JP5815029B2 - カルシウムチャネル遮断薬としてのテトラゾール化合物 - Google Patents
カルシウムチャネル遮断薬としてのテトラゾール化合物 Download PDFInfo
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- JP5815029B2 JP5815029B2 JP2013517548A JP2013517548A JP5815029B2 JP 5815029 B2 JP5815029 B2 JP 5815029B2 JP 2013517548 A JP2013517548 A JP 2013517548A JP 2013517548 A JP2013517548 A JP 2013517548A JP 5815029 B2 JP5815029 B2 JP 5815029B2
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- Japan
- Prior art keywords
- methyl
- compound
- tetrazol
- trifluoromethyl
- phenyl
- 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.)
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- -1 Tetrazole compounds Chemical class 0.000 title claims description 37
- 229940127291 Calcium channel antagonist Drugs 0.000 title description 2
- 239000000480 calcium channel blocker Substances 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 372
- 229910052739 hydrogen Inorganic materials 0.000 claims description 130
- 239000001257 hydrogen Substances 0.000 claims description 129
- 125000000217 alkyl group Chemical group 0.000 claims description 104
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 94
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 79
- 125000004122 cyclic group Chemical group 0.000 claims description 77
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 65
- 150000003839 salts Chemical class 0.000 claims description 64
- 150000002431 hydrogen Chemical class 0.000 claims description 59
- 229910052757 nitrogen Inorganic materials 0.000 claims description 59
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 58
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 51
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 46
- 125000000623 heterocyclic group Chemical group 0.000 claims description 44
- 125000002950 monocyclic group Chemical group 0.000 claims description 42
- 125000001424 substituent group Chemical group 0.000 claims description 40
- 208000002193 Pain Diseases 0.000 claims description 39
- 125000002911 monocyclic heterocycle group Chemical group 0.000 claims description 38
- 229910052736 halogen Inorganic materials 0.000 claims description 37
- 150000002367 halogens Chemical class 0.000 claims description 37
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 claims description 34
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 23
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 23
- 125000004193 piperazinyl group Chemical group 0.000 claims description 22
- DIQOUXNTSMWQSA-UHFFFAOYSA-N 2-oxa-5-azabicyclo[2.2.1]heptane Chemical group C1OC2CNC1C2 DIQOUXNTSMWQSA-UHFFFAOYSA-N 0.000 claims description 18
