Methods of treating or preventing autoimmune diseases with 2,4-pyrimidinediamine compounds

Patent metadata

Field	Value
Publication number	US-9751893-B2
Application number	US-48748609-A
Country	US
Kind code	B2
Filing date	Jun 18, 2009
Priority date	Jul 30, 2003
Publication date	Sep 5, 2017
Grant date	Sep 5, 2017

Abstract

The present invention provides methods of treating or preventing autoimmune diseases with 2,4-pyrimidinediamine compounds, as well as methods of treating, preventing or ameliorating symptoms associated with such diseases. Specific examples of autoimmune diseases that can be treated or prevented with the compounds include rheumatoid arthritis and/or its associated symptoms, systemic lups erythematosis and/or its associated symptoms and multiple sclerosis and/or its associated symptoms.

First claim

What is claimed is:

1. A 2,4 pyrimidinediamine compound of the structural formula

or in the form of a salt or N-oxide thereof, in which
R 4 is

Y is selected from the group consisting of S, SO and SO 2 ;
Z is selected from the group consisting of NH and NR 35 ;
R 2 is
a)

 in which each R 31 is, independently of the others, methyl or (C1-C6) alkyl,
b)

 in which each R 31 is, independently of the others, methyl or (C1-C6) alkyl and yy is 1-6, or
c)

R 5 is selected from the group consisting of R 6 , (C1-C6) alkyl optionally substituted with one or more of the same or different R 8 groups, (C1-C4) alkanyl optionally substituted with one or more of the same or different R 8 groups, (C2-C4) alkenyl optionally substituted with one or more of the same or different R 8 groups and (C2-C4) alkynyl optionally substituted with one or more of the same or different R 8 groups;
each R 6 independently is selected from the group consisting of hydrogen, —OR d , —SR d , (C1-C3) haloalkyloxy, (C1-C3) perhaloalkyloxy, —NR c R c , halogen, (C1-C3) haloalkyl, (C1-C3) perhaloalkyl, —CF 3 , —CH 2 CF 3 , —CF 2 CF 3 , —CN, —NC, —OCN, —SCN, —NO, —NO 2 , —N 3 , —S(O)R d , —S(O) 2 R d , —S(O) 2 OR d , —S(O)NR c R c ; —S(O) 2 NR c R c , —OS(O)R d , —OS(O) 2 R d , —OS(O) 2 OR d , —OS(O)NR c R c , —OS(O) 2 NR c R c , —C(O)R d , —C(O)OR d , —C(O)NR c R c , —C(NH)NR c R c , —OC(O)R d , —SC(O)R d , —OC(O)OR d , —SC(O)OR d , —OC(O)NR c R c , —SC(O)NR c R c , —OC(NH)NR c R c , —SC(NH)NR c R c , —[NHC(O)] n R d , —[NHC(O)] n OR d , —[NHC(O)] n NR c R c and —[NHC(NH)] n NR c R c , (C5-C10) aryl optionally substituted with one or more of the same or different R 8 groups, phenyl optionally substituted with one or more of the same or different R 8 groups, (C6-C16) arylalkyl optionally substituted with one or more of the same or different R 8 groups, 5-10 membered heteroaryl optionally substituted with one or more of the same or different R 8 groups and 6-16 membered heteroarylalkyl optionally substituted with one or more of the same or different R 8 groups;
R 8 is selected from the group consisting of R a , R b , R a substituted with one or more of the same or different R a or R b , —OR a substituted with one or more of the same or different R a or R b , —B(OR a ) 2 , —B(NR c R c ) 2 , —(CH 2 ) m —R b , —(CHR a ) m —R b , —O—(CH 2 ) m —R b , —S—(CH 2 ) m —R b , —O—CHR a R b , —O—CR a (R b ) 2 , —O—(CHR a ) m —R b , —O—(CH 2 ) m —CH[(CH 2 ) m R b ]R b , —S—(CHR a ) m —R b , —C(O)NH—(CH 2 ) m —R b , —C(O)NH—(CHR a ) m —R b , —O—(CH 2 ) m —C(O)NH—(CH 2 ) m —R b , —S—(CH 2 ) m —C(O)NH—(CH 2 ) m —R b , —O—(CHR a ) m —C(O)NH—(CHR a ) m —R b , —S—(CHR a ) m —C(O)NH—(CHR a ) m —R b , —NH—(CH 2 ) m —R b , —NH—(CHR a ) m —R b , —NH[(CH 2 ) m R b ], —N[(CH 2 ) m R b ] 2 , —NH—C(O)—NH—(CH 2 ) m —R b , —NH—C(O)—(CH 2 ) m —CHR b R b and —NH—(CH 2 ) m —C(O)—NH—(CH 2 ) m —R b ;
each R 35 is, independently of the others, selected from the group consisting of hydrogen and R 8 , or, alternatively, two R 35 bonded to the same carbon atom are taken together to form an oxo (═O), NH or NR 38 group and the other two R 35 are each, independently of one another, selected from the group consisting of hydrogen and R 8 ;
R 38 is selected from the group consisting of (C1-C6) alkyl and (C5-C14) aryl;
each R a is independently selected from the group consisting of hydrogen, (C1-C6) alkyl, (C3-C8) cycloalkyl, cyclohexyl, (C4-C11) cycloalkylalkyl, (C5-C10) aryl, phenyl, (C6-C16) arylalkyl, benzyl, 2-6 membered heteroalkyl, 3-8 membered cycloheteroalkyl, morpholinyl, piperazinyl, homopiperazinyl, piperidinyl, 4-11 membered cycloheteroalkylalkyl, 5-10 membered heteroaryl and 6-16 membered heteroarylalkyl;
each R b is a suitable group independently selected from the group consisting of ═O, —OR d , (C1-C3) haloalkyloxy, —OCF 3 , ═S, —SR d , ═NR d , ═NOR d , —NR c R c , halogen, —CF 3 , —CN, —NC, —OCN, —SCN, —NO, —NO 2 , ═N 2 , —N 3 , —S(O)R d , —S(O) 2 R d , —S(O) 2 OR d , —S(O)NR c R c , —S(O) 2 NR c R c , —OS(O)R d , —OS(O) 2 R d , —OS(O) 2 OR d , —OS(O) 2 NR c R c , —C(O)R d , —C(O)OR d , —C(O)NR c R c , —C(NH)NR c R c , —C(NR a )NR c R c , —C(NOH)R a , —C(NOH)NR c R c , —OC(O)R d , —OC(O)OR d , —OC(O)NR c R c , —OC(NH)NR c R c , —OC(NR a )NR c R c , —[NHC(O)] n R d , —[NR a C(O)] n R d , —[NHC(O)] n OR d , —[NR a C(O)] n OR d , —[NHC(O)] n NR c R c , —[NR a C(O)] n NR c R c , —[NHC(NH)] n NR c R c and —[NR a C(NR a )] n NR c R c ;
each R c is independently R a , or, alternatively, each R c is taken together with the nitrogen atom to which it is bonded to form a 5 to 8-membered cycloheteroalkyl or heteroaryl which may optionally include one or more of the same or different additional heteroatoms and which may optionally be substituted with one or more of the same or different R a or suitable R b groups;
each R d is independently R a ;
each m is independently an integer from 1 to 3; and
each n is independently an integer from 0 to 3.

