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1. 发明申请

US20210347813A1 COMPOUNDS WITH HIV MATURATION INHIBITORY ACTIVITY 有权
公开(公告)号：US20210347813A1
公开(公告)日：2021-11-11
申请号：US17046020
申请日：2019-04-22
申请人： VIIV HEALTHCARE UK (NO. 5) LIMITED
发明人： John F. KADOW , B. Narasimhulu NAIDU
IPC分类号： C07J63/00 , A61K31/58 , A61P31/18 , A61K31/5365 , A61K31/4985
摘要： The present invention relates to compound of Formula I or a pharmaceutically acceptable salt thereof wherein R1 is where the squiggly line indicates the point of attachment to the rest of the molecule; R2 is F or where the squiggly line indicates the point of attachment to the rest of the molecule; R3 is H or CH3; Z is O or is absent; and R4 is —OC1-3alkyl, C1-30alkyl, or —N(CH3)2.

2. 发明申请

US20190127351A1 PYRIDIN-3-YL ACETIC ACID DERIVATIVES AS INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION 审中-公开
公开(公告)号：US20190127351A1
公开(公告)日：2019-05-02
申请号：US16094536
申请日：2017-05-09
申请人： VIIV HEALTHCARE UK (NO 5) LIMITED
发明人： John F. KADOW , B. Narasimhulu NAIDU , Manoj PATEL , Michael A. WALKER , Tao WANG , Zhiwei YIN , Zhongxing ZHANG , Zhizhen Barbara ZHENG
IPC分类号： C07D401/14 , C07D401/04 , C07D405/14 , A61K31/5365 , A61K31/4725 , A61K31/4709 , A61K31/4545 , C07D409/14 , C07D413/14 , C07D411/14 , A61P31/18
CPC分类号： C07D401/14 , A61K31/4545 , A61K31/4709 , A61K31/4725 , A61K31/5365 , A61P31/18 , C07D401/04 , C07D405/14 , C07D407/14 , C07D409/14 , C07D411/14 , C07D413/14 , C07D417/14
摘要： Disclosed are compounds of Formula I, including pharmaceutically acceptable salts, pharmaceutical compositions comprising the compounds, methods for making the compounds and their use in inhibiting HIV integrase and treating those infected with HIV or AIDS.

3. 发明申请

US20180170904A1 PYRIDIN-3-YL ACETIC ACID DERIVATIVES AS INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION 审中-公开
公开(公告)号：US20180170904A1
公开(公告)日：2018-06-21
申请号：US15579993
申请日：2016-07-07
申请人： ViiV HEALTHCARE UK (NO.5) LIMITED
发明人： John F. KADOW , B. Narasimhulu NAIDU , Manoj PATEL , Jeffrey Lee ROMINE , Denis R. ST. LAURENT , Tao WANG , Zhongxing ZHANG
IPC分类号： C07D401/04 , C07D417/14 , C07D413/14 , A61P31/18
CPC分类号： C07D401/04 , A61P31/18 , C07D401/14 , C07D413/14 , C07D417/04 , C07D417/14
摘要： Disclosed are compounds of Formula I, including pharmaceutically acceptable salts, pharmaceutical compositions comprising the compounds, methods for making the compounds and their use in inhibiting HIV integrase and treating those infected with HIV or AIDS.

4. 发明公开

US20230192758A1 COMPOUNDS WITH HIV MATURATION INHIBITORY ACTIVITY 审中-公开
公开(公告)号：US20230192758A1
公开(公告)日：2023-06-22
申请号：US18096272
申请日：2023-01-12
申请人： VIIV HEALTHCARE UK (NO.5)LIMITED
发明人： John F. KADOW , B. Narasimhulu Naidu
IPC分类号： C07J63/00 , A61P31/18 , A61K31/4985 , A61K31/5365 , A61K31/58
CPC分类号： C07J63/008 , A61P31/18 , A61K31/4985 , A61K31/5365 , A61K31/58
摘要： The present invention relates to compound of Formula I or a pharmaceutically acceptable salt thereof

wherein R1 is

where the squiggly line indicates the point of attachment to the rest of the molecule;

R2 is F or

where the squiggly line indicates the point of attachment to the rest of the molecule;

R3 is H or CH3;

Z is O or is absent; and

R4 is —OC1-3alkyl, C1-30alkyl, or —N(CH3)2.

