JP2008534581A5 - - Google Patents
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- Publication number
- JP2008534581A5 JP2008534581A5 JP2008503954A JP2008503954A JP2008534581A5 JP 2008534581 A5 JP2008534581 A5 JP 2008534581A5 JP 2008503954 A JP2008503954 A JP 2008503954A JP 2008503954 A JP2008503954 A JP 2008503954A JP 2008534581 A5 JP2008534581 A5 JP 2008534581A5
- Authority
- JP
- Japan
- Prior art keywords
- amino
- trifluoromethyl
- dihydropyrido
- oxobutyl
- butyl
- 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.)
- Granted
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- 150000001875 compounds Chemical class 0.000 claims description 19
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 12
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 7
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 claims description 4
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims 45
- 150000003839 salts Chemical class 0.000 claims 39
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 30
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims 30
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims 30
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims 15
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 15
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims 15
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims 15
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims 15
- 239000011976 maleic acid Substances 0.000 claims 15
- 229940098779 methanesulfonic acid Drugs 0.000 claims 15
- 239000011975 tartaric acid Substances 0.000 claims 15
- 235000002906 tartaric acid Nutrition 0.000 claims 15
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims 15
- 229910052736 halogen Inorganic materials 0.000 claims 13
- 150000002367 halogens Chemical class 0.000 claims 13
- 229910052739 hydrogen Inorganic materials 0.000 claims 11
- 239000001257 hydrogen Substances 0.000 claims 11
- -1 3-furan Chemical compound 0.000 claims 9
- 150000002431 hydrogen Chemical class 0.000 claims 8
- 125000001424 substituent group Chemical group 0.000 claims 6
- IKBXXBXFEDIVJH-ZDUSSCGKSA-N 1-[(2s)-2-amino-4-[2-(furan-3-yl)-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-5,5-difluoropiperidin-2-one Chemical compound C([C@@H](N)CC(=O)N1CC2=C(C(=NC(=N2)C2=COC=C2)C(F)(F)F)CC1)N1CC(F)(F)CCC1=O IKBXXBXFEDIVJH-ZDUSSCGKSA-N 0.000 claims 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 4
- 125000001072 heteroaryl group Chemical group 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- 229910052760 oxygen Inorganic materials 0.000 claims 4
- 239000001301 oxygen Substances 0.000 claims 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 3
- VTAQGNVTOHRZRK-NEPJUHHUSA-N (5r)-1-[(2s)-2-amino-4-[2-(fluoromethyl)-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-5-methylpiperidin-2-one Chemical compound C1[C@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(CF)N=C2C(F)(F)F)=C2CC1 VTAQGNVTOHRZRK-NEPJUHHUSA-N 0.000 claims 2
- WALRTZHEUGUMEW-YPMHNXCESA-N (5r)-1-[(2s)-2-amino-4-[2-methyl-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-5-methylpiperidin-2-one Chemical compound C1[C@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(C)N=C2C(F)(F)F)=C2CC1 WALRTZHEUGUMEW-YPMHNXCESA-N 0.000 claims 2
