KR20120105449A - 오렉신 수용체 조절제로서의 이치환된 옥타하이드로피롤로[3,4-c]피롤 - Google Patents
오렉신 수용체 조절제로서의 이치환된 옥타하이드로피롤로[3,4-c]피롤 Download PDFInfo
- Publication number
- KR20120105449A KR20120105449A KR1020127013101A KR20127013101A KR20120105449A KR 20120105449 A KR20120105449 A KR 20120105449A KR 1020127013101 A KR1020127013101 A KR 1020127013101A KR 20127013101 A KR20127013101 A KR 20127013101A KR 20120105449 A KR20120105449 A KR 20120105449A
- Authority
- KR
- South Korea
- Prior art keywords
- pyrrole
- phenyl
- triazol
- carbonyl
- fluoro
- 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.)
- Withdrawn
Links
- 0 *N1CC(CNC2)C2C1 Chemical compound *N1CC(CNC2)C2C1 0.000 description 6
- AOBSJQWEYXEPBK-UHFFFAOYSA-N C(c1ccccc1)N1CC(CNC2)C2C1 Chemical compound C(c1ccccc1)N1CC(CNC2)C2C1 AOBSJQWEYXEPBK-UHFFFAOYSA-N 0.000 description 3
- YSBZBSOUZKHASD-UHFFFAOYSA-N C1NCC(C2)C1CN2c1nccc(-c2ccccc2)n1 Chemical compound C1NCC(C2)C1CN2c1nccc(-c2ccccc2)n1 YSBZBSOUZKHASD-UHFFFAOYSA-N 0.000 description 1
- FYUVLZRRIRGSTE-UHFFFAOYSA-N CC(C)(C)OC(N1CC(CNC2)C2C1)=O Chemical compound CC(C)(C)OC(N1CC(CNC2)C2C1)=O FYUVLZRRIRGSTE-UHFFFAOYSA-N 0.000 description 1
- MIUDTRFMDYMLHR-UHFFFAOYSA-N CC(C)(C)c(cc1C(N(C2)CC(C3)C2CN3c2nc(C)cc(C)n2)=O)ccc1OC Chemical compound CC(C)(C)c(cc1C(N(C2)CC(C3)C2CN3c2nc(C)cc(C)n2)=O)ccc1OC MIUDTRFMDYMLHR-UHFFFAOYSA-N 0.000 description 1
- ICKRORFDNACZKJ-UHFFFAOYSA-N CC1(C)C=C(C(N(C2)CC(C3)C2CN3c2nc(C)cnc2)=O)C([n]2nccn2)=CC1 Chemical compound CC1(C)C=C(C(N(C2)CC(C3)C2CN3c2nc(C)cnc2)=O)C([n]2nccn2)=CC1 ICKRORFDNACZKJ-UHFFFAOYSA-N 0.000 description 1
- GZPFTNSJBAEJET-UHFFFAOYSA-N CCCOc1cccnc1C(N(C1)CC(C2)C1CN2c1nc(cccc2)c2nc1)=O Chemical compound CCCOc1cccnc1C(N(C1)CC(C2)C1CN2c1nc(cccc2)c2nc1)=O GZPFTNSJBAEJET-UHFFFAOYSA-N 0.000 description 1
- JCZKDUWJCWYWSC-UHFFFAOYSA-N CN(C)c1nc(OC)cc(N2CC(CN(C3)C(c(cccc4)c4-[n]4nccn4)=O)C3C2)n1 Chemical compound CN(C)c1nc(OC)cc(N2CC(CN(C3)C(c(cccc4)c4-[n]4nccn4)=O)C3C2)n1 JCZKDUWJCWYWSC-UHFFFAOYSA-N 0.000 description 1
- NFCRLAPCIIYXMT-UHFFFAOYSA-N COc(cc1)cc(OC)c1C(N1CC(CNC2)C2C1)=O Chemical compound COc(cc1)cc(OC)c1C(N1CC(CNC2)C2C1)=O NFCRLAPCIIYXMT-UHFFFAOYSA-N 0.000 description 1
- OFURCFFCWJMVKQ-UHFFFAOYSA-N COc(cc1C(O)=O)ccc1-[n]1nccn1 Chemical compound COc(cc1C(O)=O)ccc1-[n]1nccn1 OFURCFFCWJMVKQ-UHFFFAOYSA-N 0.000 description 1
- CEEJDSMUCVNQJG-UHFFFAOYSA-N COc1ccccc1S(N1CC(CN(C2)c3ncc(C(F)(F)F)cc3)C2C1)(=O)=O Chemical compound COc1ccccc1S(N1CC(CN(C2)c3ncc(C(F)(F)F)cc3)C2C1)(=O)=O CEEJDSMUCVNQJG-UHFFFAOYSA-N 0.000 description 1
- OGHLIVQBOUOCAF-UHFFFAOYSA-N COc1ccnc(N2CC(CN(C3)C(c(cccc4)c4-c4cccc(F)c4)=O)C3C2)n1 Chemical compound COc1ccnc(N2CC(CN(C3)C(c(cccc4)c4-c4cccc(F)c4)=O)C3C2)n1 OGHLIVQBOUOCAF-UHFFFAOYSA-N 0.000 description 1
- VANHUDWGAHAKBW-UHFFFAOYSA-N COc1ccnc(N2CC(CN(C3)C(c4cc(F)ccc4-c4ncccn4)=O)C3C2)n1 Chemical compound COc1ccnc(N2CC(CN(C3)C(c4cc(F)ccc4-c4ncccn4)=O)C3C2)n1 VANHUDWGAHAKBW-UHFFFAOYSA-N 0.000 description 1
- DBQFXQNGQUPVER-UHFFFAOYSA-N Cc(c(C)n1)cnc1Cl Chemical compound Cc(c(C)n1)cnc1Cl DBQFXQNGQUPVER-UHFFFAOYSA-N 0.000 description 1
- PBILPYOXHBBIOB-UHFFFAOYSA-N Cc(nc(N1CC(CN(C2)C(C(CCC=C3)=C3[n]3nccn3)=O)C2C1)nc1)c1F Chemical compound Cc(nc(N1CC(CN(C2)C(C(CCC=C3)=C3[n]3nccn3)=O)C2C1)nc1)c1F PBILPYOXHBBIOB-UHFFFAOYSA-N 0.000 description 1
- OIIUFHFKINSBPW-UHFFFAOYSA-N Cc(nc(N1CC(CN(C2)C(c3ccccc3-c3n[n](C)cn3)=O)C2C1)nc1)c1F Chemical compound Cc(nc(N1CC(CN(C2)C(c3ccccc3-c3n[n](C)cn3)=O)C2C1)nc1)c1F OIIUFHFKINSBPW-UHFFFAOYSA-N 0.000 description 1
