07C215/28 , C07C229/08 , C07C229/26 , C07C229/34 , C07C233/36 , C07C233/40 , C07C235/10 , C07C235/12 , C07C235/34 , C07C235/78 , C07C237/10 , C07C237/20 , C07C237/22 , C07C239/10 , C07C239/18 , C07C239/20 , C07C247/10 , C07C251/40 , C07C271/20 , C07C271/22 , C07C271/34 , C07C275/16 , C07C275/24 , C07C311/03 , C07C311/13 , C07C311/18 , C07C317/10 , C07C317/28 , C07C317/44 , C07C323/12 , C07C323/25 , C07C381/00 , C07C2601/14 , C07D207/24 , C07D209/42 , C07D211/62 , C07D213/30 , C07D213/40 , C07D213/42 , C07D213/56 , C07D213/70 , C07D213/81 , C07D213/82 , C07D215/16 , C07D217/16 , C07D217/26 , C07D231/12 , C07D233/56 , C07D233/84 , C07D239/38 , C07D249/08 , C07D263/32 , C07D277/24 , C07D277/28 , C07D277/36 , C07D277/42 , C07D277/56 , C07D295/088 , C07D295/15 , C07D295/155 , C07D295/185 , C07D295/205 , C07D295/215 , C07D295/26 , C07D303/04 , C07D303/22 , C07D303/36 , C07D303/48 , C07D307/42 , C07D317/12 , C07D413/12 , C07D417/12 , C07D487/04 , C07F9/3241 , C07F9/5333 , C07K5/021 , C07K5/06043 , C07K5/06052 , C07K5/06139 , Y02P20/55 , C07C49/233 , C07C49/255 , C07C49/215 , C07C49/245 , C07C49/235 , C07C49/223
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公开(公告)号:EP1090914B1
公开(公告)日:2003-01-02
申请号:EP00124382.3
申请日:1993-12-16
Applicant: ABBOTT LABORATORIES
Inventor: Kempf, Dale J. , Norbeck, Daniel W. , Sham, Hing Leung , Zhao, Chen , Sowin, Thomas J. , Reno, Daniel S. , Haight, Anthony R. , Cooper, Arthur J.
IPC: C07D277/24 , C07D277/28 , C07D303/36 , C07D277/34 , C07D277/42 , C07D417/12 , C07D263/32 , C07D413/12 , C07F5/02 , A61K31/426 , A61P31/18
CPC classification number: C07D413/12 , A61K31/425 , A61K31/427 , A61K31/70 , A61K38/00 , A61K45/06 , C07C33/46 , C07C43/164 , C07C43/1742 , C07C43/2055 , C07C43/215 , C07C43/23 , C07C43/30 , C07C43/315 , C07C45/004 , C07C45/29 , C07C45/567 , C07C45/62 , C07C45/673 , C07C45/74 , C07C53/134 , C07C69/34 , C07C69/65 , C07C69/732 , C07C211/27 , C07C215/18 , C07C215/20 , C07C215/28 , C07C229/08 , C07C229/26 , C07C229/34 , C07C233/36 , C07C233/40 , C07C235/10 , C07C235/12 , C07C235/34 , C07C235/78 , C07C237/10 , C07C237/20 , C07C237/22 , C07C239/10 , C07C239/18 , C07C239/20 , C07C247/10 , C07C251/40 , C07C271/20 , C07C271/22 , C07C271/34 , C07C275/16 , C07C275/24 , C07C311/03 , C07C311/13 , C07C311/18 , C07C317/10 , C07C317/28 , C07C317/44 , C07C323/12 , C07C323/25 , C07C381/00 , C07D213/26 , C07D213/30 , C07D213/34 , C07D213/40 , C07D213/54 , C07D213/56 , C07D213/61 , C07D213/75 , C07D231/12 , C07D233/56 , C07D233/64 , C07D233/84 , C07D235/14 , C07D235/16 , C07D239/26 , C07D241/12 , C07D249/08 , C07D261/08 , C07D263/32 , C07D277/24 , C07D277/28 , C07D277/30 , C07D277/34 , C07D277/36 , C07D277/40 , C07D277/42 , C07D277/56 , C07D295/13 , C07D295/205 , C07D295/215 , C07D303/36 , C07D307/42 , C07D333/16 , C07D401/12 , C07D417/12 , C07K5/06026 , C07K5/06078 , A61K31/00 , A61K2300/00 , C07C49/233 , C07C49/255 , C07C49/215 , C07C49/245 , C07C49/235 , C07C49/223
Abstract: A retroviral protease inhibiting compound of formula (A) is disclosed for use in combination with other active pharmaceutical agents for treating a human infected by HIV. Intermediates and processes useful in the manufacture of compounds of formula (A) are also disclosed.