- 239000003814 drug Substances 0.000 claims description 18
- 230000002265 prevention Effects 0.000 claims description 18
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 11
- WVOPWZRQDAOXEB-UHFFFAOYSA-N 4-[5-[(3,4-dimethylpiperazin-1-yl)methyl]tetrazol-1-yl]benzonitrile;dihydrochloride Chemical compound Cl.Cl.C1CN(C)C(C)CN1CC1=NN=NN1C1=CC=C(C#N)C=C1 WVOPWZRQDAOXEB-UHFFFAOYSA-N 0.000 claims description 11
- LBOGIHKNXFTJEK-UHFFFAOYSA-N 4-[5-[(4-methylpiperazin-1-yl)methyl]tetrazol-1-yl]benzonitrile;dihydrochloride Chemical compound Cl.Cl.C1CN(C)CCN1CC1=NN=NN1C1=CC=C(C#N)C=C1 LBOGIHKNXFTJEK-UHFFFAOYSA-N 0.000 claims description 11
- HMCUJCQGYSFLJS-UHFFFAOYSA-N 4-[5-[(4-propan-2-ylpiperazin-1-yl)methyl]tetrazol-1-yl]benzonitrile;dihydrochloride Chemical compound Cl.Cl.C1CN(C(C)C)CCN1CC1=NN=NN1C1=CC=C(C#N)C=C1 HMCUJCQGYSFLJS-UHFFFAOYSA-N 0.000 claims description 11
- 239000008194 pharmaceutical composition Substances 0.000 claims description 11
- 238000002560 therapeutic procedure Methods 0.000 claims description 10
- 206010065390 Inflammatory pain Diseases 0.000 claims description 9
- 208000004296 neuralgia Diseases 0.000 claims description 9
- AAKSTVXHRNNNGZ-UHFFFAOYSA-N 4-[[1-(4-chlorophenyl)tetrazol-5-yl]methyl]morpholine Chemical compound C1=CC(Cl)=CC=C1N1C(CN2CCOCC2)=NN=N1 AAKSTVXHRNNNGZ-UHFFFAOYSA-N 0.000 claims description 8
- GYHNTOWCMLSOGI-UHFFFAOYSA-N 4-[[1-[3-(trifluoromethyl)phenyl]tetrazol-5-yl]methyl]morpholine Chemical compound FC(F)(F)C1=CC=CC(N2C(=NN=N2)CN2CCOCC2)=C1 GYHNTOWCMLSOGI-UHFFFAOYSA-N 0.000 claims description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
- 208000021722 neuropathic pain Diseases 0.000 claims description 8
- 208000019695 Migraine disease Diseases 0.000 claims description 7
- 206010027599 migraine Diseases 0.000 claims description 7
- GOZVGSRNTQFFKY-UHFFFAOYSA-N 4-[[1-[3-(trifluoromethyl)phenyl]tetrazol-5-yl]methyl]morpholine;hydrochloride Chemical compound Cl.FC(F)(F)C1=CC=CC(N2C(=NN=N2)CN2CCOCC2)=C1 GOZVGSRNTQFFKY-UHFFFAOYSA-N 0.000 claims description 6
- 229940126639 Compound 33 Drugs 0.000 claims description 6
- PNUZDKCDAWUEGK-CYZMBNFOSA-N Sitafloxacin Chemical compound C([C@H]1N)N(C=2C(=C3C(C(C(C(O)=O)=CN3[C@H]3[C@H](C3)F)=O)=CC=2F)Cl)CC11CC1 PNUZDKCDAWUEGK-CYZMBNFOSA-N 0.000 claims description 6
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
- 125000001246 bromo group Chemical group Br* 0.000 claims description 5
- 125000001153 fluoro group Chemical group F* 0.000 claims description 5