- KAKQLZPCIDXJDG-UHFFFAOYSA-N Cc1c(C(N(C2)CC(C3)C2CN3c2nc(C)cc(C)n2)=O)[o]cc1 Chemical compound Cc1c(C(N(C2)CC(C3)C2CN3c2nc(C)cc(C)n2)=O)[o]cc1 KAKQLZPCIDXJDG-UHFFFAOYSA-N 0.000 description 1
- GZCZWBDVPLUTNE-UHFFFAOYSA-N Cc1c(C)nc(N2CC(CN(C3)C(c4c(-c5ccn[nH]5)nccc4)=O)C3C2)nc1C Chemical compound Cc1c(C)nc(N2CC(CN(C3)C(c4c(-c5ccn[nH]5)nccc4)=O)C3C2)nc1C GZCZWBDVPLUTNE-UHFFFAOYSA-N 0.000 description 1
- BVINMOXFXQBPAM-UHFFFAOYSA-N Cc1cc(C)nc(N2CC(CN(C3)C(c([s]cc4)c4-c4ccccc4)=O)C3C2)n1 Chemical compound Cc1cc(C)nc(N2CC(CN(C3)C(c([s]cc4)c4-c4ccccc4)=O)C3C2)n1 BVINMOXFXQBPAM-UHFFFAOYSA-N 0.000 description 1
- KYQDZVMSJLXAST-UHFFFAOYSA-N Cc1cc(C)nc(N2CC(CN(C3)C(c(c(F)ccc4)c4F)=O)C3C2)n1 Chemical compound Cc1cc(C)nc(N2CC(CN(C3)C(c(c(F)ccc4)c4F)=O)C3C2)n1 KYQDZVMSJLXAST-UHFFFAOYSA-N 0.000 description 1
- UEVARSJJPMCNMC-UHFFFAOYSA-N Cc1cc(C)nc(N2CC(CN(C3)C(c(ccc4c5cccc4)c5OC)=O)C3C2)n1 Chemical compound Cc1cc(C)nc(N2CC(CN(C3)C(c(ccc4c5cccc4)c5OC)=O)C3C2)n1 UEVARSJJPMCNMC-UHFFFAOYSA-N 0.000 description 1
- SJLACDBRLFYAGQ-UHFFFAOYSA-N Cc1cc(C)nc(N2CC(CN(C3)C(c(cccc4)c4-c4cc(F)ccc4)=O)C3C2)n1 Chemical compound Cc1cc(C)nc(N2CC(CN(C3)C(c(cccc4)c4-c4cc(F)ccc4)=O)C3C2)n1 SJLACDBRLFYAGQ-UHFFFAOYSA-N 0.000 description 1
- HUWGVGRNCHMZBQ-UHFFFAOYSA-N Cc1cc(O)nc(N2CC(CN(C3)C(c(c(F)ccc4)c4-[n]4nccn4)=O)C3C2)n1 Chemical compound Cc1cc(O)nc(N2CC(CN(C3)C(c(c(F)ccc4)c4-[n]4nccn4)=O)C3C2)n1 HUWGVGRNCHMZBQ-UHFFFAOYSA-N 0.000 description 1
- QKLAYBSWOAYZAN-UHFFFAOYSA-N Cc1ccnc(N2CC(CN(C3)C(c(cccc4)c4-[n]4nccn4)=O)C3C2)n1 Chemical compound Cc1ccnc(N2CC(CN(C3)C(c(cccc4)c4-[n]4nccn4)=O)C3C2)n1 QKLAYBSWOAYZAN-UHFFFAOYSA-N 0.000 description 1
- AJFJWKCDKOIHQS-UHFFFAOYSA-N Cc1ccnc(N2CC(CN(C3)C(c(cccc4)c4-c4ccc[s]4)=O)C3C2)n1 Chemical compound Cc1ccnc(N2CC(CN(C3)C(c(cccc4)c4-c4ccc[s]4)=O)C3C2)n1 AJFJWKCDKOIHQS-UHFFFAOYSA-N 0.000 description 1
- CACDHKJTVIUGEW-UHFFFAOYSA-N Cc1nc(C(N2CC(CNC3)C3C2)=O)c(-c(cc2)ccc2F)[s]1 Chemical compound Cc1nc(C(N2CC(CNC3)C3C2)=O)c(-c(cc2)ccc2F)[s]1 CACDHKJTVIUGEW-UHFFFAOYSA-N 0.000 description 1
- OAMKHVKQSSRCDJ-UHFFFAOYSA-N Cc1nc(N2CC(CN(C3)C(c4cc(F)ccc4-[n]4nccn4)=O)C3C2)nc(N(C)C)c1 Chemical compound Cc1nc(N2CC(CN(C3)C(c4cc(F)ccc4-[n]4nccn4)=O)C3C2)nc(N(C)C)c1 OAMKHVKQSSRCDJ-UHFFFAOYSA-N 0.000 description 1
- IBTOYHUCRVSPJX-UHFFFAOYSA-N Cc1nc(N2CC(CN(C3)C(c4ccccc4-c4ccccn4)=O)C3C2)nc(C)c1 Chemical compound Cc1nc(N2CC(CN(C3)C(c4ccccc4-c4ccccn4)=O)C3C2)nc(C)c1 IBTOYHUCRVSPJX-UHFFFAOYSA-N 0.000 description 1
- XBDFZGUATPAMHJ-UHFFFAOYSA-N FC(c1nc(N2CC(CNC3)C3C2)ncc1)(F)F Chemical compound FC(c1nc(N2CC(CNC3)C3C2)ncc1)(F)F XBDFZGUATPAMHJ-UHFFFAOYSA-N 0.000 description 1
- DQNFPCOVVBRXOY-UHFFFAOYSA-N Nc(cccc1C(O2)=O)c1C2=O Chemical compound Nc(cccc1C(O2)=O)c1C2=O DQNFPCOVVBRXOY-UHFFFAOYSA-N 0.000 description 1
- MGBKJKDRMRAZKC-UHFFFAOYSA-N Nc(cccc1O)c1O Chemical compound Nc(cccc1O)c1O MGBKJKDRMRAZKC-UHFFFAOYSA-N 0.000 description 1
- PBCULYFYQCLGFO-UHFFFAOYSA-N O=C(c(cccc1)c1-[n]1nccn1)N(C1)CC(C2)C1CN2c1nc(cccc2)c2nc1 Chemical compound O=C(c(cccc1)c1-[n]1nccn1)N(C1)CC(C2)C1CN2c1nc(cccc2)c2nc1 PBCULYFYQCLGFO-UHFFFAOYSA-N 0.000 description 1
- MIEKLHFLBFABFC-UHFFFAOYSA-N O=C(c(cccc1)c1-c1ccc[s]1)N(C1)CC(C2)C1CN2c1nccc(-c2c[nH]nc2)n1 Chemical compound O=C(c(cccc1)c1-c1ccc[s]1)N(C1)CC(C2)C1CN2c1nccc(-c2c[nH]nc2)n1 MIEKLHFLBFABFC-UHFFFAOYSA-N 0.000 description 1
- LFMLAHRDGHNRMB-UHFFFAOYSA-N O=C(c1ccccc1-c1ccc[s]1)N(C1)CC(C2)C1CN2c1nc(C(F)(F)F)ccc1 Chemical compound O=C(c1ccccc1-c1ccc[s]1)N(C1)CC(C2)C1CN2c1nc(C(F)(F)F)ccc1 LFMLAHRDGHNRMB-UHFFFAOYSA-N 0.000 description 1
