公开(公告)号：MX9204259A

公开(公告)日：1993-02-01

申请号：MX9204259

申请日：1992-07-21

Applicant: ABBOTT LAB

Inventor： KEMPF DALE J ,  NORBECK DANIEL W ,  CODACOVI LYNN M ,  PLATTNER JACOB J ,  SHAM HING LEUNG ,  CHENZHAO ,  WITTENBERGER STEVEN J

IPC: C12N15/00

公开(公告)号：CA2393271A1

公开(公告)日：1992-05-21

申请号：CA2393271

申请日：1991-11-15

Applicant: ABBOTT LAB

Inventor： WITTENBERGER STEVEN J ,  ZHAO CHEN ,  SHAM HING L ,  PLATTNER JACOB J ,  KEMPF DALE J ,  CODACOVI LYNN M ,  NORBECK DANIEL W

IPC: A61K31/42 ,  A61K31/421 ,  A61K31/425 ,  A61K31/426 ,  A61K31/427 ,  A61K31/435 ,  A61K31/4402 ,  A61K31/4406 ,  A61K31/4409 ,  A61K31/4418 ,  A61K31/4427 ,  A61K31/443 ,  A61K31/444 ,  A61K38/00 ,  A61P31/12 ,  A61P31/18 ,  A61P43/00 ,  C07C53/134 ,  C07C211/00 ,  C07C215/18 ,  C07C215/20 ,  C07C215/28 ,  C07C215/30 ,  C07C215/80 ,  C07C219/18 ,  C07C233/40 ,  C07C237/10 ,  C07C237/22 ,  C07C269/04 ,  C07C271/02 ,  C07C271/16 ,  C07C271/20 ,  C07C271/22 ,  C07C271/34 ,  C07C275/24 ,  C07D20060101 ,  C07D213/00 ,  C07D213/26 ,  C07D213/30 ,  C07D213/34 ,  C07D213/36 ,  C07D213/40 ,  C07D213/54 ,  C07D213/56 ,  C07D213/61 ,  C07D213/75 ,  C07D213/79 ,  C07D215/20 ,  C07D233/54 ,  C07D233/84 ,  C07D235/14 ,  C07D235/16 ,  C07D237/10 ,  C07D239/26 ,  C07D241/12 ,  C07D261/08 ,  C07D261/12 ,  C07D263/20 ,  C07D263/32 ,  C07D277/20 ,  C07D277/24 ,  C07D277/28 ,  C07D277/30 ,  C07D277/32 ,  C07D277/34 ,  C07D277/36 ,  C07D277/40 ,  C07D277/42 ,  C07D277/56 ,  C07D295/02 ,  C07D295/13 ,  C07D295/205 ,  C07D295/215 ,  C07D303/36 ,  C07D307/34 ,  C07D307/42 ,  C07D307/66 ,  C07D333/16 ,  C07D333/36 ,  C07D401/12 ,  C07D405/12 ,  C07D413/12 ,  C07D417/12 ,  C07D471/04 ,  C07D521/00 ,  C07K1/113 ,  C07K5/06 ,  C07K5/065 ,  C07K5/08 ,  C07K14/81

Abstract: A retroviral protease inhibiting compound is diclosed. The compound is of the formula (see formule I) wherein R1 is hydrogen and R2 and R3 are independently selected from C6-aryl-C1-to-C6-alkyl, C9-to-C10-aryl-C1-to-C6-alkyl, C3-to-C7- cycloalkyl-C1-to-C6-alkyl and (heterocyclic)-C1-to-C6-alkyl; and A and B are independently selected from R6-C(O)-(NH)-(CH(R5))- C(O)- and R6-C(O)- wherein at each occurrence R6 is independently selected from R7-N(C1-to-C6-loweralkyl)-, R7-O- and R7-S- wherein R7 is heterocyclic or (heterocyclic)-C1-to-C6-alkyl and at each occurrence R5 is independently selected from C1-to-C6-loweralkyl; or a pharmaceutically acceptable salt, thereof. Also disclosed are a composition use and kit 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.

