WO2010054398A1 - Compounds useful as inhibitors of atr kinase - Google Patents

Compounds useful as inhibitors of atr kinase Download PDF

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Publication number
WO2010054398A1
WO2010054398A1 PCT/US2009/063922 US2009063922W WO2010054398A1 WO 2010054398 A1 WO2010054398 A1 WO 2010054398A1 US 2009063922 W US2009063922 W US 2009063922W WO 2010054398 A1 WO2010054398 A1 WO 2010054398A1
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WO
WIPO (PCT)
Prior art keywords
compound
aliphatic
alkyl
optionally substituted
ring
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/US2009/063922
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English (en)
French (fr)
Inventor
Jean-Damien Charrier
Steven Durrant
David Kay
Michael O'donnell
Ronald Knegtel
Somhairle Maccormick
Joanne Pinder
Anisa Virani
Stephen Young
Hayley Binch
Thomas Cleveland
Lev T.D. Fanning
Dennis Hurley
Pramod Joshi
Urvi Sheth
Alina Silina
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Vertex Pharmaceuticals Inc
Original Assignee
Vertex Pharmaceuticals Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to CN200980152891.XA priority Critical patent/CN102264721B/zh
Priority to KR1020177002740A priority patent/KR20170015566A/ko
Priority to CA2743134A priority patent/CA2743134A1/en
Priority to MX2011004953A priority patent/MX2011004953A/es
Priority to JP2011535772A priority patent/JP5702293B2/ja
Priority to AU2009313198A priority patent/AU2009313198B2/en
Priority to KR1020117013234A priority patent/KR101712576B1/ko
Priority to HK12102078.7A priority patent/HK1161260B/xx
Priority to RU2011123647/04A priority patent/RU2011123647A/ru
Application filed by Vertex Pharmaceuticals Inc filed Critical Vertex Pharmaceuticals Inc
Priority to EP09756203A priority patent/EP2370424A1/en
Priority to NZ593316A priority patent/NZ593316A/xx
Publication of WO2010054398A1 publication Critical patent/WO2010054398A1/en
Priority to ZA2011/03411A priority patent/ZA201103411B/en
Anticipated expiration legal-status Critical
Priority to IL212817A priority patent/IL212817A/en
Priority to US13/104,291 priority patent/US8410112B2/en
Priority to US13/742,948 priority patent/US20140113005A1/en
Ceased legal-status Critical Current

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    • C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
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    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4965—Non-condensed pyrazines
    • A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
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    • A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/541—Non-condensed thiazines containing further heterocyclic rings
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    • A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
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    • C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D241/24—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
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    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10—Spiro-condensed systems
    • C07D491/113—Spiro-condensed systems with two or more oxygen atoms as ring hetero atoms in the oxygen-containing ring