- XCFOXTRGQAEXQS-UHFFFAOYSA-N O=C(c1ccccc1-c1ccccc1)N(C1)CC(C2)C1CN2c1nc(cccc2)c2nc1 Chemical compound O=C(c1ccccc1-c1ccccc1)N(C1)CC(C2)C1CN2c1nc(cccc2)c2nc1 XCFOXTRGQAEXQS-UHFFFAOYSA-N 0.000 description 1
- ANLUMVSLJBEEDV-UHFFFAOYSA-N O=S(c(cccc1)c1-c1ccccc1)(N1CC(CN(C2)c3nc(cccc4)c4nc3)C2C1)=O Chemical compound O=S(c(cccc1)c1-c1ccccc1)(N1CC(CN(C2)c3nc(cccc4)c4nc3)C2C1)=O ANLUMVSLJBEEDV-UHFFFAOYSA-N 0.000 description 1
- GWFSRJKDYXADOG-UHFFFAOYSA-N OC(c(cc(cc1)F)c1-c1ncccn1)=O Chemical compound OC(c(cc(cc1)F)c1-c1ncccn1)=O GWFSRJKDYXADOG-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4192—1,2,3-Triazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/428—Thiazoles condensed with carbocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/535—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 oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/12—Antidiarrhoeals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
- A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/06—Antiarrhythmics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Heart & Thoracic Surgery (AREA)
- Endocrinology (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Reproductive Health (AREA)
- Physical Education & Sports Medicine (AREA)
- Pulmonology (AREA)
- Anesthesiology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Child & Adolescent Psychology (AREA)
- Gastroenterology & Hepatology (AREA)
- Emergency Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25450909P | 2009-10-23 | 2009-10-23 | |
| US61/254,509 | 2009-10-23 |
Related Child Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020177034281A Division KR101859409B1 (ko) | 2009-10-23 | 2010-10-21 | 오렉신 수용체 조절제로서의 이치환된 옥타하이드로피롤로[3,4-c]피롤 |
| KR1020177034279A Division KR101859400B1 (ko) | 2009-10-23 | 2010-10-21 | 오렉신 수용체 조절제로서의 이치환된 옥타하이드로피롤로[3,4-c]피롤 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20120105449A true KR20120105449A (ko) | 2012-09-25 |
Family
ID=43385633
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020177034281A Active KR101859409B1 (ko) | 2009-10-23 | 2010-10-21 | 오렉신 수용체 조절제로서의 이치환된 옥타하이드로피롤로[3,4-c]피롤 |
| KR1020177034279A Active KR101859400B1 (ko) | 2009-10-23 | 2010-10-21 | 오렉신 수용체 조절제로서의 이치환된 옥타하이드로피롤로[3,4-c]피롤 |
| KR1020127013101A Withdrawn KR20120105449A (ko) | 2009-10-23 | 2010-10-21 | 오렉신 수용체 조절제로서의 이치환된 옥타하이드로피롤로[3,4-c]피롤 |
Family Applications Before (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020177034281A Active KR101859409B1 (ko) | 2009-10-23 | 2010-10-21 | 오렉신 수용체 조절제로서의 이치환된 옥타하이드로피롤로[3,4-c]피롤 |
| KR1020177034279A Active KR101859400B1 (ko) | 2009-10-23 | 2010-10-21 | 오렉신 수용체 조절제로서의 이치환된 옥타하이드로피롤로[3,4-c]피롤 |
Country Status (38)
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20220136475A (ko) * | 2016-03-10 | 2022-10-07 | 얀센 파마슈티카 엔.브이. | 오렉신-2 수용체 길항제를 사용한 우울증의 치료 방법 |
| US12378254B2 (en) | 2009-10-23 | 2025-08-05 | Janssen Pharmaceutica Nv | Disubstituted octahydropyrrolo[3,4-c]pyrroles as orexin receptor modulators |
Families Citing this family (64)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9586962B2 (en) | 2011-04-20 | 2017-03-07 | Janssen Pharmaceutica Nv | Disubstituted octahydropyrrolo [3,4-C] pyrroles as orexin receptor modulators |
| US8501768B2 (en) * | 2011-05-17 | 2013-08-06 | Hoffmann-La Roche Inc. | Hexahydrocyclopentapyrrolone, hexahydropyrrolopyrrolone, octahydropyrrolopyridinone and octahydropyridinone compounds |