公开(公告)号：SG188878A1

公开(公告)日：2013-04-30

申请号：SG2013017603

申请日：2007-02-16

Applicant: ABBOTT LAB

Inventor： COWART MARLON D ,  ZHAO CHEN ,  SUN MINGHUA ,  BLACK LAWRENCE A ,  ZHENG GUO ZHU ,  GREGG ROBERT J ,  ZHANG GEOFF G Z ,  SHEIKH AHMAD Y ,  LOU XIAOCHUN ,  HENRY RODGER F ,  BARNES DAVID M ,  KOLACZKOWSKI LAWRENCE ,  HAIGHT ANTHONY R ,  CHANG SOU-JEN ,  WITTENBERGER STEVEN J ,  FICKES MICHAEL G

Abstract: Octahydro-pyrrolo[3,4-b]pyrrole derivatives are useful in treating conditions or disorders prevented by or ameliorated by histamine-3 receptor ligands. Octahydro-pyrrolo[3,4-b]pyrrole compounds, methods for using such compounds, compositions for making them, and processes for preparing such compounds are disclosed herein.Figure 1

公开(公告)号：SG170033A1

公开(公告)日：2011-04-29

申请号：SG2011013430

申请日：2007-02-16

Applicant: ABBOTT LAB

Inventor： COWART MARLON D ,  ZHAO CHEN ,  SUN MINGHUA ,  BLACK LAWRENCE A ,  ZHENG GUO ZHU ,  GREGG ROBERT J ,  ZHANG GEOFF G Z ,  SHEIKH AHMAD Y ,  LOU XIAOCHUN ,  HENRY RODGER F ,  BARNES DAVID M ,  KOLACZKOWSKI LAWRENCE ,  HAIGHT ANTHONY R ,  CHANG SOU-JEN ,  WITTENBERGER STEVEN J ,  FICKES MICHAEL G

Abstract: OCTAHYDRO-PYRROLO[3,4-B] PYRROLE DERIVATIVES AND THEIR USE AS HISTAMINE-3 RECEPTOR LIGANDS Octahydro-pyrrolo[3,4-b]pyrrole derivatives are useful in treating conditions or disorders prevented by or ameliorated by histamine-3 receptor ligands. Octahydro-pyrrolo[3,4-b]pyrrole compounds, methods for using such compounds, compositions for making them, and processes for preparing such compounds are disclosed herein.

公开(公告)号：NZ552520A

公开(公告)日：2010-09-30

申请号：NZ55252005

申请日：2005-07-08

Applicant: ABBOTT LAB

Inventor： BUCKLEY MICHAEL J ,  JL JIANGUO ,  ZHANG GEOFF G ,  HENRY RODGER F ,  WANG WEILI W ,  WAYNE GREG S ,  LL WENKE ,  TOWNE TIMOTHY B ,  WITTENBERGER STEVEN J ,  HANNICK STEVEN M ,  KOTECKI BRIAN J ,  MARCI BRYAN S ,  ROBBINS TIMOTHY A

IPC: A61K31/4439 ,  C07D487/04

Abstract: Disclosed is a salt of (1S,5S)-3-(5,6-dichloro-3-pyridinyl)-3,6-diazabicyclo[3.2.0]heptane, selected from the group consisting of acetate, citrate, fumarate, hemicitrate, hydrocholoride, maleate, methanesulfonate, 4-methylbenzenesulfonate, sulphate, L-tartrate and trifluoroacetate. Also disclosed is a process for preparing a compound of formula (5J) comprising the steps of a) treating compound (5D), with an aqueous acid; b) treating the mixture from step (a) with a compound of formula (A), wherein R2 is phenyl optionally substituted with alkyl, alkoxy or halo in the presence of magnesium bromide in a mixture of isopropyl alcohol and dichloromethane to provide a compound of formula (B), c) using the compound of formula (B) to prepare the compound (5J).

