CN108864151A - 杂环胺及其用途 - Google Patents
杂环胺及其用途 Download PDFInfo
- Publication number
- CN108864151A CN108864151A CN201810959036.0A CN201810959036A CN108864151A CN 108864151 A CN108864151 A CN 108864151A CN 201810959036 A CN201810959036 A CN 201810959036A CN 108864151 A CN108864151 A CN 108864151A
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- CN
- China
- Prior art keywords
- base
- pyridine
- methyl
- thiazole
- amino
- 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.)
- Pending
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- -1 heterocyclic amine Chemical class 0.000 title claims abstract description 208
- 150000001875 compounds Chemical class 0.000 claims abstract description 126
- 239000000203 mixture Substances 0.000 claims abstract description 63
- 230000004968 inflammatory condition Effects 0.000 claims abstract description 11
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 344
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 174
- 125000000217 alkyl group Chemical group 0.000 claims description 169
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 159
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims description 114
- 125000003118 aryl group Chemical group 0.000 claims description 104
- ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-aminopyridine Chemical compound NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 claims description 85
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 83
- UHGULLIUJBCTEF-UHFFFAOYSA-N 2-aminobenzothiazole Chemical compound C1=CC=C2SC(N)=NC2=C1 UHGULLIUJBCTEF-UHFFFAOYSA-N 0.000 claims description 78
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical class C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims description 74
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 65
- 229910052736 halogen Inorganic materials 0.000 claims description 64
- 229910052739 hydrogen Inorganic materials 0.000 claims description 61
- 239000001257 hydrogen Substances 0.000 claims description 61
- 239000000126 substance Substances 0.000 claims description 61
- 125000001072 heteroaryl group Chemical group 0.000 claims description 56
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 54
- 150000002431 hydrogen Chemical class 0.000 claims description 51
- 150000002367 halogens Chemical class 0.000 claims description 50
- HFPXKSASPJFSOR-UHFFFAOYSA-N 4-(pyrrolidin-1-ylmethyl)pyridine Chemical compound C=1C=NC=CC=1CN1CCCC1 HFPXKSASPJFSOR-UHFFFAOYSA-N 0.000 claims description 40
- 229940002612 prodrug Drugs 0.000 claims description 31
- 239000000651 prodrug Substances 0.000 claims description 31
- 229910052799 carbon Inorganic materials 0.000 claims description 28
- 150000003839 salts Chemical class 0.000 claims description 24
- 239000003814 drug Substances 0.000 claims description 23
- 150000001408 amides Chemical class 0.000 claims description 22
- 150000002148 esters Chemical class 0.000 claims description 22
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 21
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 21
- 238000002360 preparation method Methods 0.000 claims description 20
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 20
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 18
- 125000003107 substituted aryl group Chemical group 0.000 claims description 18
- 125000002837 carbocyclic group Chemical group 0.000 claims description 13
- 125000002971 oxazolyl group Chemical group 0.000 claims description 13