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24.Processes and intermediates for manufacturing retroviral protease inhibiting compounds 失效
Title translation: 方法和中间体逆转录病毒蛋白酶抑制剂的制备中公开(公告)号:EP1090914A2
公开(公告)日:2001-04-11
申请号:EP00124382.3
申请日:1993-12-16
Applicant: ABBOTT LABORATORIES
Inventor: Kempf, Dale J. , Norbeck, Daniel W. , Sham, Hing Leung , Zhao, Chen , Sowin, Thomas J. , Reno, Daniel S. , Haight, Anthony R. , Cooper, Arthur J.
IPC: C07D277/24 , C07D277/28 , C07D303/36 , C07D277/34 , C07D277/42 , C07D417/12 , C07D263/32 , C07D413/12 , C07F5/02 , A61K31/426 , A61P31/18
CPC classification number: C07D413/12 , A61K31/425 , A61K31/427 , A61K31/70 , A61K38/00 , A61K45/06 , C07C33/46 , C07C43/164 , C07C43/1742 , C07C43/2055 , C07C43/215 , C07C43/23 , C07C43/30 , C07C43/315 , C07C45/004 , C07C45/29 , C07C45/567 , C07C45/62 , C07C45/673 , C07C45/74 , C07C53/134 , C07C69/34 , C07C69/65 , C07C69/732 , C07C211/27 , C07C215/18 , C07C215/20 , C07C215/28 , C07C229/08 , C07C229/26 , C07C229/34 , C07C233/36 , C07C233/40 , C07C235/10 , C07C235/12 , C07C235/34 , C07C235/78 , C07C237/10 , C07C237/20 , C07C237/22 , C07C239/10 , C07C239/18 , C07C239/20 , C07C247/10 , C07C251/40 , C07C271/20 , C07C271/22 , C07C271/34 , C07C275/16 , C07C275/24 , C07C311/03 , C07C311/13 , C07C311/18 , C07C317/10 , C07C317/28 , C07C317/44 , C07C323/12 , C07C323/25 , C07C381/00 , C07D213/26 , C07D213/30 , C07D213/34 , C07D213/40 , C07D213/54 , C07D213/56 , C07D213/61 , C07D213/75 , C07D231/12 , C07D233/56 , C07D233/64 , C07D233/84 , C07D235/14 , C07D235/16 , C07D239/26 , C07D241/12 , C07D249/08 , C07D261/08 , C07D263/32 , C07D277/24 , C07D277/28 , C07D277/30 , C07D277/34 , C07D277/36 , C07D277/40 , C07D277/42 , C07D277/56 , C07D295/13 , C07D295/205 , C07D295/215 , C07D303/36 , C07D307/42 , C07D333/16 , C07D401/12 , C07D417/12 , C07K5/06026 , C07K5/06078 , A61K31/00 , A61K2300/00 , C07C49/233 , C07C49/255 , C07C49/215 , C07C49/245 , C07C49/235 , C07C49/223
Abstract: A retroviral protease inhibiting compound of formula (A) is disclosed for use in combination with other active pharmaceutical agents for treating a human infected by HIV. Intermediates and processes useful in the manufacture of compounds of formula (A) are also disclosed.
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25.Intermediates for preparating non-peptide retroviral protease inhibitors 失效
Title translation: 用于制备非肽逆转录病毒蛋白酶抑制剂的中间体公开(公告)号:EP0839798A3
公开(公告)日:1998-10-28
申请号:EP97119700.9
申请日:1990-05-17
Applicant: ABBOTT LABORATORIES
Inventor: Kempf, Dale J. , Norbeck, Daniel W. , Erickson, John W. , Sham, Hing Leung , Codacovi, Lynn M. , Plattner, Jacob J.