Definitions

  • R 1 is a 5-membered ring optionally fused to another ring.
  • R 1 is a monocyclic 5-membered ring containing 1-3 heteroatoms selected from oxygen, nitrogen, or sulfur.
  • R 1 is a 5-membered ring and is selected from the following:
  • R is H or Ci_ 4 alkyl wherein said Ci_ 4 alkyl is optionally substituted with 1-4 halo.
  • J is fluoro or a moiety containing a hydrogen bond acceptor
  • V 1 is Ci_6 aliphatic chain wherein up to three methylene unit of the aliphatic chain may be optionally replaced with -NR'-, -O-, -S-, -C(O)-, -S(O)-, or -S(O) 2 -; wherein the first or second methylene group away from the point of attachment is replaced with CO, SO, SO 2 , S, or O; R' is H or Ci_ 4 alkyl;
  • V is a Ci_ioaliphatic chain wherein 0-3 methylene units are optionally replaced with -NR-, -O-,
  • Q 2 is a 3-8 membered saturated or unsaturated monocyclic ring having 0-4 heteroatoms independently selected from nitrogen, oxygen, or sulfur, or a 8-10 membered saturated or unsaturated bicyclic ring having 0-6 heteroatoms independently selected from nitrogen, oxygen, or sulfur; each Q 2 is optionally substituted with 1-5 J Q2 ;
  • V is O, O(C 1-6 alkyl), (C 1-4 alkyl)O, C(O)O, C(O)O(Ci. ealkyl), C(O)O(Ci_ 6 alkyl)O(Ci_ 6 alkyl), C(O)(C i_ 6 alkyl), C(O)(Ci_ 6 alkyl)N, C(O)(Ci. 6 alkyl)NH(Ci. 6 alkyl), C(O)(Ci_ 6 alkyl)C(O)O, C(O)(Ci_ 6 alkyl)O, C(O)(Ci. 6 alkyl)O(Ci. 6 alkyl), C(O)(Ci. 6 alkyl)NH(Ci. 6 alkyl),
  • Q 2 is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, phenyl, imidazolyl, thienyl, thiazolyl, furanyl, pyrazolyl, triazolyl, tetrazolyl, pyrrolyl, phenyl, pyridyl, pyrimidyl, pyrazinyl, pyrrolidinyl, piperidinyl, piperazinyl, homopiperidinyl, homopiperazinyl, morpholinyl, thiomorpholinyl, or tetrahydropyranyl; wherein said Q 2 is optionally substituted with Ci_ 6 alkyl, CN, halo, haloCi_ 4 alkyl, NH(C M alkyl), N(Ci_ 4 alkyl) 2 , or O(C 1-6 alkyl).
  • J is selected from, oxo, -OH, -NHC(O)(C i_ 4 alkyl), -C(O)(Ci. 4 alkyl), -C(O)NH 2 , -C(O)NH(Ci_ 4 alkyl), -C(O)NH(C i_ 4 alkyl) 2 , -S(O) 2 (Ci_ 4 alkyl), -S(O) 2 NH(Ci. 4 alkyl), or -S(O) 2 N(Ci_ 4 alkyl) 2 .
  • cycloaliphatic refers to a monocyclic C3-C8 hydrocarbon or bicyclic Cs-Ci 2 hydrocarbon that is completely saturated or that contains one or more units of unsaturation, but which is not aromatic, that has a single point of attachment to the rest of the molecule wherein any individual ring in said bicyclic ring system has 3-7 members.
  • cycloaliphatic groups include, but are not limited to, cycloalkyl and cycloalkenyl groups. Specific examples include, but are not limited to, cyclohexyl, cyclopropenyl, and cyclobutyl.
  • the pharmaceutical compositions of this invention may be administered in the form of suppositories for rectal administration. These can be prepared by mixing the agent with a suitable non-irritating excipient that is solid at room temperature but liquid at rectal temperature and therefore will melt in the rectum to release the drug. Such materials include, but are not limited to, cocoa butter, beeswax and polyethylene glycols.
  • a suitable non-irritating excipient that is solid at room temperature but liquid at rectal temperature and therefore will melt in the rectum to release the drug.
  • Such materials include, but are not limited to, cocoa butter, beeswax and polyethylene glycols.
  • the pharmaceutical compositions of this invention may also be administered topically, especially when the target of treatment includes areas or organs readily accessible by topical application, including diseases of the eye, the skin, or the lower intestinal tract. Suitable topical formulations are readily prepared for each of these areas or organs.
  • Topical application for the lower intestinal tract can be effected in a rectal
  • additional drugs which are normally administered to treat or prevent that condition, may be administered together with the compounds of this invention.
  • an "effective amount" of the compound or pharmaceutically acceptable composition is that amount effective in order to treat said disease.
  • the compounds and compositions, according to the method of the present invention may be administered using any amount and any route of administration effective for treating or lessening the severity of said disease.
  • Pyrimidine family include Cytarabine, gemcitabine, 5-Fluorouracil (5FU) and relatives.
  • Some other specific examples of antimetabolites include Aminopterin, Methotrexate, Pemetrexed,
  • the bromine atom in iii.3 can then be used as a handle for nucleophilic displacement with a cyclic amine to generate compounds vi of this invention where R 2 is linked to the aminopyrazine moiety through a nitrogen atom.
  • the bromine atom in iii.3 can also be used as a handle for metal-catalyzed cross-coupling (e.g., palladium catalyzed coupling with a boronic acid) to generate compounds x of this invention where R 2 is linked to the aminopyrazine moiety through a carbon atom.
  • Step 3 4-(5-amino-6-(6-methyl-lH-benzo[d]imidazol-2-yl)pyrazin-2-yl)-N,N-dimethyl-5,6- dihydropyridine-l(2H)-sulfonamide (Compound 1-23)
  • Compound 1-16 was prepared using Method A, Steps 1-3 followed by Method P, Steps 1-3.
  • Compound 1-73 was also prepared using Method A, Step 1 followed by Method B, Steps 1-4 followed by Method S, Steps 1-2 followed by Method T, Step 1.
  • Compound 1-73 (E)-l-(3-amino-6-(4-(ethylsulfonyl)piperazin-l-yl)pyrazin-2-yl)-3-phenylprop- 2-en-l-one; IH NMR (400.0 MHz, DMSO) d 1.21 (t, 3H), 3.13 (q, 2H), 3.35-3.37 (m, 4H), 3.54- 3.57 (m, 4H), 7.47-7.51 (m, 3H), 7.55 (br s, 2H), 7.72 (d, IH), 7.79-7.81 (m, 2H), 8.28 (d, IH), 8.41 (s, IH) ppm; MS (ES + ) 402.01
  • Step 7 3-(l-(4-aminophenyl)-lH-l,2,3-triazol-4-yl)-5-(4- (ethylsulfonyl)piperazin-l-yl)pyrazin-2-amine

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CA2743134A CA2743134A1 (en) 2008-11-10 2009-11-10 Compounds useful as inhibitors of atr kinase
EP09756203A EP2370424A1 (en) 2008-11-10 2009-11-10 Compounds useful as inhibitors of atr kinase
JP2011535772A JP5702293B2 (ja) 2008-11-10 2009-11-10 Ａｔｒキナーゼの阻害剤として有用な化合物
AU2009313198A AU2009313198B2 (en) 2008-11-10 2009-11-10 Compounds useful as inhibitors of ATR kinase
KR1020117013234A KR101712576B1 (ko) 2008-11-10 2009-11-10 Ａｔｒ 키나제의 억제제로서 유용한 화합물
HK12102078.7A HK1161260B (en) 2008-11-10 2009-11-10 Compounds useful as inhibitors of atr kinase
CN200980152891.XA CN102264721B (zh) 2008-11-10 2009-11-10 用作atr激酶抑制剂的化合物
MX2011004953A MX2011004953A (es) 2008-11-10 2009-11-10 Compuestos utiles como inhibidores de cinasa atr.
KR1020177002740A KR20170015566A (ko) 2008-11-10 2009-11-10 Ａｔｒ 키나제의 억제제로서 유용한 화합물
NZ593316A NZ593316A (en) 2008-11-10 2009-11-10 Pyrazine compounds useful as inhibitors of atr kinase
ZA2011/03411A ZA201103411B (en) 2008-11-10 2011-05-10 Compounds useful as inhibitors of atr kinase
IL212817A IL212817A (en) 2008-11-10 2011-05-11 Atr kinase suppressants, preparations containing them and their uses
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