- 125000003545 alkoxy group Chemical group 0.000 claims description 12
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims description 11
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 11
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 11
- 229940079593 drug Drugs 0.000 claims description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims description 10
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 10
- 125000000304 alkynyl group Chemical group 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
- 125000003342 alkenyl group Chemical group 0.000 claims description 9
- CQABHABFPKXGAF-UHFFFAOYSA-N imidazo[1,2-a]pyridin-2-amine Chemical compound C1=CC=CC2=NC(N)=CN21 CQABHABFPKXGAF-UHFFFAOYSA-N 0.000 claims description 9
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
- 150000003235 pyrrolidines Chemical class 0.000 claims description 8
- 230000019491 signal transduction Effects 0.000 claims description 8
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 claims description 8
- 102000000589 Interleukin-1 Human genes 0.000 claims description 7
- 108010002352 Interleukin-1 Proteins 0.000 claims description 7
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 7
- 201000010099 disease Diseases 0.000 claims description 7
- 150000004820 halides Chemical class 0.000 claims description 7
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims description 7
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 7
- GRHBQAYDJPGGLF-UHFFFAOYSA-N isothiocyanic acid Chemical compound N=C=S GRHBQAYDJPGGLF-UHFFFAOYSA-N 0.000 claims description 7
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 7
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 7
- 201000006417 multiple sclerosis Diseases 0.000 claims description 7
- 230000000241 respiratory effect Effects 0.000 claims description 7
- 208000017520 skin disease Diseases 0.000 claims description 7
- 125000005031 thiocyano group Chemical group S(C#N)* 0.000 claims description 7
- 206010028980 Neoplasm Diseases 0.000 claims description 6
- 208000008589 Obesity Diseases 0.000 claims description 6
- 206010040047 Sepsis Diseases 0.000 claims description 6
- 125000004414 alkyl thio group Chemical group 0.000 claims description 6
- 125000005110 aryl thio group Chemical group 0.000 claims description 6
- 125000004104 aryloxy group Chemical group 0.000 claims description 6
- 201000011510 cancer Diseases 0.000 claims description 6
- 206010012601 diabetes mellitus Diseases 0.000 claims description 6
- 239000003937 drug carrier Substances 0.000 claims description 6
- 230000005764 inhibitory process Effects 0.000 claims description 6
- 235000020824 obesity Nutrition 0.000 claims description 6
- 125000004076 pyridyl group Chemical group 0.000 claims description 6
- 230000004044 response Effects 0.000 claims description 6
- 208000013223 septicemia Diseases 0.000 claims description 6
- KAESVJOAVNADME-UHFFFAOYSA-N 1H-pyrrole Natural products C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 5
- 208000035939 Alveolitis allergic Diseases 0.000 claims description 5
- 206010010741 Conjunctivitis Diseases 0.000 claims description 5
- 206010011224 Cough Diseases 0.000 claims description 5
- 201000004624 Dermatitis Diseases 0.000 claims description 5
- 206010015150 Erythema Diseases 0.000 claims description 5
- 208000027445 Farmer Lung Diseases 0.000 claims description 5
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 5
- 206010028735 Nasal congestion Diseases 0.000 claims description 5