- VDKVOKNVOQJFHM-BBRMVZONSA-N (6s)-4-[(2s)-2-amino-4-[2-(4-fluorophenyl)-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-6-methylmorpholin-2-one Chemical compound C1C(=O)O[C@@H](C)CN1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C=3C=CC(F)=CC=3)=C2CC1 VDKVOKNVOQJFHM-BBRMVZONSA-N 0.000 claims 2
- QXBFXIKTQCKASH-AAEUAGOBSA-N (6s)-4-[(2s)-2-amino-4-[2-cyclopropyl-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-6-methylmorpholin-3-one Chemical compound O=C1CO[C@@H](C)CN1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C3CC3)=C2CC1 QXBFXIKTQCKASH-AAEUAGOBSA-N 0.000 claims 2
- IZJNAQGFGRUTAK-JQWIXIFHSA-N (6s)-4-[(2s)-2-amino-4-[2-methyl-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-6-methylmorpholin-3-one Chemical compound O=C1CO[C@@H](C)CN1C[C@@H](N)CC(=O)N1CC(N=C(C)N=C2C(F)(F)F)=C2CC1 IZJNAQGFGRUTAK-JQWIXIFHSA-N 0.000 claims 2
- PTJKFVGRURDHTO-STQMWFEESA-N (6s)-4-[(2s)-2-amino-4-[2-tert-butyl-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-6-methylmorpholin-3-one Chemical compound O=C1CO[C@@H](C)CN1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C(C)(C)C)=C2CC1 PTJKFVGRURDHTO-STQMWFEESA-N 0.000 claims 2
- WDCJUKKLNWPYDU-JTQLQIEISA-N 1-[(2s)-2-amino-4-[2-(fluoromethyl)-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-5,5-difluoropiperidin-2-one Chemical compound C([C@@H](N)CC(=O)N1CC2=C(C(=NC(CF)=N2)C(F)(F)F)CC1)N1CC(F)(F)CCC1=O WDCJUKKLNWPYDU-JTQLQIEISA-N 0.000 claims 2
- NEVACBBFMZPBCL-NSHDSACASA-N 1-[(2s)-2-amino-4-[2-methyl-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-5,5-difluoropiperidin-2-one Chemical compound C([C@@H](N)CC(=O)N1CC=2N=C(N=C(C=2CC1)C(F)(F)F)C)N1CC(F)(F)CCC1=O NEVACBBFMZPBCL-NSHDSACASA-N 0.000 claims 2
- NRUPLOOESZBVLS-VIFPVBQESA-N 1-[(2s)-2-amino-4-oxo-4-[2-(1,1,2,2,2-pentafluoroethyl)-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]butyl]-5,5-difluoropiperidin-2-one Chemical compound C([C@@H](N)CC(=O)N1CC2=C(C(=NC(=N2)C(F)(F)C(F)(F)F)C(F)(F)F)CC1)N1CC(F)(F)CCC1=O NRUPLOOESZBVLS-VIFPVBQESA-N 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 102000016622 Dipeptidyl Peptidase 4 Human genes 0.000 claims 2
- ZWPRRQZNBDYKLH-VIFPVBQESA-N Gemigliptin Chemical compound C([C@@H](N)CC(=O)N1CC2=C(C(=NC(=N2)C(F)(F)F)C(F)(F)F)CC1)N1CC(F)(F)CCC1=O ZWPRRQZNBDYKLH-VIFPVBQESA-N 0.000 claims 2
- 101000930822 Giardia intestinalis Dipeptidyl-peptidase 4 Proteins 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 239000011593 sulfur Chemical group 0.000 claims 2
- LZXXYWRZDAGXSJ-MNOVXSKESA-N (5r)-1-[(2s)-2-amino-4-[2,4-bis(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-5-methylpiperidin-2-one Chemical compound C1[C@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C(F)(F)F)=C2CC1 LZXXYWRZDAGXSJ-MNOVXSKESA-N 0.000 claims 1
- ZMFRTOJDRJYDQC-KGLIPLIRSA-N (5r)-1-[(2s)-2-amino-4-[2-(2-methoxyethyl)-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-5-methylpiperidin-2-one Chemical compound C([C@@H](N)CC(=O)N1CC=2N=C(N=C(C=2CC1)C(F)(F)F)CCOC)N1C[C@H](C)CCC1=O ZMFRTOJDRJYDQC-KGLIPLIRSA-N 0.000 claims 1
- GJAGXFGOQJDHMG-HIFRSBDPSA-N (5r)-1-[(2s)-2-amino-4-[2-(3,4-difluorophenyl)-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-5-methylpiperidin-2-one Chemical compound C1[C@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C=3C=C(F)C(F)=CC=3)=C2CC1 GJAGXFGOQJDHMG-HIFRSBDPSA-N 0.000 claims 1