- UAOUIVVJBYDFKD-XKCDOFEDSA-N (1R,9R,10S,11R,12R,15S,18S,21R)-10,11,21-trihydroxy-8,8-dimethyl-14-methylidene-4-(prop-2-enylamino)-20-oxa-5-thia-3-azahexacyclo[9.7.2.112,15.01,9.02,6.012,18]henicosa-2(6),3-dien-13-one Chemical compound C([C@@H]1[C@@H](O)[C@@]23C(C1=C)=O)C[C@H]2[C@]12C(N=C(NCC=C)S4)=C4CC(C)(C)[C@H]1[C@H](O)[C@]3(O)OC2 UAOUIVVJBYDFKD-XKCDOFEDSA-N 0.000 claims description 4
- ONLZASKPAVQAMQ-UHFFFAOYSA-N 1-[[1-(4-chlorophenyl)tetrazol-5-yl]methyl]-4-ethylsulfonylpiperazine Chemical compound C1CN(S(=O)(=O)CC)CCN1CC1=NN=NN1C1=CC=C(Cl)C=C1 ONLZASKPAVQAMQ-UHFFFAOYSA-N 0.000 claims description 4
- UNGDBWBPQGCVTF-UHFFFAOYSA-N 1-[[1-(4-chlorophenyl)tetrazol-5-yl]methyl]-4-methylsulfonylpiperazine Chemical compound C1CN(S(=O)(=O)C)CCN1CC1=NN=NN1C1=CC=C(Cl)C=C1 UNGDBWBPQGCVTF-UHFFFAOYSA-N 0.000 claims description 4
- FEHRBCZAIUPUGI-UHFFFAOYSA-N 1-[[1-(4-chlorophenyl)tetrazol-5-yl]methyl]-4-propylsulfonylpiperazine Chemical compound C1CN(S(=O)(=O)CCC)CCN1CC1=NN=NN1C1=CC=C(Cl)C=C1 FEHRBCZAIUPUGI-UHFFFAOYSA-N 0.000 claims description 4
- ALKNYGMLUFOYEJ-UHFFFAOYSA-N 1-ethylsulfonyl-4-[[1-[3-(trifluoromethyl)phenyl]tetrazol-5-yl]methyl]piperazine Chemical compound C1CN(S(=O)(=O)CC)CCN1CC1=NN=NN1C1=CC=CC(C(F)(F)F)=C1 ALKNYGMLUFOYEJ-UHFFFAOYSA-N 0.000 claims description 4
- QBWKPGNFQQJGFY-QLFBSQMISA-N 3-[(1r)-1-[(2r,6s)-2,6-dimethylmorpholin-4-yl]ethyl]-n-[6-methyl-3-(1h-pyrazol-4-yl)imidazo[1,2-a]pyrazin-8-yl]-1,2-thiazol-5-amine Chemical compound N1([C@H](C)C2=NSC(NC=3C4=NC=C(N4C=C(C)N=3)C3=CNN=C3)=C2)C[C@H](C)O[C@H](C)C1 QBWKPGNFQQJGFY-QLFBSQMISA-N 0.000 claims description 4
- BEVYTMYRNCVFLV-UHFFFAOYSA-N 3-methyl-4-[[1-[3-(trifluoromethyl)phenyl]tetrazol-5-yl]methyl]piperazin-2-one Chemical compound C1CNC(=O)C(C)N1CC1=NN=NN1C1=CC=CC(C(F)(F)F)=C1 BEVYTMYRNCVFLV-UHFFFAOYSA-N 0.000 claims description 4
- MZTTVNJYLQTXBP-UHFFFAOYSA-N 4-[5-[(3,3-dimethylmorpholin-4-yl)methyl]tetrazol-1-yl]benzonitrile Chemical compound CC1(C)COCCN1CC1=NN=NN1C1=CC=C(C#N)C=C1 MZTTVNJYLQTXBP-UHFFFAOYSA-N 0.000 claims description 4
- VPHLOFBKQMMHCQ-RYUDHWBXSA-N 4-[5-[[(1s,4s)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl]methyl]tetrazol-1-yl]-2-(trifluoromethyl)benzonitrile Chemical compound C([C@]1(OC[C@]2([H])C1)[H])N2CC1=NN=NN1C1=CC=C(C#N)C(C(F)(F)F)=C1 VPHLOFBKQMMHCQ-RYUDHWBXSA-N 0.000 claims description 4
- ATERIOPVZQLFSL-SNVBAGLBSA-N 4-[5-[[(3r)-3-methylmorpholin-4-yl]methyl]tetrazol-1-yl]-2-(trifluoromethyl)benzonitrile Chemical compound C[C@@H]1COCCN1CC1=NN=NN1C1=CC=C(C#N)C(C(F)(F)F)=C1 ATERIOPVZQLFSL-SNVBAGLBSA-N 0.000 claims description 4
- DXVLZRVZWXLZEZ-UHFFFAOYSA-N 4-[[1-(3,4-dichlorophenyl)tetrazol-5-yl]methyl]morpholine Chemical compound C1=C(Cl)C(Cl)=CC=C1N1C(CN2CCOCC2)=NN=N1 DXVLZRVZWXLZEZ-UHFFFAOYSA-N 0.000 claims description 4