- 108091000080 Phosphotransferase Proteins 0.000 claims description 5
- 208000003251 Pruritus Diseases 0.000 claims description 5
- 201000004681 Psoriasis Diseases 0.000 claims description 5
- 206010040943 Skin Ulcer Diseases 0.000 claims description 5
- 208000025865 Ulcer Diseases 0.000 claims description 5
- 208000024780 Urticaria Diseases 0.000 claims description 5
- 206010046851 Uveitis Diseases 0.000 claims description 5
- 208000006673 asthma Diseases 0.000 claims description 5
- 206010006451 bronchitis Diseases 0.000 claims description 5
- 201000006994 chronic ulcer of skin Diseases 0.000 claims description 5
- 210000004087 cornea Anatomy 0.000 claims description 5
- 231100000321 erythema Toxicity 0.000 claims description 5
- 208000022195 farmer lung disease Diseases 0.000 claims description 5
- 201000010260 leiomyoma Diseases 0.000 claims description 5
- 201000011486 lichen planus Diseases 0.000 claims description 5
- 210000004072 lung Anatomy 0.000 claims description 5
- 201000008482 osteoarthritis Diseases 0.000 claims description 5
- 102000020233 phosphotransferase Human genes 0.000 claims description 5
- 208000015768 polyposis Diseases 0.000 claims description 5
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 claims description 5
- PTMBWNZJOQBTBK-UHFFFAOYSA-N pyridin-4-ylmethanol Chemical compound OCC1=CC=NC=C1 PTMBWNZJOQBTBK-UHFFFAOYSA-N 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 231100000397 ulcer Toxicity 0.000 claims description 5
- VJXRKZJMGVSXPX-UHFFFAOYSA-N 4-ethylpyridine Chemical compound CCC1=CC=NC=C1 VJXRKZJMGVSXPX-UHFFFAOYSA-N 0.000 claims description 4
- 208000022559 Inflammatory bowel disease Diseases 0.000 claims description 4
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 claims description 4
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims description 4
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 4
- 206010039083 rhinitis Diseases 0.000 claims description 4
- RAIPHJJURHTUIC-UHFFFAOYSA-N 1,3-thiazol-2-amine Chemical compound NC1=NC=CS1 RAIPHJJURHTUIC-UHFFFAOYSA-N 0.000 claims description 3
- 206010011686 Cutaneous vasculitis Diseases 0.000 claims description 3
- 239000005864 Sulphur Substances 0.000 claims description 3
- 229910021529 ammonia Inorganic materials 0.000 claims description 3
- 150000002576 ketones Chemical class 0.000 claims description 3
- 150000003053 piperidines Chemical class 0.000 claims description 3
- 125000002098 pyridazinyl group Chemical group 0.000 claims description 3
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims description 2
- 206010003246 arthritis Diseases 0.000 claims description 2
- 150000002460 imidazoles Chemical class 0.000 claims description 2
- 239000008194 pharmaceutical composition Substances 0.000 claims description 2
- 150000003217 pyrazoles Chemical class 0.000 claims description 2
- 150000003222 pyridines Chemical class 0.000 claims description 2
- 150000004040 pyrrolidinones Chemical class 0.000 claims description 2
- XKVUYEYANWFIJX-UHFFFAOYSA-N 5-methyl-1h-pyrazole Chemical class CC1=CC=NN1 XKVUYEYANWFIJX-UHFFFAOYSA-N 0.000 claims 84
- FDPIMTJIUBPUKL-UHFFFAOYSA-N dimethylacetone Natural products CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 claims 68
- BMEMBBFDTYHTLH-UHFFFAOYSA-N 1-(2-methoxyethyl)piperazine Chemical compound COCCN1CCNCC1 BMEMBBFDTYHTLH-UHFFFAOYSA-N 0.000 claims 21
- WYRRTJKOMZONQO-UHFFFAOYSA-N 1,3-benzothiazole-6-carbonitrile Chemical compound N#CC1=CC=C2N=CSC2=C1 WYRRTJKOMZONQO-UHFFFAOYSA-N 0.000 claims 18
