AU2017296289A1 - 2,5-disubstituted 3-methyl pyrazines and 2,5,6-trisubstituted 3-methyl pyrazines as allosteric SHP2 inhibitors - Google Patents
2,5-disubstituted 3-methyl pyrazines and 2,5,6-trisubstituted 3-methyl pyrazines as allosteric SHP2 inhibitors Download PDFInfo
- Publication number
- AU2017296289A1 AU2017296289A1 AU2017296289A AU2017296289A AU2017296289A1 AU 2017296289 A1 AU2017296289 A1 AU 2017296289A1 AU 2017296289 A AU2017296289 A AU 2017296289A AU 2017296289 A AU2017296289 A AU 2017296289A AU 2017296289 A1 AU2017296289 A1 AU 2017296289A1
- Authority
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- Australia
- Prior art keywords
- heterocycle
- heteroaryl
- optionally substituted
- independently
- c6alkyl
- 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.)
- Abandoned
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- 0 CC1=C(*)*C(C)=C(*N)*1 Chemical compound CC1=C(*)*C(C)=C(*N)*1 0.000 description 12
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- AXMNGEUJXLXFRY-UHFFFAOYSA-N C(CC1)CC11CCNCC1 Chemical compound C(CC1)CC11CCNCC1 AXMNGEUJXLXFRY-UHFFFAOYSA-N 0.000 description 1
- SLUGDMQHACBGSL-UHFFFAOYSA-N CC(C)(C)OC(NC(C)(CC1)CCN1c(cn1)nc(C)c1Br)=O Chemical compound CC(C)(C)OC(NC(C)(CC1)CCN1c(cn1)nc(C)c1Br)=O SLUGDMQHACBGSL-UHFFFAOYSA-N 0.000 description 1
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- DEUKTGSTJGOTFC-UHFFFAOYSA-N CC(C)(C)OC(NC(C)(CC1)CCN1c1nc(I)c(-c(cccc2Cl)c2Cl)nc1)=O Chemical compound CC(C)(C)OC(NC(C)(CC1)CCN1c1nc(I)c(-c(cccc2Cl)c2Cl)nc1)=O DEUKTGSTJGOTFC-UHFFFAOYSA-N 0.000 description 1
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- BWRYEIRJKXWIPJ-CYBMUJFWSA-N CCOC(c1c(N(CC2)CCC2(CCC2)[C@@H]2N)nc(C)cn1)=O Chemical compound CCOC(c1c(N(CC2)CCC2(CCC2)[C@@H]2N)nc(C)cn1)=O BWRYEIRJKXWIPJ-CYBMUJFWSA-N 0.000 description 1
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- LZCHEXJJOKRTHE-UHFFFAOYSA-N CCOC(c1ncc(C)nc1Cl)=O Chemical compound CCOC(c1ncc(C)nc1Cl)=O LZCHEXJJOKRTHE-UHFFFAOYSA-N 0.000 description 1
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- JFWKDYUIJCSHIG-KBXCAEBGSA-N C[C@@H]1OCC(CC2)(CCN2c(nc2C)c(CO)nc2Sc(ccnc2N(C)C)c2Cl)[C@@H]1N Chemical compound C[C@@H]1OCC(CC2)(CCN2c(nc2C)c(CO)nc2Sc(ccnc2N(C)C)c2Cl)[C@@H]1N JFWKDYUIJCSHIG-KBXCAEBGSA-N 0.000 description 1
- GFZDGZWYKUVLMZ-HRAATJIYSA-N C[C@@H]1OCC(CC2)(CCN2c(nc2C)c(CO)nc2Sc(ccnc2OC3CCOCC3)c2Cl)[C@@H]1N Chemical compound C[C@@H]1OCC(CC2)(CCN2c(nc2C)c(CO)nc2Sc(ccnc2OC3CCOCC3)c2Cl)[C@@H]1N GFZDGZWYKUVLMZ-HRAATJIYSA-N 0.000 description 1
- NYULVVAORRYEFY-IFXJQAMLSA-N C[C@@H]1OCC(CC2)(CCN2c(nc2C)c(CO)nc2Sc(ccnc2OC3COC3)c2Cl)[C@@H]1N Chemical compound C[C@@H]1OCC(CC2)(CCN2c(nc2C)c(CO)nc2Sc(ccnc2OC3COC3)c2Cl)[C@@H]1N NYULVVAORRYEFY-IFXJQAMLSA-N 0.000 description 1
- DTZOHZRFTKDHDF-UHFFFAOYSA-N C[O](Cc(cccc1[Zn])c1N)#C Chemical compound C[O](Cc(cccc1[Zn])c1N)#C DTZOHZRFTKDHDF-UHFFFAOYSA-N 0.000 description 1
- JYNXAZHQUABQBS-UHFFFAOYSA-N Cc1cccc(Sc2ncc(NCC3NCCNC3)nc2C)c1C Chemical compound Cc1cccc(Sc2ncc(NCC3NCCNC3)nc2C)c1C JYNXAZHQUABQBS-UHFFFAOYSA-N 0.000 description 1
- HQZBLMNTZQUZGO-UHFFFAOYSA-N Cc1nc(Cl)c(C)c(I)c1 Chemical compound Cc1nc(Cl)c(C)c(I)c1 HQZBLMNTZQUZGO-UHFFFAOYSA-N 0.000 description 1
- DDXSLISYCFTQCY-UHFFFAOYSA-N Cc1nc(Cl)cnc1Br Chemical compound Cc1nc(Cl)cnc1Br DDXSLISYCFTQCY-UHFFFAOYSA-N 0.000 description 1
- PIVSRJIVIYZGRN-MRXNPFEDSA-N Cc1nc(N(CC2)CCC2(CCC2)[C@@H]2N)c(CO)nc1-c(ccc(OC)n1)c1Cl Chemical compound Cc1nc(N(CC2)CCC2(CCC2)[C@@H]2N)c(CO)nc1-c(ccc(OC)n1)c1Cl PIVSRJIVIYZGRN-MRXNPFEDSA-N 0.000 description 1
- FPEYFTNMDRBCHB-QGZVFWFLSA-N Cc1nc(N(CC2)CCC2(CCC2)[C@@H]2N)c(CO)nc1-c1cccc(Cl)c1Cl Chemical compound Cc1nc(N(CC2)CCC2(CCC2)[C@@H]2N)c(CO)nc1-c1cccc(Cl)c1Cl FPEYFTNMDRBCHB-QGZVFWFLSA-N 0.000 description 1
- XJSKNKCPGMSOJY-GHMZBOCLSA-N Cc1nc(N[C@H](CC2)C[C@@H]2N)cnc1Sc1cccc(Cl)c1Cl Chemical compound Cc1nc(N[C@H](CC2)C[C@@H]2N)cnc1Sc1cccc(Cl)c1Cl XJSKNKCPGMSOJY-GHMZBOCLSA-N 0.000 description 1