- PSLUFJFHTBIXMW-WYEYVKMPSA-N [(3r,4ar,5s,6s,6as,10s,10ar,10bs)-3-ethenyl-10,10b-dihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-6-(2-pyridin-2-ylethylcarbamoyloxy)-5,6,6a,8,9,10-hexahydro-2h-benzo[f]chromen-5-yl] acetate Chemical compound O([C@@H]1[C@@H]([C@]2(O[C@](C)(CC(=O)[C@]2(O)[C@@]2(C)[C@@H](O)CCC(C)(C)[C@@H]21)C=C)C)OC(=O)C)C(=O)NCCC1=CC=CC=N1 PSLUFJFHTBIXMW-WYEYVKMPSA-N 0.000 claims description 4
- 229940125846 compound 25 Drugs 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 125000004043 oxo group Chemical group O=* 0.000 claims description 4
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 4
- POMFSMHRMSLPET-JQWIXIFHSA-N (1s,4s)-2-[[1-[4-(trifluoromethyl)phenyl]tetrazol-5-yl]methyl]-2,5-diazabicyclo[2.2.1]heptane Chemical compound C([C@]1(NC[C@]2([H])C1)[H])N2CC1=NN=NN1C1=CC=C(C(F)(F)F)C=C1 POMFSMHRMSLPET-JQWIXIFHSA-N 0.000 claims description 3
- VIJSPAIQWVPKQZ-BLECARSGSA-N (2s)-2-[[(2s)-2-[[(2s)-2-[[(2s)-2-[[(2s)-2-[[(2s)-2-acetamido-5-(diaminomethylideneamino)pentanoyl]amino]-4-methylpentanoyl]amino]-4,4-dimethylpentanoyl]amino]-4-methylpentanoyl]amino]propanoyl]amino]-5-(diaminomethylideneamino)pentanoic acid Chemical compound NC(=N)NCCC[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCNC(N)=N)NC(C)=O VIJSPAIQWVPKQZ-BLECARSGSA-N 0.000 claims description 3
- MPDDTAJMJCESGV-CTUHWIOQSA-M (3r,5r)-7-[2-(4-fluorophenyl)-5-[methyl-[(1r)-1-phenylethyl]carbamoyl]-4-propan-2-ylpyrazol-3-yl]-3,5-dihydroxyheptanoate Chemical compound C1([C@@H](C)N(C)C(=O)C2=NN(C(CC[C@@H](O)C[C@@H](O)CC([O-])=O)=C2C(C)C)C=2C=CC(F)=CC=2)=CC=CC=C1 MPDDTAJMJCESGV-CTUHWIOQSA-M 0.000 claims description 3
- YQOLEILXOBUDMU-KRWDZBQOSA-N (4R)-5-[(6-bromo-3-methyl-2-pyrrolidin-1-ylquinoline-4-carbonyl)amino]-4-(2-chlorophenyl)pentanoic acid Chemical compound CC1=C(C2=C(C=CC(=C2)Br)N=C1N3CCCC3)C(=O)NC[C@H](CCC(=O)O)C4=CC=CC=C4Cl YQOLEILXOBUDMU-KRWDZBQOSA-N 0.000 claims description 3
- XXVLFQVLMTUGNV-UHFFFAOYSA-N 1-(4-chlorophenyl)-5-(pyrrolidin-1-ylmethyl)tetrazole Chemical compound C1=CC(Cl)=CC=C1N1C(CN2CCCC2)=NN=N1 XXVLFQVLMTUGNV-UHFFFAOYSA-N 0.000 claims description 3
- AGMZBXBHWYHIFZ-UHFFFAOYSA-N 1-[[1-(4-chlorophenyl)tetrazol-5-yl]methyl]-4-methylpiperazine Chemical compound C1CN(C)CCN1CC1=NN=NN1C1=CC=C(Cl)C=C1 AGMZBXBHWYHIFZ-UHFFFAOYSA-N 0.000 claims description 3
- VCOKNESLRBSXPG-UHFFFAOYSA-N 1-[[1-(4-chlorophenyl)tetrazol-5-yl]methyl]azepane Chemical compound C1=CC(Cl)=CC=C1N1C(CN2CCCCCC2)=NN=N1 VCOKNESLRBSXPG-UHFFFAOYSA-N 0.000 claims description 3
- OMBVIHTZXXZALD-UHFFFAOYSA-N 1-[[1-(4-chlorophenyl)tetrazol-5-yl]methyl]piperidine Chemical compound C1=CC(Cl)=CC=C1N1C(CN2CCCCC2)=NN=N1 OMBVIHTZXXZALD-UHFFFAOYSA-N 0.000 claims description 3