| MX343837B (es) | 2011-11-08 | 2016-11-24 | Actelion Pharmaceuticals Ltd | Derivados de 2 - (1,2,3 -triazol - 2 - il) benzamida y 3 - (1,2,3 - triazol - 2 - il) picolinamida. |
| US9440982B2 (en) | 2012-02-07 | 2016-09-13 | Eolas Therapeutics, Inc. | Substituted prolines/piperidines as orexin receptor antagonists |
| WO2013119639A1 (en) | 2012-02-07 | 2013-08-15 | Eolas Therapeutics, Inc. | Substituted prolines / piperidines as orexin receptor antagonists |
| ES2617863T3 (es) | 2012-06-04 | 2017-06-20 | Actelion Pharmaceuticals Ltd. | Derivados de bencimidazol-prolina |
| US9682966B2 (en) * | 2012-08-16 | 2017-06-20 | The Scripps Research Institute | Kappa opioid ligands |
| SG11201502493XA (en) | 2012-10-10 | 2015-04-29 | Actelion Pharmaceuticals Ltd | Orexin receptor antagonists which are [ortho bi (hetero )aryl]-[2-(meta bi (hetero )aryl)-pyrrolidin-1-yl]-methanone derivatives |
| CN103012293A (zh) * | 2012-12-13 | 2013-04-03 | 同济大学 | 一种抗失眠药物mk-4305中间体的合成方法 |
| CA2902135A1 (en) | 2013-03-12 | 2014-09-18 | Actelion Pharmaceuticals Ltd | Azetidine amide derivatives as orexin receptor antagonists |
| TW201444849A (zh) | 2013-03-13 | 2014-12-01 | Janssen Pharmaceutica Nv | 經取代的7-氮雜雙環類及其作為食慾激素受體調節劑之用途 |
| TW201444821A (zh) | 2013-03-13 | 2014-12-01 | Janssen Pharmaceutica Nv | 經取代之哌啶化合物及其作為食慾素受體調節劑之用途 |
| TWI621618B (zh) | 2013-03-13 | 2018-04-21 | 比利時商健生藥品公司 | 經取代2-氮雜雙環類及其作為食慾素受體調控劑之用途 |
| JP6647592B2 (ja) * | 2013-07-03 | 2020-02-14 | ルンドベック ラ ホーヤ リサーチ センター,インク. | ピロロピロールカルバメート、および関連する有機化合物、医薬組成物、ならびにその医学的使用 |
| ES2696708T3 (es) | 2013-12-04 | 2019-01-17 | Idorsia Pharmaceuticals Ltd | Uso de derivados de bencimidazol-prolina |
| WO2016020403A1 (en) * | 2014-08-04 | 2016-02-11 | Sandoz Ag | Preparation of a benzoic acid derivative and its use for the preparation of suvorexant |
| US10221170B2 (en) | 2014-08-13 | 2019-03-05 | Eolas Therapeutics, Inc. | Difluoropyrrolidines as orexin receptor modulators |
| MX2017003254A (es) | 2014-09-11 | 2017-10-12 | Janssen Pharmaceutica Nv | 2-azabiciclos sustituidos y su uso como moduladores de receptores de orexina. |
| US10196383B2 (en) | 2015-07-17 | 2019-02-05 | Sunshine Lake Pharma Co., Ltd. | Substituted quinazoline compounds and preparation and uses thereof |
| CA3005918C (en) * | 2015-11-23 | 2023-10-17 | Sunshine Lake Pharma Co., Ltd. | Octahydropyrrolo[3,4-c]pyrrole derivatives and uses thereof |
| WO2017088731A1 (zh) * | 2015-11-24 | 2017-06-01 | 广东东阳光药业有限公司 | 八氢吡咯并[3,4-c]吡咯衍生物及其用途 |
| DK3414241T3 (da) | 2016-02-12 | 2022-08-01 | Astrazeneca Ab | Halogensubstituerede piperidiner som orexinreceptormodulatorer |
| WO2017197192A1 (en) | 2016-05-12 | 2017-11-16 | Abide Therapeutics, Inc. | Spirocycle compounds and methods of making and using same |
| CN105949203B (zh) * | 2016-05-24 | 2018-07-13 | 广东东阳光药业有限公司 | 八氢吡咯并[3,4-c]吡咯衍生物及其使用方法和用途 |
| CN107759620B (zh) * | 2016-08-16 | 2021-11-12 | 广东东阳光药业有限公司 | 八氢吡咯并[3,4-c]吡咯衍生物及其使用方法和用途 |
| JOP20190107A1 (ar) | 2016-11-16 | 2019-05-09 | Lundbeck La Jolla Research Center Inc | مثبطات أحادي أسيل جليسرول ليباز (magl) |
| CN108299437B (zh) * | 2017-01-13 | 2022-07-08 | 广东东阳光药业有限公司 | 八氢吡咯并[3,4-c]吡咯衍生物及其用途 |
| GB201702174D0 (en) * | 2017-02-09 | 2017-03-29 | Benevolentai Bio Ltd | Orexin receptor antagonists |
| SI3619199T1 (sl) | 2017-05-03 | 2021-11-30 | Idorsia Pharmaceuticals Ltd | Priprava derivatov 2-((1,2,3)triazol-2-il)-benzojske kisline |
| GB201707504D0 (en) * | 2017-05-10 | 2017-06-21 | Benevolentai Bio Ltd | Orexin receptor antagonists |