- YTHMPIPXDYQIFH-PBHICJAKSA-N (5r)-1-[(2s)-2-amino-4-[2-(4-fluorophenyl)-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-5-methylpiperidin-2-one Chemical compound C1[C@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C=3C=CC(F)=CC=3)=C2CC1 YTHMPIPXDYQIFH-PBHICJAKSA-N 0.000 claims 1
- BBQAKAGYXGKXMJ-PBHICJAKSA-N (5r)-1-[(2s)-2-amino-4-[2-(4-fluorophenyl)-6,7-dihydro-4h-[1,3]thiazolo[4,5-c]pyridin-5-yl]-4-oxobutyl]-5-methylpiperidin-2-one Chemical compound C1[C@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(S2)C=3C=CC(F)=CC=3)=C2CC1 BBQAKAGYXGKXMJ-PBHICJAKSA-N 0.000 claims 1
- HOZVRGBYSDXNDD-HIFRSBDPSA-N (5r)-1-[(2s)-2-amino-4-[2-(cyclopropylmethyl)-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-5-methylpiperidin-2-one Chemical compound C1[C@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(CC2CC2)N=C2C(F)(F)F)=C2CC1 HOZVRGBYSDXNDD-HIFRSBDPSA-N 0.000 claims 1
- GYATXFQPZVGGMJ-KGLIPLIRSA-N (5r)-1-[(2s)-2-amino-4-[2-(furan-2-yl)-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-5-methylpiperidin-2-one Chemical compound C1[C@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C=3OC=CC=3)=C2CC1 GYATXFQPZVGGMJ-KGLIPLIRSA-N 0.000 claims 1
- GHNBAWWYZOLGQW-HIFRSBDPSA-N (5r)-1-[(2s)-2-amino-4-[2-(furan-3-yl)-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-5-methylpiperidin-2-one Chemical compound C1[C@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C3=COC=C3)=C2CC1 GHNBAWWYZOLGQW-HIFRSBDPSA-N 0.000 claims 1
- NICJDAWRKKKROW-QAPCUYQASA-N (5r)-1-[(2s)-2-amino-4-[2-[(4-fluorophenyl)methyl]-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-5-methylpiperidin-2-one Chemical compound C1[C@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(CC=2C=CC(F)=CC=2)N=C2C(F)(F)F)=C2CC1 NICJDAWRKKKROW-QAPCUYQASA-N 0.000 claims 1
- ZLQXPIQSMPTOGU-HIFRSBDPSA-N (5r)-1-[(2s)-2-amino-4-[2-cyclobutyl-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-5-methylpiperidin-2-one Chemical compound C1[C@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C3CCC3)=C2CC1 ZLQXPIQSMPTOGU-HIFRSBDPSA-N 0.000 claims 1
- DJNMQSVECLAYMK-ZBFHGGJFSA-N (5r)-1-[(2s)-2-amino-4-[2-cyclopentyl-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-5-methylpiperidin-2-one Chemical compound C1[C@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C3CCCC3)=C2CC1 DJNMQSVECLAYMK-ZBFHGGJFSA-N 0.000 claims 1
- XIGSSFWYVCBXNQ-MNOVXSKESA-N (5r)-1-[(2s)-2-amino-4-oxo-4-[2-(1,1,2,2,2-pentafluoroethyl)-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]butyl]-5-methylpiperidin-2-one Chemical compound C1[C@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C(F)(F)C(F)(F)F)=C2CC1 XIGSSFWYVCBXNQ-MNOVXSKESA-N 0.000 claims 1
- XZJSGVSUEMLGAD-PBHICJAKSA-N (5r)-1-[(2s)-2-amino-4-oxo-4-[2-[4-(trifluoromethyl)phenyl]-6,7-dihydro-4h-[1,3]thiazolo[4,5-c]pyridin-5-yl]butyl]-5-methylpiperidin-2-one Chemical compound C1[C@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(S2)C=3C=CC(=CC=3)C(F)(F)F)=C2CC1 XZJSGVSUEMLGAD-PBHICJAKSA-N 0.000 claims 1
- KOARBUHQPKZLHB-WBVHZDCISA-N (5r)-1-[(2s)-2-amino-4-oxo-4-[2-phenyl-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]butyl]-5-methylpiperidin-2-one Chemical compound C1[C@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C=3C=CC=CC=3)=C2CC1 KOARBUHQPKZLHB-WBVHZDCISA-N 0.000 claims 1