- UVRBVWDQUHKUCC-UHFFFAOYSA-N 3,3-dimethyl-4-[[1-[3-(trifluoromethyl)phenyl]tetrazol-5-yl]methyl]morpholine Chemical compound CC1(C)COCCN1CC1=NN=NN1C1=CC=CC(C(F)(F)F)=C1 UVRBVWDQUHKUCC-UHFFFAOYSA-N 0.000 claims description 3
- VMUQCIPDFFGRIW-UHFFFAOYSA-N 4-[1-[1-[4-(trifluoromethyl)phenyl]tetrazol-5-yl]ethyl]morpholine Chemical compound N=1N=NN(C=2C=CC(=CC=2)C(F)(F)F)C=1C(C)N1CCOCC1 VMUQCIPDFFGRIW-UHFFFAOYSA-N 0.000 claims description 3
- WYFCZWSWFGJODV-MIANJLSGSA-N 4-[[(1s)-2-[(e)-3-[3-chloro-2-fluoro-6-(tetrazol-1-yl)phenyl]prop-2-enoyl]-5-(4-methyl-2-oxopiperazin-1-yl)-3,4-dihydro-1h-isoquinoline-1-carbonyl]amino]benzoic acid Chemical compound O=C1CN(C)CCN1C1=CC=CC2=C1CCN(C(=O)\C=C\C=1C(=CC=C(Cl)C=1F)N1N=NN=C1)[C@@H]2C(=O)NC1=CC=C(C(O)=O)C=C1 WYFCZWSWFGJODV-MIANJLSGSA-N 0.000 claims description 3
- CYKLPPRKXZMHOF-UHFFFAOYSA-N 4-[[1-[4-(trifluoromethyl)phenyl]tetrazol-5-yl]methyl]morpholine Chemical compound C1=CC(C(F)(F)F)=CC=C1N1C(CN2CCOCC2)=NN=N1 CYKLPPRKXZMHOF-UHFFFAOYSA-N 0.000 claims description 3
- 229940126214 compound 3 Drugs 0.000 claims description 3
- 229940125844 compound 46 Drugs 0.000 claims description 3
- ASGMFNBUXDJWJJ-JLCFBVMHSA-N (1R,3R)-3-[[3-bromo-1-[4-(5-methyl-1,3,4-thiadiazol-2-yl)phenyl]pyrazolo[3,4-d]pyrimidin-6-yl]amino]-N,1-dimethylcyclopentane-1-carboxamide Chemical compound BrC1=NN(C2=NC(=NC=C21)N[C@H]1C[C@@](CC1)(C(=O)NC)C)C1=CC=C(C=C1)C=1SC(=NN=1)C ASGMFNBUXDJWJJ-JLCFBVMHSA-N 0.000 claims description 2
- AOSZTAHDEDLTLQ-AZKQZHLXSA-N (1S,2S,4R,8S,9S,11S,12R,13S,19S)-6-[(3-chlorophenyl)methyl]-12,19-difluoro-11-hydroxy-8-(2-hydroxyacetyl)-9,13-dimethyl-6-azapentacyclo[10.8.0.02,9.04,8.013,18]icosa-14,17-dien-16-one Chemical compound C([C@@H]1C[C@H]2[C@H]3[C@]([C@]4(C=CC(=O)C=C4[C@@H](F)C3)C)(F)[C@@H](O)C[C@@]2([C@@]1(C1)C(=O)CO)C)N1CC1=CC=CC(Cl)=C1 AOSZTAHDEDLTLQ-AZKQZHLXSA-N 0.000 claims description 2
- ABJSOROVZZKJGI-OCYUSGCXSA-N (1r,2r,4r)-2-(4-bromophenyl)-n-[(4-chlorophenyl)-(2-fluoropyridin-4-yl)methyl]-4-morpholin-4-ylcyclohexane-1-carboxamide Chemical compound C1=NC(F)=CC(C(NC(=O)[C@H]2[C@@H](C[C@@H](CC2)N2CCOCC2)C=2C=CC(Br)=CC=2)C=2C=CC(Cl)=CC=2)=C1 ABJSOROVZZKJGI-OCYUSGCXSA-N 0.000 claims description 2
- SZUVGFMDDVSKSI-WIFOCOSTSA-N (1s,2s,3s,5r)-1-(carboxymethyl)-3,5-bis[(4-phenoxyphenyl)methyl-propylcarbamoyl]cyclopentane-1,2-dicarboxylic acid Chemical compound O=C([C@@H]1[C@@H]([C@](CC(O)=O)([C@H](C(=O)N(CCC)CC=2C=CC(OC=3C=CC=CC=3)=CC=2)C1)C(O)=O)C(O)=O)N(CCC)CC(C=C1)=CC=C1OC1=CC=CC=C1 SZUVGFMDDVSKSI-WIFOCOSTSA-N 0.000 claims description 2