- QSHVQUKWGCVIAE-UHFFFAOYSA-N Cc1nccc(S)c1Cl Chemical compound Cc1nccc(S)c1Cl QSHVQUKWGCVIAE-UHFFFAOYSA-N 0.000 description 1
- LZYPAUYUKOYCEG-UHFFFAOYSA-N Cc1nccc(Sc(c(I)n2)ncc2Cl)c1Cl Chemical compound Cc1nccc(Sc(c(I)n2)ncc2Cl)c1Cl LZYPAUYUKOYCEG-UHFFFAOYSA-N 0.000 description 1
- KWBMFQGBAMDCGL-UHFFFAOYSA-N Clc1cccc(-c(ncc(Cl)n2)c2I)c1Cl Chemical compound Clc1cccc(-c(ncc(Cl)n2)c2I)c1Cl KWBMFQGBAMDCGL-UHFFFAOYSA-N 0.000 description 1
- YLUKHJSKQPLXRV-MRXNPFEDSA-N N[C@H](CCC1)C1(CC1)CCN1c1cnc(-c(cccc2Cl)c2Cl)c(C#N)n1 Chemical compound N[C@H](CCC1)C1(CC1)CCN1c1cnc(-c(cccc2Cl)c2Cl)c(C#N)n1 YLUKHJSKQPLXRV-MRXNPFEDSA-N 0.000 description 1
- BRPSAOUFIJSKOT-UHFFFAOYSA-N Nc(cccc1Cl)c1Cl Chemical compound Nc(cccc1Cl)c1Cl BRPSAOUFIJSKOT-UHFFFAOYSA-N 0.000 description 1
- LNURMIDMOXCNEH-UHFFFAOYSA-N OC(c1cccc(Br)c1Cl)=O Chemical compound OC(c1cccc(Br)c1Cl)=O LNURMIDMOXCNEH-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—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
- 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
- C07D241/20—Nitrogen atoms
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P35/00—Antineoplastic agents
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- C07D241/10—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
- 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
- C07D241/18—Oxygen or sulfur atoms
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- C07D401/00—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
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- 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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- C07D401/00—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
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—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
- 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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- C07—ORGANIC CHEMISTRY
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- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—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
- C07D403/12—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 linked by a chain containing hetero atoms as chain links
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- C07D405/00—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
- C07D405/14—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 three or more hetero rings
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- C—CHEMISTRY; METALLURGY
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- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
- C07D451/04—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
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- C07D471/00—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
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- C—CHEMISTRY; METALLURGY
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- C—CHEMISTRY; METALLURGY
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- C07D477/00—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring
- C07D477/26—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring with hetero atoms or carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 4
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- C07D491/00—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
- 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
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
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- C07—ORGANIC CHEMISTRY
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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
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
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| AU2023266357A AU2023266357A1 (en) | 2016-07-12 | 2023-11-16 | 2,5-disubstituted 3-methyl pyrazines and 2,5,6-trisubstituted 3-methyl pyrazines as allosteric SHP2 inhibitors |
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