IPC: C07C215/18 , C07C271/20 , C07C237/10 , C07D303/40 , C07D303/46
Abstract: Intermediates, for preparing non-peptide retroviral protease inhibitors, said intermediates having the formula:
or an acid addition salt thereof or an N-protected derivative thereof wherein at each occurrence the N-protecting group is independently selected from the group consisting of formyl, acetyl, pivaloyl, t-butylacetyl, t-butyloxycarbonyl, benzyloxycarbonyl, benzyl and isopropylaminocarbonyl; or said intermediates being selected from:
(2S,3R,4S,5S)-2,5-di-(N-(Cbz-valinyl)amino)-3,4-dihydroxy-1,6-diphenylhexane; (2S,3S,4S,5S)-2,5-di-(N-(Cbz-valinyl)amino)-3,4-dihydroxy-1,6-diphenylhexane; (2S,3R,4R,5S)-2,5-di-(N-(Cbz-valinyl)amino)-3,4-dihydroxy-1,6-diphenylhexane; (2S,3S,4S,5S)-2,5-di-(N-(valinyl)amino)-3,4-dihydroxy-1,6-diphenylhexane; (2S,3R,4S,5S)-2,5-di-(N-(valinyl)amino)-3,4-dihydroxy-1,6-diphenylhexane; (2S,3R,4R,5S)-2,5-di-(N-(valinyl)amino)-3,4-dihydroxy-1,6-diphenylhexane; (2S,3S,4R,5S)-2-(N-(t-butyloxy)carbonyl)amino)-5-(N-(Cbz-valinyl)amino)-3,4-dihydroxy-1,6-diphenylhexane; 2-(N-benzyl-N-(benzyloxycarbonyl)amino)-5-(t-butyloxycarbonylamino)-1,6-diphenyl-3-hexene-3,4-oxide; 2-amino-5-(t-butyloxycarbonylamino)-1,6-diphenyl-3-hexene-3,4-oxide; and 2,5-di-(t-butyloxycarbonylamino)-1,6-diphenyl-3-hexene-3,4-oxide;
or an acid addition salt thereof.Abstract translation: 用于制备非肽逆转录病毒蛋白酶抑制剂的中间体,所述中间体具有下式:或其酸加成盐或其N-保护的衍生物,其中在每次出现时N-保护基独立地选自甲酰基,乙酰基 ,新戊酰基,叔丁基乙酰基,叔丁氧基羰基,苄氧基羰基,苄基和异丙基氨基羰基; 或所述中间体选自:(2S,3R,4S,5S)-2,5-二 - (N-(Cbz-缬氨酰基)氨基)-3,4-二羟基-1,6-二苯基己烷; (2S,3S,4S,5S)-2,5-二 - (N-(Cbz基缬氨酰)氨基)-3,4-二羟基-1,6-二苯基己烷; (2S,3R,4R,5S)-2,5-二 - (N-(Cbz基缬氨酰)氨基)-3,4-二羟基-1,6-二苯基己烷; (2S,3S,4S,5S)-2,5-二 - (N-(缬氨酰基)氨基)-3,4-二羟基-1,6-二苯基己烷; (2S,3R,4S,5S)-2,5-二 - (N-(缬氨酰基)氨基)-3,4-二羟基-1,6-二苯基己烷; (2S,3R,4R,5S)-2,5-二 - (N-(缬氨酰基)氨基)-3,4-二羟基-1,6-二苯基己烷; (2S,3S,4R,5S)-2-(N-(叔丁氧基)羰基)氨基)-5-(N-(Cbz基缬氨酰)氨基)-3,4-二羟基-1,6-二苯基己烷; 2-(N-苄基-N-(苄氧羰基)氨基)-5-(叔丁氧羰)-1,6-二苯基 - 3-己烯-3,4-氧化物; 2-氨基-5-(叔丁氧羰)-1,6-二苯基 - 3-己烯-3,4-氧化物; 和2,5-二 - (叔丁氧基羰基氨基)-1,6-二苯基-3-己烯-3,4-氧化物; 或其酸加成盐。
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公开(公告)号:EP0486948A3
公开(公告)日:1993-08-25
申请号:EP91119464.5
申请日:1991-11-04
Applicant: ABBOTT LABORATORIES
Inventor: Kempf, Dale J. , Codacovi, Lynn M. , Norbeck, Daniel W. , Plattner, Jacob J. , Sham, Hing L. , Wittenberger, Steven J. , Zhao, Chen