公开(公告)号：ECSP088687A

公开(公告)日：2008-09-29

申请号：ECSP088687

申请日：2008-08-20

Applicant: ABBOTT LAB

Inventor： SHEIKH AHMAD YAHYA ,  ZHAO CHEN ,  HAIGHT ANTHONY R ,  COWART MARLON D ,  SUN MINGHUA ,  ZHENG GUO ZHU ,  HENRY RODGER F ,  WITTENBERGER STEVEN J ,  BARNES DAVID ,  BLACK LAWRENCE A ,  GREGG ROBERT J ,  ZHANG GEOFF G Z ,  LOU XIAOCHUN ,  KOLACZKOWSKI LAWRENCE ,  CHANG SOU-JEN ,  FICKES MICHAEL G

IPC: A61K31/407

Abstract: Derivados de octahidro-pirrolo[3,4-b]pirrol útiles para tratar condiciones o trastornos que se previenen o mejoran con ligandos del receptor de histamina-3. En la presente se divulgan compuestos octahidro-pirrolo[3,4-b]pirrol, métodos para usar dichos compuestos, composiciones para hacerlos, y procesos para preparar dichos compuestos.

公开(公告)号：AU2008201198A1

公开(公告)日：2008-04-03

申请号：AU2008201198

申请日：2008-03-12

Applicant: ABBOTT LAB

Inventor： SZCZEPANKIEWICZ BRUCE G ,  WITTENBERGER STEVEN J ,  JAE HWAN-SOO ,  BOYD STEVEN A ,  KESTER JEFFREY A ,  KING STEVEN A ,  WINN MARTIN ,  HENRY KENNETH J ,  LIU GANG ,  TASKER ANDREW S ,  HUTCHINS CHARLES W ,  SORENSEN BRYAN K ,  GELDEM THOMAS W VON

IPC: C07D405/00

公开(公告)号：CA2393271C

公开(公告)日：2007-12-11

申请号：CA2393271

申请日：1991-11-15

Applicant: ABBOTT LAB

Inventor： KEMPF DALE J ,  NORBECK DANIEL W ,  WITTENBERGER STEVEN J ,  CODACOVI LYNN M ,  SHAM HING L ,  PLATTNER JACOB J ,  ZHAO CHEN

IPC: A61K31/42 ,  C07D277/28 ,  A61K31/421 ,  A61K31/425 ,  A61K31/426 ,  A61K31/427 ,  A61K31/435 ,  A61K31/4402 ,  A61K31/4406 ,  A61K31/4409 ,  A61K31/4418 ,  A61K31/4427 ,  A61K31/443 ,  A61K31/444 ,  A61K38/00 ,  A61P31/12 ,  A61P31/18 ,  A61P43/00 ,  C07C53/134 ,  C07C211/00 ,  C07C215/18 ,  C07C215/20 ,  C07C215/28 ,  C07C215/30 ,  C07C215/80 ,  C07C219/18 ,  C07C233/40 ,  C07C237/10 ,  C07C237/22 ,  C07C269/04 ,  C07C271/02 ,  C07C271/16 ,  C07C271/20 ,  C07C271/22 ,  C07C271/34 ,  C07C275/24 ,  C07D20060101 ,  C07D213/00 ,  C07D213/26 ,  C07D213/30 ,  C07D213/34 ,  C07D213/36 ,  C07D213/40 ,  C07D213/54 ,  C07D213/56 ,  C07D213/61 ,  C07D213/75 ,  C07D213/79 ,  C07D215/20 ,  C07D233/54 ,  C07D233/84 ,  C07D235/14 ,  C07D235/16 ,  C07D237/10 ,  C07D239/26 ,  C07D241/12 ,  C07D261/08 ,  C07D261/12 ,  C07D263/20 ,  C07D263/32 ,  C07D277/20 ,  C07D277/24 ,  C07D277/30 ,  C07D277/32 ,  C07D277/34 ,  C07D277/36 ,  C07D277/40 ,  C07D277/42 ,  C07D277/56 ,  C07D295/02 ,  C07D295/13 ,  C07D295/205 ,  C07D295/215 ,  C07D303/36 ,  C07D307/34 ,  C07D307/42 ,  C07D307/66 ,  C07D333/16 ,  C07D333/36 ,  C07D401/12 ,  C07D405/12 ,  C07D413/12 ,  C07D417/12 ,  C07D471/04 ,  C07D521/00 ,  C07K1/113 ,  C07K5/06 ,  C07K5/065 ,  C07K5/08 ,  C07K14/81