| GB201707499D0 (en) * | 2017-05-10 | 2017-06-21 | Benevolentai Bio Ltd | Orexin receptor antagonists |
| CN111050765B (zh) | 2017-08-29 | 2024-01-02 | H.隆德贝克有限公司 | 螺环化合物及其制造和使用方法 |
| JP7177825B2 (ja) | 2017-08-29 | 2022-11-24 | ハー・ルンドベック・アクチエゼルスカベット | スピロ環化合物並びにその作製及び使用方法 |
| CN111132975B (zh) | 2017-09-28 | 2023-05-23 | 勃林格殷格翰国际有限公司 | N-(2,2-二氟乙基)-n-[(嘧啶基氨基)丙基]芳基甲酰胺 |
| CN109988171A (zh) * | 2017-12-29 | 2019-07-09 | 广东东阳光药业有限公司 | 八氢吡咯并[3,4-c]吡咯衍生物及其用途 |
| CN109988170B (zh) * | 2017-12-29 | 2022-04-26 | 广东东阳光药业有限公司 | 八氢吡咯并[3,4-c]吡咯衍生物及其用途 |
| CN109988169B (zh) * | 2017-12-29 | 2022-02-01 | 广东东阳光药业有限公司 | 八氢吡咯并[3,4-c]吡咯衍生物及其用途 |
| GB201809295D0 (en) | 2018-06-06 | 2018-07-25 | Institute Of Cancer Res Royal Cancer Hospital | Lox inhibitors |
| US20210169883A1 (en) * | 2018-07-27 | 2021-06-10 | Icahn School Of Medicine At Mount Sinai | Method of treating aggression with orexin receptor antagonists |
| JP7398452B2 (ja) | 2018-11-14 | 2023-12-14 | ヤンセン ファーマシューティカ エヌ.ベー. | オレキシン受容体調節因子としての縮合複素環式化合物を作製する改良された合成方法 |
| GB201818750D0 (en) | 2018-11-16 | 2019-01-02 | Institute Of Cancer Res Royal Cancer Hospital | Lox inhibitors |
| CN112142713A (zh) * | 2019-06-27 | 2020-12-29 | 山东润博生物科技有限公司 | 一种咪草烟的合成方法 |
| US20220289754A1 (en) * | 2019-08-07 | 2022-09-15 | Janssen Pharmaceutica Nv | Improved synthetic methods of making (2h-1, 2, 3-triazol-2-yl) phenyl compounds as orexin receptor modulators |
| CN112876480B (zh) * | 2019-11-29 | 2022-07-26 | 广东东阳光药业有限公司 | 八氢吡咯并[3,4-c]吡咯衍生物的晶型 |
| CN112876479B (zh) * | 2019-11-29 | 2022-07-26 | 广东东阳光药业有限公司 | 八氢吡咯并[3,4-c]吡咯衍生物的晶型 |
| CN112876478B (zh) * | 2019-11-29 | 2022-07-26 | 广东东阳光药业有限公司 | 八氢吡咯并[3,4-c]吡咯衍生物的晶型 |
| CN112876481B (zh) * | 2019-11-29 | 2022-07-26 | 广东东阳光药业有限公司 | 八氢吡咯并[3,4-c]吡咯衍生物的晶型 |
| WO2021104294A1 (en) * | 2019-11-29 | 2021-06-03 | Sunshine Lake Pharma Co., Ltd. | CRYSTAL FORMS OF OCTAHYDROPYRROLO [3,4-c] PYRROLE DERIVATIVES |
| WO2022122009A1 (zh) * | 2020-12-11 | 2022-06-16 | 苏州晶云药物科技股份有限公司 | 吡咯类衍生化合物的晶型及其制备方法 |
| AU2022239403A1 (en) * | 2021-03-16 | 2023-09-21 | Jiangsu Hansoh Pharmaceutical Group Co., Ltd. | Nitrogen-containing heterocyclic polycyclic compound, preparation method therefor, and application thereof |
| CN114063673B (zh) * | 2021-11-09 | 2023-03-03 | 万华化学集团股份有限公司 | 一种反应釜温度控制方法、系统及存储介质 |
| CN116217593B (zh) * | 2021-12-02 | 2025-05-09 | 江苏恩华药业股份有限公司 | 一种八氢吡咯并[3,4-c]吡咯甲基酮衍生物及其应用 |
| WO2023163964A1 (en) | 2022-02-24 | 2023-08-31 | Teva Czech Industries S.R.O. | Solid state forms of seltorexant |
| WO2023180556A1 (en) | 2022-03-24 | 2023-09-28 | Janssen Pharmaceutica Nv | Methods for treating agitation in subjects with mild cognitive impairment or major neurocognition disorder |
| AU2023308205A1 (en) * | 2022-07-15 | 2025-01-30 | Biogen Ma Inc. | Emopamil-binding protein inhibitors and uses thereof |
| CA3266204A1 (en) * | 2022-09-14 | 2025-03-19 | Shanghai Hansoh Biomedical Co., Ltd. | FREE CRYSTALLINE BASIC FORM OF A POLYCYCLIC NITROGEN HETEROCYCLE COMPOUND AND ITS PREPARATION PROCESS |
| WO2024109672A1 (zh) * | 2022-11-23 | 2024-05-30 | 江苏恩华药业股份有限公司 | 一种二取代八氢吡咯并[3,4-c]吡咯甲基酮衍生物及其应用 |
| WO2024125395A1 (zh) * | 2022-12-12 | 2024-06-20 | 江苏恩华药业股份有限公司 | 一种取代四氢环戊基[c]吡咯衍生物、制备方法、中间体及其应用 |
| WO2024189472A1 (en) | 2023-03-14 | 2024-09-19 | Janssen Pharmaceutica Nv | Improved synthetic methods of making substituted pyrimidine intermediates for synthesis of orexin receptor modulators |
| WO2025003991A1 (en) | 2023-06-29 | 2025-01-02 | Janssen Pharmaceutica Nv | Method of treating depression using seltorexant |