- PTZUFFHRUUTPSB-KGLIPLIRSA-N (5r)-1-[(2s)-2-amino-4-oxo-4-[2-propyl-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]butyl]-5-methylpiperidin-2-one Chemical compound C([C@@H](N)CC(=O)N1CC=2N=C(N=C(C=2CC1)C(F)(F)F)CCC)N1C[C@H](C)CCC1=O PTZUFFHRUUTPSB-KGLIPLIRSA-N 0.000 claims 1
- DIMNCOWKJPBZTI-ZBFHGGJFSA-N (5r)-1-[(2s)-2-amino-4-oxo-4-[2-pyridin-3-yl-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]butyl]-5-methylpiperidin-2-one Chemical compound C1[C@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C=3C=NC=CC=3)=C2CC1 DIMNCOWKJPBZTI-ZBFHGGJFSA-N 0.000 claims 1
- RNXARZUJEQCSDC-ZBFHGGJFSA-N (5r)-1-[(2s)-2-amino-4-oxo-4-[2-pyridin-4-yl-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]butyl]-5-methylpiperidin-2-one Chemical compound C1[C@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C=3C=CN=CC=3)=C2CC1 RNXARZUJEQCSDC-ZBFHGGJFSA-N 0.000 claims 1
- HVKRQGSOVNNKQT-KGLIPLIRSA-N (5r)-1-[(2s)-2-amino-4-oxo-4-[2-thiophen-2-yl-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]butyl]-5-methylpiperidin-2-one Chemical compound C1[C@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C=3SC=CC=3)=C2CC1 HVKRQGSOVNNKQT-KGLIPLIRSA-N 0.000 claims 1
- QTXOAUMQCVDJGC-HIFRSBDPSA-N (5r)-1-[(2s)-2-amino-4-oxo-4-[2-thiophen-3-yl-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]butyl]-5-methylpiperidin-2-one Chemical compound C1[C@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C3=CSC=C3)=C2CC1 QTXOAUMQCVDJGC-HIFRSBDPSA-N 0.000 claims 1
- LZXXYWRZDAGXSJ-QWRGUYRKSA-N (5s)-1-[(2s)-2-amino-4-[2,4-bis(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-5-methylpiperidin-2-one Chemical compound C1[C@@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C(F)(F)F)=C2CC1 LZXXYWRZDAGXSJ-QWRGUYRKSA-N 0.000 claims 1
- PNJOUWGUDCMGPW-QWRGUYRKSA-N (5s)-1-[(2s)-2-amino-4-oxo-4-[3-(trifluoromethyl)-6,8-dihydro-5h-[1,2,4]triazolo[4,3-a]pyrazin-7-yl]butyl]-5-methylpiperidin-2-one Chemical compound C1[C@@H](C)CCC(=O)N1C[C@@H](N)CC(=O)N1CC2=NN=C(C(F)(F)F)N2CC1 PNJOUWGUDCMGPW-QWRGUYRKSA-N 0.000 claims 1
- DASWVISTCFTOIS-ZJUUUORDSA-N (6r)-4-[(2s)-2-amino-4-oxo-4-[3-(trifluoromethyl)-6,8-dihydro-5h-[1,2,4]triazolo[4,3-a]pyrazin-7-yl]butyl]-6-methylmorpholin-3-one Chemical compound O=C1CO[C@H](C)CN1C[C@@H](N)CC(=O)N1CC2=NN=C(C(F)(F)F)N2CC1 DASWVISTCFTOIS-ZJUUUORDSA-N 0.000 claims 1
- QYTRYTQNQKXPRC-JSGCOSHPSA-N (6s)-4-[(2s)-2-amino-4-[2-(3,4-difluorophenyl)-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-6-methylmorpholin-3-one Chemical compound O=C1CO[C@@H](C)CN1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C=3C=C(F)C(F)=CC=3)=C2CC1 QYTRYTQNQKXPRC-JSGCOSHPSA-N 0.000 claims 1
- UOBNYVYEPQSIGK-BBRMVZONSA-N (6s)-4-[(2s)-2-amino-4-[2-(3-fluorophenyl)-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-6-methylmorpholin-3-one Chemical compound O=C1CO[C@@H](C)CN1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C=3C=C(F)C=CC=3)=C2CC1 UOBNYVYEPQSIGK-BBRMVZONSA-N 0.000 claims 1
- GZNNXRIBKPNKJU-BBRMVZONSA-N (6s)-4-[(2s)-2-amino-4-[2-(4-fluorophenyl)-6,7-dihydro-4h-[1,3]thiazolo[4,5-c]pyridin-5-yl]-4-oxobutyl]-6-methylmorpholin-3-one Chemical compound O=C1CO[C@@H](C)CN1C[C@@H](N)CC(=O)N1CC(N=C(S2)C=3C=CC(F)=CC=3)=C2CC1 GZNNXRIBKPNKJU-BBRMVZONSA-N 0.000 claims 1