- IAHWZWWAHLCNMI-YYLIZZNMSA-N (1s,4s)-2-propan-2-yl-5-[[1-[4-(trifluoromethyl)phenyl]tetrazol-5-yl]methyl]-2,5-diazabicyclo[2.2.1]heptane;hydrochloride Chemical compound Cl.C([C@]1(N(C(C)C)C[C@@]2(C1)[H])[H])N2CC1=NN=NN1C1=CC=C(C(F)(F)F)C=C1 IAHWZWWAHLCNMI-YYLIZZNMSA-N 0.000 claims description 2
- REHXHVPNTVPDAJ-FXMYHANSSA-N (1s,4s)-5-[[1-[4-(trifluoromethyl)phenyl]tetrazol-5-yl]methyl]-2-oxa-5-azabicyclo[2.2.1]heptane;hydrochloride Chemical compound Cl.C([C@]1(OC[C@]2([H])C1)[H])N2CC1=NN=NN1C1=CC=C(C(F)(F)F)C=C1 REHXHVPNTVPDAJ-FXMYHANSSA-N 0.000 claims description 2
- GHYOCDFICYLMRF-UTIIJYGPSA-N (2S,3R)-N-[(2S)-3-(cyclopenten-1-yl)-1-[(2R)-2-methyloxiran-2-yl]-1-oxopropan-2-yl]-3-hydroxy-3-(4-methoxyphenyl)-2-[[(2S)-2-[(2-morpholin-4-ylacetyl)amino]propanoyl]amino]propanamide Chemical compound C1(=CCCC1)C[C@@H](C(=O)[C@@]1(OC1)C)NC([C@H]([C@@H](C1=CC=C(C=C1)OC)O)NC([C@H](C)NC(CN1CCOCC1)=O)=O)=O GHYOCDFICYLMRF-UTIIJYGPSA-N 0.000 claims description 2
- IUSARDYWEPUTPN-OZBXUNDUSA-N (2r)-n-[(2s,3r)-4-[[(4s)-6-(2,2-dimethylpropyl)spiro[3,4-dihydropyrano[2,3-b]pyridine-2,1'-cyclobutane]-4-yl]amino]-3-hydroxy-1-[3-(1,3-thiazol-2-yl)phenyl]butan-2-yl]-2-methoxypropanamide Chemical compound C([C@H](NC(=O)[C@@H](C)OC)[C@H](O)CN[C@@H]1C2=CC(CC(C)(C)C)=CN=C2OC2(CCC2)C1)C(C=1)=CC=CC=1C1=NC=CS1 IUSARDYWEPUTPN-OZBXUNDUSA-N 0.000 claims description 2
- YJLIKUSWRSEPSM-WGQQHEPDSA-N (2r,3r,4s,5r)-2-[6-amino-8-[(4-phenylphenyl)methylamino]purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol Chemical compound C=1C=C(C=2C=CC=CC=2)C=CC=1CNC1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O YJLIKUSWRSEPSM-WGQQHEPDSA-N 0.000 claims description 2
- UNQBXKKMTCOLJT-TXEJJXNPSA-N (2r,6s)-2,6-dimethyl-4-[2-[1-[4-(trifluoromethyl)phenyl]tetrazol-5-yl]ethyl]morpholine Chemical compound C1[C@@H](C)O[C@@H](C)CN1CCC1=NN=NN1C1=CC=C(C(F)(F)F)C=C1 UNQBXKKMTCOLJT-TXEJJXNPSA-N 0.000 claims description 2
- LVKSSIPJOACEHV-TXEJJXNPSA-N (2r,6s)-2,6-dimethyl-4-[[1-(4-methylsulfanylphenyl)tetrazol-5-yl]methyl]morpholine Chemical compound C1=CC(SC)=CC=C1N1C(CN2C[C@@H](C)O[C@@H](C)C2)=NN=N1 LVKSSIPJOACEHV-TXEJJXNPSA-N 0.000 claims description 2
- RAJLQXMVZULAHM-IWKKHLOMSA-N (2r,6s)-4-[[1-(4-bromo-2-methylphenyl)tetrazol-5-yl]methyl]-2,6-dimethylmorpholine;hydrochloride Chemical compound Cl.C1[C@@H](C)O[C@@H](C)CN1CC1=NN=NN1C1=CC=C(Br)C=C1C RAJLQXMVZULAHM-IWKKHLOMSA-N 0.000 claims description 2
- JKUUUVMWLJAXPZ-PHIMTYICSA-N (2r,6s)-4-[[1-(4-chlorophenyl)tetrazol-5-yl]methyl]-2,6-dimethylmorpholine Chemical compound C1[C@@H](C)O[C@@H](C)CN1CC1=NN=NN1C1=CC=C(Cl)C=C1 JKUUUVMWLJAXPZ-PHIMTYICSA-N 0.000 claims description 2
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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