IPC: C07D213/26 , C07D213/30 , C07D213/40 , C07K5/06 , A61K37/64 , C07D213/56 , C07D211/16 , C07D295/20 , C07D277/30 , C07D277/42 , C07D417/12 , C07D277/40 , C07D401/12 , C07D277/24 , C07D277/28 , C07D235/14 , C07D235/16
CPC classification number: C07D213/30 , A61K38/00 , C07C53/134 , C07C215/18 , C07C215/20 , C07C215/28 , C07C233/40 , C07C237/10 , C07C237/22 , C07C271/20 , C07C271/22 , C07C271/34 , C07C275/24 , C07D213/26 , C07D213/34 , C07D213/40 , C07D213/54 , C07D213/56 , C07D213/61 , C07D213/75 , C07D231/12 , C07D233/56 , C07D233/64 , C07D233/84 , C07D235/14 , C07D235/16 , C07D239/26 , C07D241/12 , C07D249/08 , C07D261/08 , C07D263/32 , C07D277/24 , C07D277/28 , C07D277/30 , C07D277/36 , C07D277/40 , C07D277/42 , C07D277/56 , C07D295/13 , C07D295/205 , C07D295/215 , C07D303/36 , C07D307/42 , C07D333/16 , C07D401/12 , C07D413/10 , C07D417/12 , C07K5/06026 , C07K5/06078
Abstract: A retroviral protease inhibiting compound of the formula A -X- B is disclosed. Also disclosed are a composition and method for inhibiting a retroviral protease and for treating an HIV infection. Also disclosed are processes and intermediates useful for the preparation of the retroviral protease inhibitors.
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公开(公告)号:EP0307837A3
公开(公告)日:1991-12-11
申请号:EP88114867.0
申请日:1988-09-12
Applicant: ABBOTT LABORATORIES
Inventor: Rosenberg, Saul Howard , Sham, Hing Leung , Baker, William R. , Dellaria, Joseph F., Jr. , Kempf, Dale J.
IPC: C07D521/00 , A61K31/33 , C07K5/06 , C07K5/02 , A61K37/64
CPC classification number: C07D213/40 , A61K38/00 , C07C215/10 , C07C215/20 , C07C217/08 , C07C229/36 , C07C233/11 , C07C233/22 , C07C233/40 , C07C233/47 , C07C233/51 , C07C239/20 , C07C265/04 , C07C271/16 , C07C271/20 , C07C271/22 , C07C275/24 , C07C317/28 , C07C317/44 , C07C317/48 , C07C323/56 , C07C323/59 , C07C2601/08 , C07C2601/14 , C07D207/12 , C07D211/76 , C07D231/12 , C07D233/32 , C07D233/56 , C07D249/08 , C07D263/04 , C07D263/06 , C07D263/16 , C07D263/22 , C07D263/28 , C07D277/24 , C07D285/10 , C07D295/13 , C07D295/185 , C07D295/205 , C07D295/215 , C07D309/14 , C07D319/06 , C07D413/06 , C07K5/0227 , C07K5/06078
Abstract: A renin inhibiting compound of the formula:
wherein A is a substituent; W is C=O, CHOH or NR₂ wherein R₂ is hydrogen or loweralkyl; U is C=O, CH₂ or NR₂ wherein R₂ is hydrogen or loweralkyl, with the proviso that when W is CHOH then U is CH₂ and with the proviso that U is C=O or CH₂ when W is NR₂; V is CH, C(OH) or C(halogen) with the proviso that V is CH when U is NR₂; R₁ is loweralkyl, cycloalkylalkyl, benzyl, (alpha, alpha)-dimethylbenzyl, 4-methoxybenzyl, halobenzyl, 4-hydroxybenzyl, (1-naphthyl)methyl, (2-naphthyl)methyl, (unsubstituted heterocyclic)methyl, (substituted heterocyclic)methyl, phenethyl, 1-benzyloxyethyl, phenoxy, thiophenoxy or anilino, provided that B is CH₂ or CHOH or A is hydrogen when R₁ is phenoxy, thiophenoxy or anilino; R₃ is loweralkyl, loweralkenyl, ((alkoxy)alkoxy)alkyl, carboxyalkyl, (thioalkoxy)alkyl, azidoalkyl, aminoalkyl, (alkyl)aminoalkyl, dialkylaminoalkyl, (alkoxy)(alkyl)aminoalkyl, (alkoxy)aminoalkyl, benzyl or heterocyclic ring substituted methyl; R₄ is loweralkyl, cycloalkylmethyl or benzyl; R₅ is OH or NH₂; and Z is a substituent. Also disclosed are compositions for and a method of treating hypertension, methods of making the renin inhibiting compounds and intermediates useful in making the renin inhibiting compounds.Abstract translation: 一种下列化学式的肾素抑制化合物:其中A为取代基的
W是C = O,CHOH或NR2,其中R2是氢或低级烷基; U是C = O,CH 2或NR 2,其中R 2是氢或低级烷基,条件是当W是CHOH时,则U是CH 2,条件是当W是NR 2时,U是C = O或CH 2; V是CH,C(OH)或C(卤素),条件是当U是NR 2时,V是CH; R 1是低级烷基,环烷基烷基,苄基,(α,α) - 二甲基苄基,4-甲氧基苄基,卤代苄基,4-羟基苄基,(1-萘基)甲基,(2-萘基)甲基,(未取代的杂环)甲基,(取代的杂环) 甲基,苯乙基,1-苄氧基乙基,苯氧基,硫代苯氧基或苯胺基,条件是当R 1为苯氧基,苯硫基或苯胺基时,B为CH 2或CHOH或A为氢; R3是低级烷基,低级烯基,((烷氧基)烷氧基)烷基,羧基烷基,(硫代烷氧基)烷基,叠氮基烷基,氨基烷基,(烷基)氨基烷基,二烷基氨基烷基,(烷氧基)(烷基)氨基烷基,(烷氧基)氨基烷基,苄基或杂环取代 甲基; R4是低级烷基,环烷基甲基或苄基; R5是OH或NH2; Z为取代基。 还公开了治疗高血压的组合物和方法,制备肾素抑制化合物的方法和可用于制备肾素抑制化合物的中间体。 -
公开(公告)号:EP0342541A3
公开(公告)日:1991-11-06
申请号:EP89108590.4
申请日:1989-05-12
Applicant: ABBOTT LABORATORIES
Inventor: Kempf, Dale J. , Plattner, Jacob J. , Norbeck, Daniel W. , Baker, William R. , Fung, Anthony K. L. , Boyd, Steven A. , Erickson, John W. , Crowley, Steven R.
IPC: C07K5/02 , C07K5/04 , A61K37/64 , C07C103/49 , C07D307/22 , C07C125/065 , C07D295/20 , C07D263/38 , C07D307/68
CPC classification number: C07D239/10 , A61K38/00 , C07C271/22 , C07C317/44 , C07C323/60 , C07C2601/06 , C07C2601/14 , C07D233/32 , C07D263/06 , C07D263/20 , C07D263/22 , C07D263/24 , C07D263/26 , C07D265/06 , C07D273/00 , C07D295/205 , C07D295/215 , C07D307/58 , C07D307/68 , C07D317/36 , C07D333/38 , C07D413/06 , C07K5/06026 , C07K5/06043 , C07K5/06078 , C07K5/101 , C07K5/1016 , C07K7/02
Abstract: A retroviral protease inhibiting compound of the formula:
or a pharmaceutically acceptable salt, prodrug or ester thereof.
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