| WO2025162233A1 (zh) * | 2024-01-29 | 2025-08-07 | 成都康弘药业集团股份有限公司 | 食欲素受体调节剂及其制备方法和用途 |
| WO2025242852A1 (en) | 2024-05-24 | 2025-11-27 | Janssen Pharmaceutica Nv | Seltorexant for use in treating major depressive disorder with insomnia symptoms |
| CN118580243B (zh) * | 2024-08-07 | 2025-01-03 | 艾斯拓康生物医药(天津)有限公司 | 一类含氮并环化合物及其制备方法和应用 |
| CN119039301B (zh) * | 2024-10-31 | 2025-09-02 | 江苏豪森药业集团有限公司 | 一种含氮杂环的多环化合物晶型ⅰ的制备方法 |
Family Cites Families (152)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL7503310A (nl) | 1975-03-20 | 1976-09-22 | Philips Nv | Verbindingen met antidepressieve werking. |
| GB1526331A (en) | 1976-01-14 | 1978-09-27 | Kefalas As | Phthalanes |
| IL122296A0 (en) | 1995-06-06 | 1998-04-05 | Abbott Lab | Quinolizinone type compounds |
| GB9519563D0 (en) | 1995-09-26 | 1995-11-29 | Merck Sharp & Dohme | Therapeutic agents |
| WO2000055143A1 (en) | 1999-03-17 | 2000-09-21 | F. Hoffmann-La Roche Ag | Oxazolone derivatives and their use as alpha-1 adrenoreceptor modulators |
| US6375897B1 (en) | 2000-02-14 | 2002-04-23 | Ansys Technologies, Inc. | Urine collection cup |
| MY145722A (en) | 2000-04-27 | 2012-03-30 | Abbott Lab | Diazabicyclic central nervous system active agents |
| US6809105B2 (en) | 2000-04-27 | 2004-10-26 | Abbott Laboratories | Diazabicyclic central nervous system active agents |
| CA2408343A1 (en) | 2000-05-11 | 2002-11-07 | Banyu Pharmaceutical Co., Ltd. | N-acyltetrahydroisoquinoline derivatives |
| SE0100326D0 (sv) | 2001-02-02 | 2001-02-02 | Astrazeneca Ab | New compounds |
| WO2002070527A1 (en) | 2001-03-02 | 2002-09-12 | Akzo Nobel N.V. | Mass-selective purification of organometallics |
| EP1368354A1 (en) | 2001-03-07 | 2003-12-10 | Pfizer Products Inc. | Modulators of chemokine receptor activity |
| IL159041A0 (en) | 2001-06-28 | 2004-05-12 | Smithkline Beecham Plc | N-aroyl cyclic amine derivatives as orexin receptor antagonists |
| US6455722B1 (en) | 2001-06-29 | 2002-09-24 | Pabu Services, Inc. | Process for the production of pentaerythritol phosphate alcohol |
| GB2383315B (en) | 2001-12-18 | 2005-04-06 | Christopher Donald Clarke | Vehicle imaging system |
| GB0130341D0 (en) | 2001-12-19 | 2002-02-06 | Smithkline Beecham Plc | Compounds |
| DE10226943A1 (de) | 2002-06-17 | 2004-01-08 | Bayer Ag | Phenylaminopyrimidine und ihre Verwendung |
| CA2460051A1 (en) * | 2002-07-09 | 2004-01-15 | Actelion Pharmaceuticals Ltd. | 7,8,9,10-tetrahydro-6h-azepino, 6,7,8,9-tetrahydro-pyrido and 2,3-dihydro-2h-pyrrolo[2,1-b]-quinazolinone derivatives |
| ATE496884T1 (de) | 2002-10-11 | 2011-02-15 | Actelion Pharmaceuticals Ltd | Sulphonylaminoessigsaeure derivate und deren verwendung als orexin rezeptor antagoniste |
| GB0225944D0 (en) | 2002-11-06 | 2002-12-11 | Glaxo Group Ltd | Novel compounds |
| JP4637089B2 (ja) | 2003-03-26 | 2011-02-23 | アクテリオン ファーマシューティカルズ リミテッド | アセトアミド誘導体 |
| ATE383345T1 (de) | 2003-04-28 | 2008-01-15 | Actelion Pharmaceuticals Ltd | Quinoxalin-3-on-verdindungen als orexin-rezeptor antagonisten. |
| US20040242641A1 (en) | 2003-05-27 | 2004-12-02 | Buckley Michael J. | (1S,5S)-3-(5,6-dichloro-3-pyridinyl)-3,6-diazabicyclo[3.2.0]heptane is an effective analgesic agent |
| WO2005005439A1 (en) | 2003-07-09 | 2005-01-20 | Suven Life Sciences Limited | Benzothiazino indoles |
| TW200507850A (en) | 2003-07-25 | 2005-03-01 | Kyowa Hakko Kogyo Kk | Pharmaceutical composition |