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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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| US61/362,712 | 2010-07-09 | ||
| PCT/GB2011/051276 WO2012004604A1 (en) | 2010-07-09 | 2011-07-08 | Tetrazole compounds as calcium channel blockers |
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| JP2013535414A JP2013535414A (ja) | 2013-09-12 |
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| TW201416348A (zh) * | 2012-08-29 | 2014-05-01 | Gruenenthal Chemie | 以氟甲基取代之吡咯甲醯胺 |
| CN103570584B (zh) * | 2013-11-04 | 2015-01-07 | 上海应用技术学院 | 一种取代苯甲脒类化合物的合成方法 |
| CN103553967B (zh) * | 2013-11-04 | 2015-02-18 | 上海应用技术学院 | 一种n,n-二乙基-2,4-二氯苯甲脒化合物及其制备方法 |
| ES2660760T3 (es) * | 2013-12-19 | 2018-03-26 | Grünenthal GmbH | Pirrolocarboxamidas fluorometil-sustituidas como bloqueantes del canal de Ca CaV2.2 |
| CA2934327A1 (en) * | 2013-12-19 | 2015-06-25 | Grunenthal Gmbh | Fluoromethyl-substituted pyrrole carboxamides as cav2.2 calcium channel blockers |
| AU2014365740A1 (en) * | 2013-12-19 | 2016-05-26 | Grünenthal GmbH | Fluoromethyl-substituted pyrrole carboxamides iv |
| NL2015814B1 (en) * | 2015-11-19 | 2017-06-06 | Stichting Vu-Vumc | Pyridine-based isocyanides as novel reagents for multicomponent reactions. |
| BR112018012926B1 (pt) | 2015-12-22 | 2022-08-16 | Syngenta Participations Ag | Derivados de pirazol ativos em termos pesticidas, composição pesticida, método para controle de pragas, método para a proteção de material de propagação vegetal do ataque por pragas e material de propagação vegetal revestido |
| CN109897051B (zh) * | 2019-03-31 | 2021-07-09 | 白银乐天园化学有限责任公司 | 一种3-氧杂-8-氮杂-双环[3,2,1]辛烷盐酸盐的制备方法 |
| WO2024036100A1 (en) * | 2022-08-08 | 2024-02-15 | Bristol-Myers Squibb Company | Substituted tetrazolyl compounds useful as t cell activators |
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| US2470084A (en) | 1945-09-25 | 1949-05-17 | Bilhuber Inc E | Substituted alpha-halogen alkyl tetrazoles and process for obtaining the same |
| US5474995A (en) | 1993-06-24 | 1995-12-12 | Merck Frosst Canada, Inc. | Phenyl heterocycles as cox-2 inhibitors |
| US5466823A (en) | 1993-11-30 | 1995-11-14 | G.D. Searle & Co. | Substituted pyrazolyl benzenesulfonamides |
| DE10399017I2 (de) | 1995-02-13 | 2006-04-27 | Searle & Co | Substituierte isoxazole zur behandlung von Entzündung |
| US5633272A (en) | 1995-02-13 | 1997-05-27 | Talley; John J. | Substituted isoxazoles for the treatment of inflammation |