- XALIVERBROSNTF-ZFWWWQNUSA-N (6s)-4-[(2s)-2-amino-4-[2-cyclopentyl-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-6-methylmorpholin-3-one Chemical compound O=C1CO[C@@H](C)CN1C[C@@H](N)CC(=O)N1CC(N=C(N=C2C(F)(F)F)C3CCCC3)=C2CC1 XALIVERBROSNTF-ZFWWWQNUSA-N 0.000 claims 1
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- XVYVGRBMSDRCMF-NSHDSACASA-N 1-[(2s)-2-amino-4-[2-ethyl-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]-4-oxobutyl]-5,5-difluoropiperidin-2-one Chemical compound C([C@@H](N)CC(=O)N1CC=2N=C(N=C(C=2CC1)C(F)(F)F)CC)N1CC(F)(F)CCC1=O XVYVGRBMSDRCMF-NSHDSACASA-N 0.000 claims 1
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- AGEBFSDHNBLHRV-KZUDCZAMSA-N 1-[(2s)-2-amino-4-oxo-4-[2-propan-2-yl-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]butyl]-5-methylpiperidin-2-one Chemical compound C([C@@H](N)CC(=O)N1CC=2N=C(N=C(C=2CC1)C(F)(F)F)C(C)C)N1CC(C)CCC1=O AGEBFSDHNBLHRV-KZUDCZAMSA-N 0.000 claims 1
- BURQKBQMSLDOEB-LBPRGKRZSA-N 1-[(2s)-2-amino-4-oxo-4-[2-propyl-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]butyl]-5,5-difluoropiperidin-2-one Chemical compound C([C@@H](N)CC(=O)N1CC=2N=C(N=C(C=2CC1)C(F)(F)F)CCC)N1CC(F)(F)CCC1=O BURQKBQMSLDOEB-LBPRGKRZSA-N 0.000 claims 1
- ASNFYBPTMBOSDI-AWEZNQCLSA-N 1-[(2s)-2-amino-4-oxo-4-[2-pyridin-4-yl-4-(trifluoromethyl)-6,8-dihydro-5h-pyrido[3,4-d]pyrimidin-7-yl]butyl]-5,5-difluoropiperidin-2-one Chemical compound C([C@@H](N)CC(=O)N1CC2=C(C(=NC(=N2)C=2C=CN=CC=2)C(F)(F)F)CC1)N1CC(F)(F)CCC1=O ASNFYBPTMBOSDI-AWEZNQCLSA-N 0.000 claims 1
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Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007148185A2 (en) | 2006-06-21 | 2007-12-27 | Pfizer Products Inc. | Substituted 3 -amino- pyrrolidino-4 -lactams as dpp inhibitors |
| AU2007283113A1 (en) | 2006-08-08 | 2008-02-14 | Sanofi-Aventis | Arylaminoaryl-alkyl-substituted imidazolidine-2,4-diones, processes for preparing them, medicaments comprising these compounds, and their use |
| KR20120030570A (ko) | 2007-04-03 | 2012-03-28 | 미쓰비시 타나베 파마 코퍼레이션 | 디펩티딜 펩티다아제 4 저해 화합물과 감미료와의 병용 |
| CN101357922B (zh) * | 2007-08-02 | 2011-05-18 | 山东轩竹医药科技有限公司 | 新的dpp-iv抑制剂 |
| EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| AU2008333110A1 (en) * | 2007-12-05 | 2009-06-11 | Astrazeneca Ab (Publ) | New compounds III |
| AU2008341352B2 (en) * | 2007-12-21 | 2013-08-01 | Lg Chem, Ltd. | Dipeptidyl peptidase-IV inhibiting compounds, methods of preparing the same, and pharmaceutical compositions containing the same as active agent |
| CL2008003653A1 (es) | 2008-01-17 | 2010-03-05 | Mitsubishi Tanabe Pharma Corp | Uso de un inhibidor de sglt derivado de glucopiranosilo y un inhibidor de dppiv seleccionado para tratar la diabetes; y composicion farmaceutica. |
| CN101486689B (zh) * | 2008-01-18 | 2011-08-10 | 山东轩竹医药科技有限公司 | 具有磺酰胺基甲酰胺哌嗪结构的dpp-iv抑制剂 |
| UY31968A (es) | 2008-07-09 | 2010-01-29 | Sanofi Aventis | Nuevos derivados heterocíclicos, sus procesos para su preparación, y sus usos terapéuticos |
| JO2870B1 (en) * | 2008-11-13 | 2015-03-15 | ميرك شارب اند دوهم كورب | Amino Tetra Hydro Pirans as Inhibitors of Peptide Dipeptide IV for the Treatment or Prevention of Diabetes |