| WO2005023231A1 (en) | 2003-09-10 | 2005-03-17 | MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. | Polypyrimidine tract binding protein promotes insulin secretory granule biogenesis |
| US20050065178A1 (en) | 2003-09-19 | 2005-03-24 | Anwer Basha | Substituted diazabicycloakane derivatives |
| US7399765B2 (en) | 2003-09-19 | 2008-07-15 | Abbott Laboratories | Substituted diazabicycloalkane derivatives |
| US20050176680A1 (en) | 2003-12-11 | 2005-08-11 | Sepracor, Inc. | Combination of sedative and a neurotransmitter modulator, and methods for improving sleep quality and treating depression |
| HUP0400405A3 (en) | 2004-02-10 | 2009-03-30 | Sanofi Synthelabo | Pyrimidine derivatives, process for producing them, their use, pharmaceutical compositions containing them and their intermediates |
| HRP20150371T1 (hr) | 2004-03-01 | 2015-05-08 | Actelion Pharmaceuticals Ltd. | Supstituirani derivati 1,2,3,4-tetrahidroizokinolina |
| JP4845873B2 (ja) | 2004-03-03 | 2011-12-28 | ケモセントリックス インコーポレーティッド | 二環式および架橋した窒素複素環 |
| US7435831B2 (en) | 2004-03-03 | 2008-10-14 | Chemocentryx, Inc. | Bicyclic and bridged nitrogen heterocycles |
| CN101065385A (zh) | 2004-07-22 | 2007-10-31 | 坎布里制药公司 | 治疗微生物感染的利福霉素衍生物 |
| JP2008507543A (ja) | 2004-07-22 | 2008-03-13 | グラクソ グループ リミテッド | 抗細菌剤 |
| FR2874011B1 (fr) | 2004-08-03 | 2007-06-15 | Sanofi Synthelabo | Derives de sulfonamides, leur preparation et leur application en therapeutique |
| EP1807390A4 (en) | 2004-11-04 | 2008-07-02 | Neurogen Corp | ARYL ALKYL UREA AS CB1 ANTAGONISTS |
| CA2587141A1 (en) | 2004-11-24 | 2006-06-01 | Pfizer Inc. | Octahydropyrrolo[3,4-c]pyrrole derivatives |
| DE102004061344A1 (de) | 2004-12-20 | 2006-07-06 | Siemens Ag | Verfahren zur sicheren Auslegung eines Systems, zugehörige Systemkomponente und Software |
| WO2006124748A2 (en) * | 2005-05-13 | 2006-11-23 | Lexicon Genetics Incorporated | Multicyclic compounds and methods of their use |
| WO2006124897A2 (en) | 2005-05-13 | 2006-11-23 | Lexicon Genetics Incorporated | Methods and compositions for improving cognition |
| GB0510204D0 (en) | 2005-05-19 | 2005-06-22 | Chroma Therapeutics Ltd | Enzyme inhibitors |
| US20080175795A1 (en) | 2005-06-30 | 2008-07-24 | Bexel Pharmaceuticals, Inc. | Novel derivatives of amino acids for treatment of obesity and related disorders |
| GB0514018D0 (en) | 2005-07-07 | 2005-08-17 | Ionix Pharmaceuticals Ltd | Chemical compounds |
| CA2620124A1 (en) | 2005-08-26 | 2007-03-01 | Merck And Co., Inc. | Diazaspirodecane orexin receptor antagonists |
| FR2896798A1 (fr) | 2006-01-27 | 2007-08-03 | Sanofi Aventis Sa | Derives de sulfonamides, leur preparation et leur application en therapeutique |
| FR2896799B1 (fr) | 2006-02-02 | 2008-03-28 | Sanofi Aventis Sa | Derives de sulfonamides, leur preparation et leur application en therapeutique |
| US7553836B2 (en) | 2006-02-06 | 2009-06-30 | Bristol-Myers Squibb Company | Melanin concentrating hormone receptor-1 antagonists |
| EP2001485B1 (en) | 2006-03-29 | 2015-09-09 | Merck Sharp & Dohme Corp. | Diazepan orexin receptor antagonists |
| US20090105318A1 (en) | 2006-03-29 | 2009-04-23 | Coleman Paul J | Amidoethylthioether Orexin Receptor Antagonists |
| US7834028B2 (en) | 2006-04-26 | 2010-11-16 | Actelion Pharmaceuticals Ltd. | Pyrazolo-tetrahydro pyridine derivatives as orexin receptor antagonists |
| WO2007146761A2 (en) | 2006-06-12 | 2007-12-21 | Neurogen Corporation | Diaryl pyrimidinones and related compounds |
| DE602007008434D1 (de) * | 2006-07-14 | 2010-09-23 | Merck Sharp & Dohme | Rezeptoren |