5. 发明申请

US20200325127A1 PYRIDIN-3-YL ACETIC ACID DERIVATIVES AS INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION 审中-公开
公开(公告)号：US20200325127A1
公开(公告)日：2020-10-15
申请号：US16094567
申请日：2017-05-09
申请人： ViiV HEALTHCARE UK (NO.5) LIMITED
发明人： John F. KADOW , B Narasimhulu NAIDU , Tao WANG , Zhiwei YIN , Zhongxing ZHANG
IPC分类号： C07D413/14 , C07D401/14 , C07D417/14 , C07D513/04 , C07D471/04
摘要： Disclosed are compounds of Formula I, including pharmaceutically acceptable salts, pharmaceutical compositions comprising the compounds, methods for making the compounds and their use in inhibiting HIV integrase and treating those infected with HIV or AIDS.

6. 发明申请

US20180162831A1 PYRIDIN-3-YL ACETIC ACID DERIVATIVES AS INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION 审中-公开
公开(公告)号：US20180162831A1
公开(公告)日：2018-06-14
申请号：US15579977
申请日：2016-07-06
申请人： VIIV HEALTHCARE UK (NO.5) LIMITED
发明人： John F. KADOW , B. Narasimhulu NAIDU , Manoj PATEL , Prasanna SIVAPRAKASAM
IPC分类号： C07D401/04 , C07D401/14 , C07D405/14 , C07D413/14 , C07D417/14 , A61P31/18
CPC分类号： C07D401/04 , A61P31/18 , C07D401/14 , C07D405/14 , C07D413/14 , C07D417/14
摘要： Disclosed are compounds of Formula I, including pharmaceutically acceptable salts, pharmaceutical compositions comprising the compounds, methods for making the compounds and their use in inhibiting HIV integrase and treating those infected with HIV or AIDS.

7. 发明申请

US20180230129A1 5-(N-BENZYL TETRAHYDROISOQUINOLIN-6-YL) PYRIDIN-3-YL ACETIC ACID DERIVATIVES AS INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION 审中-公开
公开(公告)号：US20180230129A1
公开(公告)日：2018-08-16
申请号：US15749176
申请日：2016-08-10
申请人： ViiV Healthcare UK (No.5) Limited
发明人： Kyle J. EASTMAN , John F. KADOW , Kyle E. PARCELLA , B. Narasimhulu NAIDU , Tao WANG , Zhiwei YIN , Zhongxing ZHANG
IPC分类号： C07D401/14 , A61P31/18
CPC分类号： C07D401/14 , A61K31/444 , A61K31/5365 , A61K2300/00 , A61P31/18 , C07D401/04
摘要： Disclosed are compounds of Formula (I), including pharmaceutically acceptable salts, pharmaceutical compositions comprising the compounds, methods for making the compounds and their use in inhibiting HIV integrase and treating those infected with HIV or AIDS. In the compounds of formula (I), R1 is selected from hydrogen, alkyl, or cycloalkyl; R2 is selected from tetrahydroisoquinolinyl and is substituted with 1 R6 substituent and also with 0-3 halo or alkyl substituents; R3 is selected from azetidinyl, pyrrolidinyl, piperidinyl, piperazinyl, morpholinyl, homopiperidinyl, homopiperazinyl, or homomorpholinyl, and is substituted with 0-3 substituents selected from cyano, halo, alkyl, haloalkyl, alkoxy, and haloalkoxy; R4 is selected from alkyl or haloalkyl; R5 is alkyl; R6 is selected from Ar1, (Ar1)alkyl, (chromanyl)alkyl, cyanocycloalkyl or (dihydrobenzodioxinyl)alkyl; and Ar1 is phenyl substituted with 0-5 substituents selected from cyano, halo, alkyl, cycloalkyl, haloalkyl, hydroxy, alkoxy, haloalkoxy, (hydroxy)alkoxy, (alkoxy)alkoxy, phenoxy, benzyloxy, carboxy, phenyl, and cyanocycloalkyl.

8. 发明申请

US20210024503A1 4-OXO-3,4-DIHYDROQUINAZOLINE COMPOUNDS AS INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION 有权
公开(公告)号：US20210024503A1
公开(公告)日：2021-01-28
申请号：US17042413
申请日：2019-04-11
申请人： VIIV HEALTHCARE UK (NO. 5) LIMITED
发明人： Makonen BELEMA , John A. BENDER , David B. FRENNESSON , Eric P. GILLIS , Christiana IWUAGWU , John F. KADOW , B. Narasimhulu NAIDU , Kyle E. PARCELLA , Kevin M. PEESE , Ramkumar RAJAMANI , Mark G. SAULNIER , Alan Xiangdong WANG , Manoj PATEL , Michael S. BOWSHER
IPC分类号： C07D403/14 , A61P31/18 , C07D403/12 , C07D401/14 , C07D405/14 , C07D413/14 , C07D491/052
摘要： Compounds of Formula I, including pharmaceutically acceptable salts thereof, and compositions and methods for treating human immunodeficiency virus (HIV) infection are set forth:

9. 发明申请

US20190152957A1 PYRIDIN-3-YL ACETIC ACID DERIVATIVES AS INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION 审中-公开
公开(公告)号：US20190152957A1
公开(公告)日：2019-05-23
申请号：US16096716
申请日：2017-05-09
申请人： ViiV HEALTHCARE UK (NO.5) LIMITED
发明人： John F. KADOW , B. Narasimhulu NAIDU , Tao WANG , Zhongxing ZHANG
IPC分类号： C07D405/14 , C07D401/14 , C07D417/14 , C07D413/14 , A61P31/18 , A61K31/5365 , A61K31/4725 , A61K31/506 , A61K31/501
摘要： Disclosed are compounds of Formula I, including pharmaceutically acceptable salts, pharmaceutical compositions comprising the compounds, methods for making the compounds and their use in inhibiting HIV integrase and treating those infected with HIV or AIDS.

10. 发明申请

US20190010139A1 PYRIDIN-3-YL ACETIC ACID DERIVATIVES AS INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION 审中-公开
公开(公告)号：US20190010139A1
公开(公告)日：2019-01-10
申请号：US15748791
申请日：2016-08-03
申请人： ViiV Healthcare UK (No.5) Limited
发明人： John F. KADOW , B. Narasimhulu NAIDU , Jeffrey Lee ROMINE , Denis R. ST. LAURENT , Prasanna SIVAPRAKASAM
IPC分类号： C07D401/04 , A61P31/18 , C07D401/14 , C07D407/14 , C07D471/10 , C07D493/10
摘要： Disclosed are compounds of Formula I, including pharmaceutically acceptable salts, pharmaceutical compositions comprising the compounds, methods for making the compounds and their use in inhibiting HIV integrase and treating those infected with HIV or AIDS. In the compounds of formula I, R1 is selected from H, alkyl, haloalkyl, hydroxyalkyl, alkoxyalkyl, (alkoxy)alkoxyalkyl, or (R6)alkyl; R2 is phenyl substituted with 1 R7 substituent and with 0-3 substituents selected from halo, alkyl, haloalkyl, alkoxy, and haloalkoxy; or R2 is selected from tetrahydroisoquinolinyl, ((Ar1)alkyl)tetrahydroisoquinolinyl, or ((N-alkoxycarbonyl) tetrahydroisoquinolinyl; R3 is selected from tetrahydroisoquinolinyl or decahydroisoquinolinyl and is substituted with 0-3 substituents selected from halo, alkyl, and haloalkyl; or R3 is a [5-7.3-7.0-2] fused or bridged bicyclic amine and is substituted with 0-3 alkyl substituents; or R3 is selected from azetidinyl, pyrrolidinyl, piperidinyl, or homopiperidinyl and contains a spirocyclic moiety wherein the spirocyclic moiety, including the carbon atom to which it is attached, forms C3-7 cycloalkane, tetrahydrofuranyl, tetrahydropyranyl, pyrrolidinyl, N-alkylpyrrolidinyl, piperidinyl, N-alkylpiperidinyl, homopiperidinyl, or N-alkylpiperidinyl, and wherein the spirocyclic moiety is substituted with 0-3 halo or alkyl substituents; R4 is selected from alkyl or haloalkyl; R5 is selected from H, alkyl, haloalkyl, hydroxyalkyl, alkoxyalkyl, (alkoxy)alkoxyalkyl, or (R6) alkyl; R6 is selected from (oxetanyl)oxy, ((oxetanyl)alkoxy)alkyl, (tetrahydropyranyloxy)alkyl, (tetrahydropyranyl)alkoxy)alkyl, or (R9)(R9)N; R7 is selected from (Ar1)alkoxy or ((Ar1)alkyl)HNCO; R8 is selected from hydrogen, alkyl, (cycloalkyl)alkyl, alkoxyalkyl, (tetrahydropyanyl)alkyl, tetrahydropyanyl, or alkoxyphenyl; R9 is selected from hydrogen or alkyl; or (R8)(R9)N taken together is selected from azetidinyl, pyrrolidinyl, piperidinyl, (spirocyclobutyl) piperidinyl, piperazinyl, or morpholinyl; and Ar1 is phenyl substituted with 0-3 substituents selected from halo, alkyl, haloalkyl, alkoxy, and haloalkoxy.

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