Abstract: A retroviral protease inhibiting compound is diclosed. The compound is of the formula (see formula I) wherein R1 is hydrogen and R2 and R3 are independently selected from C6-aryl-C1-to-C6-alkyl, C9-to-C10-aryl-C1-to-C6-alkyl, C3-to-C7- cycloalkyl-C1-to-C6-alkyl and (heterocyclic)-C1-to-C6-alkyl; and A and B are independently selected from R6-C(O)-(NH)-(CH(R5))- C(O)- and R6-C(O)- wherein at each occurrence R6 is independently selected from R7-N(C1-to-C6-loweralkyl)-, R7-O- and R7-S- wherein R7 is heterocyclic or (heterocyclic)-C1-to-C6-alkyl and at each occurrence R5 is independently selected from C1-to-C6-loweralkyl; or a pharmaceutically acceptable salt, thereof. Also disclosed are a composition use and kit 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.

公开(公告)号：DK0885215T3

公开(公告)日：2006-08-14

申请号：DK97905816

申请日：1997-02-12

Applicant: ABBOTT LAB

Inventor： WINN MARTIN ,  VON GELDERN THOMAS W ,  SORENSEN BRYAN K ,  LIU GANG ,  BOYD STEVEN A ,  HUTCHINS CHARLES W ,  JAE HWAN-SOO ,  TASKER ANDREW S ,  KESTER JEFFREY A ,  SZCZEPANKIEWICZ BRUCE G ,  HENRY KENNETH J JR ,  WITTENBERGER STEVEN J ,  KING STEVEN A

IPC: C07D405/04 ,  A61K31/395 ,  A61K31/40 ,  A61K31/4015 ,  A61K31/4035 ,  A61K31/41 ,  A61K31/415 ,  A61K31/4164 ,  A61K31/4166 ,  A61K31/421 ,  A61K31/425 ,  A61K31/435 ,  A61K31/4439 ,  A61K31/454 ,  A61K31/495 ,  A61K31/506 ,  A61K31/675 ,  A61P1/00 ,  A61P1/04 ,  A61P7/02 ,  A61P9/00 ,  A61P9/04 ,  A61P9/10 ,  A61P9/12 ,  A61P11/00 ,  A61P11/06 ,  A61P13/12 ,  A61P25/06 ,  A61P43/00 ,  C07D207/16 ,  C07D211/60 ,  C07D401/04 ,  C07D403/04 ,  C07D405/12 ,  C07D405/14 ,  C07D409/14 ,  C07D413/14 ,  C07D417/14 ,  C07D419/14 ,  C07D453/02 ,  C07D471/04 ,  C07D491/04 ,  C07F9/572 ,  C07F9/59

Abstract: A compound of formula (I), or a pharmaceutically acceptable salt thereof is disclosed, as well as processes for and intermediates in the preparation thereof, and a method of antagonizing endothelin.

公开(公告)号：AT294809T

公开(公告)日：2005-05-15

申请号：AT00942860

申请日：2000-06-15

Applicant: ABBOTT LAB

Inventor： STONER ERIC J ,  PETERSON MATTHEW J ,  KU YI-YIN ,  CINK RUSSELL D ,  COOPER ARTHUR J ,  DESHPANDE MAHENDRA N ,  GRIEME TIM ,  HAIGHT ANTHONY R ,  HILL DAVID R ,  HSU MARGARET CHI-PING ,  KING STEVEN A ,  LEANNA MARVIN R ,  LEE ELAINE C ,  MCLAUGHLIN MAUREEN A ,  MORTON HOWARD E ,  NAPIER JAMES J ,  PLATA DANIEL J ,  RAJE PRASAD S ,  RASMUSSEN MICHAEL ,  RILEY DAVID ,  TIEN JIEN-HEH J ,  WITTENBERGER STEVEN J

IPC: A61P31/04 ,  C07B61/00 ,  C07H1/00 ,  C07H17/08 ,  A61K31/70

Abstract: In one aspect, the invention relates to a process for preparing 6-O-substituted erythromycin derivatives comprising reacting 2'-substituted and optionally 4''-substituted 9-oxime erythromycin derivatives with an alkylating agent in the presence of a palladium catalyst and phosphine. In another aspect, the invention relates to processes for preparing 6-O-substituted erythromycin ketolides using the palladium-catalyzed alkylation reaction.