| WO2010068601A1 (en) | 2008-12-08 | 2010-06-17 | Sanofi-Aventis | A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof |
| CA2754712A1 (en) * | 2009-03-13 | 2010-09-16 | Sun Chemical B.V. | Cyclic carbamate compounds useful in energy-curable compositions |
| BR112012003973A2 (pt) | 2009-08-26 | 2015-09-08 | Sanofi Sa | hidratos de fluoroglicosídeo heteroaromático cristalinos, produtos farmacêuticos compreendendo estes compostos e seu uso |
| US8871760B2 (en) * | 2009-09-21 | 2014-10-28 | Roche Palo Alto Llc | [1,2,4]triazolo[3,4-C][1,4]oxazines as P2X7 modulators |
| WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| CN102260265B (zh) * | 2010-05-24 | 2015-09-02 | 上海阳帆医药科技有限公司 | 六氢吡咯[3,4-b]吡咯衍生物、其制备方法及其用途 |
| US8933024B2 (en) | 2010-06-18 | 2015-01-13 | Sanofi | Azolopyridin-3-one derivatives as inhibitors of lipases and phospholipases |
| US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| EA022500B1 (ru) | 2010-09-03 | 2016-01-29 | Эл Джи Лайф Сайенсиз Лтд. | Способ получения промежуточного соединения для синтеза лекарственного средства |
| TWI519533B (zh) * | 2010-11-01 | 2016-02-01 | Ｌｇ生命科學有限公司 | １－｛（２Ｓ）－２－胺基－４－［２，４－雙（三氟甲基）－５，８－二氫吡啶并［３，４－ｄ］嘧啶－７（６Ｈ）－基］－４－側氧丁基｝－５，５－二氟哌啶－２－酮酒石酸鹽之水合物 |
| WO2012120052A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
| WO2012120056A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Tetrasubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| US8710050B2 (en) | 2011-03-08 | 2014-04-29 | Sanofi | Di and tri- substituted oxathiazine derivatives, method for the production, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| WO2012120053A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Verzweigte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| EP2683705B1 (de) | 2011-03-08 | 2015-04-22 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| WO2012170702A1 (en) | 2011-06-08 | 2012-12-13 | Arena Pharmaceuticals, Inc. | Modulators of the gpr119 receptor and the treatment of disorders related thereto |
| WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| WO2013045413A1 (en) | 2011-09-27 | 2013-04-04 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| WO2014064215A1 (en) | 2012-10-24 | 2014-05-01 | INSERM (Institut National de la Santé et de la Recherche Médicale) | TPL2 KINASE INHIBITORS FOR PREVENTING OR TREATING DIABETES AND FOR PROMOTING β-CELL SURVIVAL |
| CN105085528A (zh) * | 2014-05-15 | 2015-11-25 | 成都贝斯凯瑞生物科技有限公司 | 作为二肽基肽酶-iv抑制剂的氨基四氢吡喃衍生物 |
| EP3273981B1 (en) | 2015-03-24 | 2020-04-29 | INSERM - Institut National de la Santé et de la Recherche Médicale | Method and pharmaceutical composition for use in the treatment of diabetes |
| WO2017147312A1 (en) | 2016-02-23 | 2017-08-31 | Indiana University Research & Technology Corporation | Combination therapies for treatment of spinal muscular atrophy |
| KR102068754B1 (ko) * | 2017-04-20 | 2020-01-21 | 주식회사 엘지화학 | 의약품 합성용 중간체 화합물의 제조 방법 |
| KR102184129B1 (ko) * | 2017-11-16 | 2020-11-27 | 주식회사 엘지화학 | 의약품 합성용 중간체 화합물의 제조 방법 |
| CN108191647B (zh) * | 2018-02-22 | 2020-09-29 | 江苏尚莱特医药化工材料有限公司 | 2,2-二氟二羧酸二烷基酯的合成方法 |
| CN111537622B (zh) * | 2019-11-29 | 2021-11-26 | 杭州华东医药集团新药研究院有限公司 | 一种度格列汀及其盐的杂质的检测方法 |