- ZZAKLGGGMWORRT-UHFFFAOYSA-N 1-methylsulfonylpiperazine Chemical compound CS(=O)(=O)N1CCNCC1 ZZAKLGGGMWORRT-UHFFFAOYSA-N 0.000 claims 18
- 125000000437 thiazol-2-yl group Chemical group [H]C1=C([H])N=C(*)S1 0.000 claims 15
- NXUBYNYAZDYXBU-UHFFFAOYSA-N 5-pyridin-4-yl-1,3-thiazole Chemical compound S1C=NC=C1C1=CC=NC=C1 NXUBYNYAZDYXBU-UHFFFAOYSA-N 0.000 claims 12
- 235000019441 ethanol Nutrition 0.000 claims 12
- RDRCCJPEJDWSRJ-UHFFFAOYSA-N pyridine;1h-pyrrole Chemical compound C=1C=CNC=1.C1=CC=NC=C1 RDRCCJPEJDWSRJ-UHFFFAOYSA-N 0.000 claims 12
- BWRWNUQAQPAYCK-UHFFFAOYSA-N 3-methoxypyrrolidine Chemical compound COC1CCNC1 BWRWNUQAQPAYCK-UHFFFAOYSA-N 0.000 claims 11
- QARVLSVVCXYDNA-UHFFFAOYSA-N bromobenzene Chemical compound BrC1=CC=CC=C1 QARVLSVVCXYDNA-UHFFFAOYSA-N 0.000 claims 9
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 claims 8
- QJWQYVJVCXMTJP-UHFFFAOYSA-N 4-pyridin-4-ylmorpholine Chemical compound C1COCCN1C1=CC=NC=C1 QJWQYVJVCXMTJP-UHFFFAOYSA-N 0.000 claims 8
- HVZJSUVDFMFZCP-UHFFFAOYSA-N 1-(2-propan-2-yloxyethyl)piperazine Chemical compound CC(C)OCCN1CCNCC1 HVZJSUVDFMFZCP-UHFFFAOYSA-N 0.000 claims 6
- PYSUBPCPJRBSGH-UHFFFAOYSA-N 1-(3,3,3-trifluoropropyl)piperazine Chemical compound FC(F)(F)CCN1CCNCC1 PYSUBPCPJRBSGH-UHFFFAOYSA-N 0.000 claims 6
- NGHHVCGBOOCIBY-UHFFFAOYSA-N 1-methyl-4-pyridin-4-ylpiperazine Chemical compound C1CN(C)CCN1C1=CC=NC=C1 NGHHVCGBOOCIBY-UHFFFAOYSA-N 0.000 claims 6
- RNFJZUCGOOPTKV-UHFFFAOYSA-N 4-(propoxymethyl)pyridine Chemical compound CCCOCC1=CC=NC=C1 RNFJZUCGOOPTKV-UHFFFAOYSA-N 0.000 claims 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 6
- VJOFNWDVXXUHAG-UHFFFAOYSA-N n,n-dimethyl-1-pyridin-4-ylmethanamine Chemical compound CN(C)CC1=CC=NC=C1 VJOFNWDVXXUHAG-UHFFFAOYSA-N 0.000 claims 6
- XWINCPYLXQTPQV-UHFFFAOYSA-N piperazine Chemical compound C1CNCCN1.C1CNCCN1 XWINCPYLXQTPQV-UHFFFAOYSA-N 0.000 claims 6
- AFEPWWJCYWMEHF-UHFFFAOYSA-N 2-methoxy-1-(4-pyridin-2-ylpiperazin-1-yl)ethanone Chemical class C1CN(C(=O)COC)CCN1C1=CC=CC=N1 AFEPWWJCYWMEHF-UHFFFAOYSA-N 0.000 claims 5
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims 5
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims 5
- UTCSSFWDNNEEBH-UHFFFAOYSA-N imidazo[1,2-a]pyridine Chemical compound C1=CC=CC2=NC=CN21 UTCSSFWDNNEEBH-UHFFFAOYSA-N 0.000 claims 5
- DNBWGFKLIBQQSL-UHFFFAOYSA-N n-methyl-1-pyridin-4-ylmethanamine Chemical compound CNCC1=CC=NC=C1 DNBWGFKLIBQQSL-UHFFFAOYSA-N 0.000 claims 5
- TXQWFIVRZNOPCK-UHFFFAOYSA-N pyridin-4-ylmethanamine Chemical compound NCC1=CC=NC=C1 TXQWFIVRZNOPCK-UHFFFAOYSA-N 0.000 claims 5
- UZASMYQTKALYAA-UHFFFAOYSA-N 1-benzothiophene 1H-pyrrole Chemical class N1C=CC=C1.S1C=CC2=C1C=CC=C2 UZASMYQTKALYAA-UHFFFAOYSA-N 0.000 claims 4
- RABBMOYULJIAFU-UHFFFAOYSA-N 1h-pyrrole;thiophene Chemical class C=1C=CNC=1.C=1C=CSC=1 RABBMOYULJIAFU-UHFFFAOYSA-N 0.000 claims 4
- YXPHKMZYEBWDQO-UHFFFAOYSA-N 2-methoxy-1-piperazin-1-ylethanone Chemical compound COCC(=O)N1CCNCC1 YXPHKMZYEBWDQO-UHFFFAOYSA-N 0.000 claims 4
- PSZFGHUEAYIHLB-UHFFFAOYSA-N 2-methyl-1-methylsulfonylpiperazine Chemical compound CC1CNCCN1S(C)(=O)=O PSZFGHUEAYIHLB-UHFFFAOYSA-N 0.000 claims 4
- AHXSBNBPHMFXGQ-UHFFFAOYSA-N 3-methyl-1-methylsulfonylpiperazine Chemical compound CC1CN(S(C)(=O)=O)CCN1 AHXSBNBPHMFXGQ-UHFFFAOYSA-N 0.000 claims 4
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 4
- GTPXCGRVFBUXQC-UHFFFAOYSA-N 4-(piperidin-1-ylmethyl)pyridine Chemical compound C=1C=NC=CC=1CN1CCCCC1 GTPXCGRVFBUXQC-UHFFFAOYSA-N 0.000 claims 4