2. A compound according to claim 1 , wherein R 4 is

in which each R 35 is H or CH 3 .

3. A compound according to claim 1 , wherein R 4 is

in which each R 35 is H or CH 3 .

4. A compound according to claim 1 , wherein R 4 is

5. A compound according to claim 1 , wherein R 2 is

in which each R 31 is, independently of the others, methyl or (C1-C6) alkyl.

6. A compound according to claim 1 , wherein R 2 is

in which each R 31 is, independently of the others, methyl or (C1-C6) alkyl, and yy is 1 to 6.

7. A compound according to claim 1 , wherein R 5 is fluoro.

8. A compound according to claim 1 , wherein R 6 is hydrogen.

9. A compound according to claim 1 , wherein R 5 is fluoro and R 6 is hydrogen.

10. A compound, or salt or N-oxide thereof, that is
5-fluoro-N2-[3-(N-methylamino)carbonylmethyleneoxyphenyl]-N4-(3-oxo-2H,4H-benzo[1,4]thiazin-6-yl)-2,4-pyrimidinediamine;
N2-(3,5-dimethoxyphenyl)-5-fluoro-N4-(3-oxo-2H,4H-benzo[1,4]thiazin-6-yl)-2,4-pyrimidinediamine;
N2-(3-chloro-4-methoxyphenyl)-5-fluoro-N4-(3-oxo-2H,4H-benzo[1,4]thiazin-6-yl)-2,4-pyrimidinediamine;
N2-(3-chloro-4-methoxyphenyl)-5-fluoro-N4-(3-oxo-2H,4H-benzo[1,4]thiazin-6-yl)-2,4-pyrimidinediamine;
N2-(3-chloro-4-methoxyphenyl)-5-fluoro-N4-(3-oxo-2H,4H-benzo[1,4]thiazin-6-yl)-2,4-pyrimidinediamine;
N4-(3,4-dihydro-2H,4H-benzo[1,4]thiazin-6-yl)-5-fluoro-N2-[3-(N-methylamino)carbonylmethyleneoxyphenyl]-2,4-pyrim

Assignees

• Singh Rajinder
• Argade Ankush
• Li Hui
• Bhamidipati Somasekhar
• Carroll David
• Sylvain Catherine
• Clough Jeffrey
• Keim Holger
• Rigel Pharmaceuticals Inc

Inventors

• Singh Rajinder
• Argade Ankush
• Li Hui
• Bhamidipati Somasekhar
• Carroll David
• Sylvain Catherine
• Clough Jeffrey
• Keim Holger

Classifications

• A61K31/506

  not condensed and containing further heterocyclic rings · CPC title

• A61K31/541

  Non-condensed thiazines containing further heterocyclic rings · CPC title

• C07D417/12

  linked by a chain containing hetero atoms as chain links · CPC title

• C07D413/12

  linked by a chain containing hetero atoms as chain links · CPC title

• C07D403/12

  linked by a chain containing hetero atoms as chain links · CPC title