| KR20250097733A (ko) | 2023-12-21 | 2025-06-30 | 이니스트에스티 주식회사 | 디펩티딜 펩티데이즈-iv (dpp-iv) 억제제의 신규한 염, 이의 제조 방법 및 이를 포함하는 약제학적 조성물 |
| KR20250137744A (ko) | 2024-03-11 | 2025-09-19 | 엠에프씨 주식회사 | 제미글립틴의 신규 결정형 및 이의 제조방법 |
| KR20250147756A (ko) | 2024-03-27 | 2025-10-14 | 엠에프씨 주식회사 | 신규한 형태의 제미글립틴 말산염 결정형 및 이의 제조방법 |
| KR20250155700A (ko) | 2024-04-24 | 2025-10-31 | 주식회사 다산제약 | 제미글립틴 산부가염 제조방법 및 이를 유효성분으로 포함하는 dpp-4 저해용 조성물 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CO5150173A1 (es) | 1998-12-10 | 2002-04-29 | Novartis Ag | Compuestos n-(glicilo sustituido)-2-cianopirrolidinas inhibidores de peptidasa de dipeptidilo-iv (dpp-iv) los cuales son efectivos en el tratamiento de condiciones mediadas por la inhibicion de dpp-iv |
| UA74912C2 (en) | 2001-07-06 | 2006-02-15 | Merck & Co Inc | Beta-aminotetrahydroimidazo-(1,2-a)-pyrazines and tetratriazolo-(4,3-a)-pyrazines as inhibitors of dipeptylpeptidase for the treatment or prevention of diabetes |
| US6861440B2 (en) * | 2001-10-26 | 2005-03-01 | Hoffmann-La Roche Inc. | DPP IV inhibitors |
| WO2003057144A2 (en) * | 2001-12-26 | 2003-07-17 | Guilford Pharmaceuticals | Change inhibitors of dipeptidyl peptidase iv |
| US7307164B2 (en) * | 2002-03-25 | 2007-12-11 | Merck & Co., Inc. | β-amino heterocyclic dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| CA2483843A1 (en) * | 2002-04-29 | 2003-11-13 | Merck & Co. Inc. | Tetrahydropyranyl cyclopentyl tetrahydroisoquinoline modulators of chemokine receptor activity |
| JP4530852B2 (ja) * | 2002-07-15 | 2010-08-25 | メルク・シャープ・エンド・ドーム・コーポレイション | 糖尿病治療のためのピペリジノピリミジンジペプチジルペプチダーゼ阻害剤 |
| JP2004285325A (ja) * | 2002-12-17 | 2004-10-14 | Fuji Photo Film Co Ltd | パターン形成方法及び物質付着パターン材料 |
| CA2508947A1 (en) * | 2002-12-20 | 2004-07-15 | Merck & Co., Inc. | 3-amino-4-phenylbutanoic acid derivatives as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| US7265128B2 (en) * | 2003-01-17 | 2007-09-04 | Merck & Co., Inc. | 3-amino-4-phenylbutanoic acid derivatives as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| CA2513684A1 (en) | 2003-01-31 | 2004-08-19 | Merck & Co., Inc. | 3-amino-4-phenylbutanoic acid derivatives as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| EP1732885A1 (en) * | 2004-02-23 | 2006-12-20 | Trustees Of Tufts College | Lactams as conformationally constrained peptidomimetic inhibitors |
| US7291427B2 (en) * | 2004-03-19 | 2007-11-06 | Fujifilm Corporation | Surface graft material, conductive pattern material, and production method thereof |
| DE102004020908A1 (de) * | 2004-04-28 | 2005-11-17 | Grünenthal GmbH | Substituierte 5,6,7,8,-Tetrahydro-pyrido[4,3-d]pyrimidin-2-yl- und 5,6,7,8,-Tetrahydro-chinazolin-2-yl-Verbindungen |
| DE102005016170A1 (de) * | 2005-04-07 | 2006-10-12 | Grünenthal GmbH | 4,5,6,7- Tetrahydro-isoxazolo(4,5c)pyridin-Verbindungen und deren Verwendung zur Herstellung von Arzneimitteln |
| ZA200709961B (en) * | 2005-05-10 | 2009-07-29 | Vertex Pharma | Bicyclic derivatives as modulators of ion channels |
| JP2009537558A (ja) * | 2006-05-16 | 2009-10-29 | スミスクライン・ビーチャム・コーポレイション | プロリルヒドロキシラーゼ阻害剤 |
| EP2229395A1 (en) * | 2008-01-17 | 2010-09-22 | Grünenthal GmbH | Substituted sulfonamide derivatives |
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