| UA57002C2 (uk) | 1995-10-13 | 2003-06-16 | Мерк Фросст Кенада Енд Ко./Мерк Фросст Кенада Енд Сі. | Похідне (метилсульфоніл)феніл-2-(5н)-фуранону, фармацевтична композиція та спосіб лікування |
| SI22713B (sl) | 1996-04-12 | 2009-12-31 | Searle & Co | Substituirani benzensulfonamidni derivati kot predzdravila COX-2 inhibitorjev |
| SK283261B6 (sk) | 1996-07-18 | 2003-04-01 | Merck Frosst Canada & Co. / Merck Frosst Canada & Cie. | Substituované pyridíny, farmaceutický prostriedok s ich obsahom a ich použitie |
| CO4960662A1 (es) | 1997-08-28 | 2000-09-25 | Novartis Ag | Ciertos acidos 5-alquil-2-arilaminofenilaceticos y sus derivados |
| ATE281458T1 (de) | 1997-09-05 | 2004-11-15 | Glaxo Group Ltd | Pharmazeutische zusammensetzung, enthaltend 2,3- diaryl-pyrazolo(1,5-b)pyridazin derivate |
| TR200101208T2 (tr) | 1998-11-03 | 2001-10-22 | Glaxo Group Limited | Seçici COX-2 inhibitörleri olarak pirazolopiridin türevleri |
| US6025683A (en) | 1998-12-23 | 2000-02-15 | Stryker Corporation | Motor control circuit for regulating a D.C. motor |
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| GB0021494D0 (en) | 2000-09-01 | 2000-10-18 | Glaxo Group Ltd | Chemical comkpounds |
| US7244758B2 (en) * | 2003-05-30 | 2007-07-17 | Neuromed Pharmaceuticals Ltd. | N-type calcium channel blockers |
| CA2534887A1 (en) | 2003-08-08 | 2005-02-24 | Janssen Pharmaceutica, N.V. | Process for the preparation of 2- (quinoxalin-5-ylsulfonylamino) -benzamide compounds |
| US20060211739A1 (en) | 2005-02-08 | 2006-09-21 | Arturo Perez-Medrano | Use of selective P2X7 receptor antagonists |
| PT1928886E (pt) | 2005-09-09 | 2011-07-14 | Glaxosmithkline Llc | Derivados de piridina e sua utilização para o tratamento de distúrbios psicóticos |
| EP1966146B1 (en) | 2005-12-20 | 2011-03-02 | Abbott Healthcare Products B.V. | 4,5-dihydro- (1h)-pyrazole derivatives as cannabinoid cb1 receptor modulators |
| WO2007118323A1 (en) * | 2006-04-17 | 2007-10-25 | Neuromed Pharmaceuticals Ltd. | Isoxazole derivatives as calcium channel blockers |
| AU2008345225A1 (en) | 2007-12-21 | 2009-07-09 | University Of Rochester | Method for altering the lifespan of eukaryotic organisms |
| WO2010034003A2 (en) * | 2008-09-22 | 2010-03-25 | Calcimedica, Inc. | Benzylthiotetrazole inhibitors of store operated calcium release |
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| US20160015687A1 (en) | 2016-01-21 |
| JP2013535414A (ja) | 2013-09-12 |
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| WO2012004604A1 (en) | 2012-01-12 |
| US20130210796A1 (en) | 2013-08-15 |
| US9750719B2 (en) | 2017-09-05 |
| EP2590953A1 (en) | 2013-05-15 |
| ES2529233T3 (es) | 2015-02-18 |
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