- 125000002619 bicyclic group Chemical group 0.000 claims 4
- 229960005206 pyrazinamide Drugs 0.000 claims 4
- IPEHBUMCGVEMRF-UHFFFAOYSA-N pyrazinecarboxamide Chemical compound NC(=O)C1=CN=CC=N1 IPEHBUMCGVEMRF-UHFFFAOYSA-N 0.000 claims 4
- XZYLSJPLCLKCMR-UHFFFAOYSA-N 1-(pyridin-4-ylmethyl)piperazine Chemical compound C=1C=NC=CC=1CN1CCNCC1 XZYLSJPLCLKCMR-UHFFFAOYSA-N 0.000 claims 3
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 3
- 125000004575 3-pyrrolidinyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 3
- ARBNXCZDMDQDTJ-UHFFFAOYSA-N 4-(azetidin-1-ylmethyl)pyridine Chemical compound N1=CC=C(C=C1)CN1CCC1 ARBNXCZDMDQDTJ-UHFFFAOYSA-N 0.000 claims 3
- NAMVLAMKNUHHCR-UHFFFAOYSA-N 6-pyridin-4-ylimidazo[1,2-a]pyridine Chemical compound C1=CC2=NC=CN2C=C1C1=CC=NC=C1 NAMVLAMKNUHHCR-UHFFFAOYSA-N 0.000 claims 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims 3
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- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 2
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- OIVXYLRFBFGUGR-UHFFFAOYSA-N 6-pyridin-3-ylimidazo[1,2-a]pyridine Chemical compound C1=CC2=NC=CN2C=C1C1=CC=CN=C1 OIVXYLRFBFGUGR-UHFFFAOYSA-N 0.000 claims 2
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 239000011737 fluorine Substances 0.000 claims 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N formamide Substances NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 claims 2
- LRJOKNYELSECDZ-UHFFFAOYSA-N imidazo[1,2-a]pyridine-6-carbonitrile Chemical compound C1=C(C#N)C=CC2=NC=CN21 LRJOKNYELSECDZ-UHFFFAOYSA-N 0.000 claims 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims 2
- GTCAXTIRRLKXRU-UHFFFAOYSA-N methyl carbamate Chemical compound COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 claims 2
- YESFJLBISUFNFW-UHFFFAOYSA-N n,n-dimethyl-3-pyridin-4-ylpropanamide Chemical compound CN(C)C(=O)CCC1=CC=NC=C1 YESFJLBISUFNFW-UHFFFAOYSA-N 0.000 claims 2
- RFGXUQGONLWUAI-UHFFFAOYSA-N n-(4-piperazin-1-ylpyridin-2-yl)-6-pyridin-4-yl-1,3-benzothiazol-2-amine Chemical compound C1CNCCN1C1=CC=NC(NC=2SC3=CC(=CC=C3N=2)C=2C=CN=CC=2)=C1 RFGXUQGONLWUAI-UHFFFAOYSA-N 0.000 claims 2
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Classifications
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- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
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- C07D417/00—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
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- Nitrogen Condensed Heterocyclic Rings (AREA)
- Thiazole And Isothizaole Compounds (AREA)
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| WO2013169382A1 (en) * | 2012-05-07 | 2013-11-14 | DePuy Synthes Products, LLC | Methods and devices for treating intervertebral disc disease |
| US9546153B2 (en) * | 2012-11-08 | 2017-01-17 | Bristol-Myers Squibb Company | Bicyclic heterocycle substituted pyridyl compounds useful as kinase modulators |
| EP3049086A4 (en) * | 2013-09-27 | 2017-02-22 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
| CN106061480B (zh) * | 2013-12-30 | 2020-02-28 | 莱福斯希医药公司 | 治疗性抑制性化合物 |
| HRP20181795T1 (hr) * | 2014-01-13 | 2019-01-25 | Aurigene Discovery Technologies Limited | Biciklički heterociklilni derivati kao inhibitori irak4 |
| PL3286181T3 (pl) | 2015-04-22 | 2021-08-02 | Rigel Pharmaceuticals, Inc. | Związki pirazolowe oraz sposób wytwarzania i zastosowania tych związków |
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