| US20100029736A1 (en) | 2006-07-14 | 2010-02-04 | Merck & Co., Inc. | 2-substituted proline bis-amide orexin receptor antagonists |
| EP2049110B1 (en) | 2006-07-14 | 2014-08-20 | Merck Sharp & Dohme Corp. | Bridged diazepan orexin receptor antagonists |
| DE602007012910D1 (de) | 2006-08-15 | 2011-04-14 | Actelion Pharmaceuticals Ltd | Azetidinverbindungen als orexin-rezeptor-antagonisten |
| US20100029617A1 (en) | 2006-08-28 | 2010-02-04 | Actelion Pharmaceuticals Ltd. | 1,4,5,6,7,8-hexahydro-1,2,5-triaza-azulene derivatives as orexin receptor antagonists |
| ES2345130T3 (es) | 2006-09-18 | 2010-09-15 | F. Hoffmann-La Roche Ag | Derivados de octahidropirrolo(3,4-c)pirrol y su uso como antiviricos. |
| ES2350460T3 (es) | 2006-09-29 | 2011-01-24 | Actelion Pharmaceuticals Ltd. | Derivados de 3-aza-biciclo[3.1.0]hexano. |
| US20100105614A1 (en) | 2006-10-25 | 2010-04-29 | Somaxon Pharmaceuticals, Inc. | Ultra low dose doxepin and methods of using the same to treat sleep disorders |
| WO2008067121A2 (en) | 2006-11-07 | 2008-06-05 | Lexicon Pharmaceuticals, Inc. | Methods of treating cognitive impairment and dementia |
| PE20081229A1 (es) | 2006-12-01 | 2008-08-28 | Merck & Co Inc | Antagonistas de receptor de orexina de diazepam sustituido |
| US20110077200A1 (en) | 2006-12-06 | 2011-03-31 | Somaxon Pharmaceuticals, Inc. | Combination therapy using low-dose doxepin for the improvement of sleep |
| AU2007337659A1 (en) | 2006-12-22 | 2008-07-03 | Actelion Pharmaceuticals Ltd. | 5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine derivatives |
| CL2008000836A1 (es) | 2007-03-26 | 2008-11-07 | Actelion Pharmaceuticals Ltd | Compuestos derivados de tiazolidina, antagonistas del receptor de orexina; composicion farmaceutica que los comprende; y su uso en el tratamiento de neurosis emocional, depresion grave, trastornos psicoticos, alzheimer, parkinson, dolor, entre otras. |
| CN101687882A (zh) | 2007-04-25 | 2010-03-31 | 百时美施贵宝公司 | 非碱性黑色素浓集激素受体-1拮抗剂 |
| EP2150114A4 (en) | 2007-05-18 | 2012-01-18 | Merck Sharp & Dohme | OXO-BRIDGED DIAZEPANOREXINE RECEPTOR ANTAGONISTS |
| FR2918061B1 (fr) * | 2007-06-28 | 2010-10-22 | Sanofi Aventis | Derives de 6-cycloamino-3-(pyridin-4-yl)imidazo°1,2-b!- pyridazine,leur preparation et leur application en therapeutique. |
| GB0712888D0 (en) | 2007-07-03 | 2007-08-15 | Glaxo Group Ltd | Novel compounds |
| BRPI0813218A2 (pt) | 2007-07-03 | 2014-12-23 | Actelion Pharmaceuticals Ltd | Composto, composição farmacêutica que o contém como princípio ativo e uso do composto. |
| PE20090441A1 (es) | 2007-07-03 | 2009-05-08 | Glaxo Group Ltd | DERIVADOS DE IMIDAZO[1,2-a]PIRIDIN-2-ILMETIL PIPERIDINA SUSTITUIDA |
| US20090011994A1 (en) | 2007-07-06 | 2009-01-08 | Bristol-Myers Squibb Company | Non-basic melanin concentrating hormone receptor-1 antagonists and methods |
| WO2009011775A1 (en) | 2007-07-13 | 2009-01-22 | Merck & Co., Inc. | Amidoethyl alkylamino orexin receptor antagonists |
| FR2918986B1 (fr) * | 2007-07-19 | 2009-09-04 | Sanofi Aventis Sa | Derives de 6-cycloamino-3-(pyridazin-4-yl)imidazo[1,2-b]- pyridazine, leur preparation et leur application en therapeutique |
| KR20100046047A (ko) | 2007-07-27 | 2010-05-04 | 액테리온 파마슈티칼 리미티드 | 2-아자-비시클로[3.3.0]옥탄 유도체 |
| CN101801918A (zh) | 2007-08-02 | 2010-08-11 | 弗·哈夫曼-拉罗切有限公司 | 作为食欲肽受体拮抗剂的单酰胺衍生物 |
| AU2008288151A1 (en) | 2007-08-15 | 2009-02-19 | Actelion Pharmaceuticals Ltd | 1,2-diamido-ethylene derivatives as orexin antagonists |
| WO2009040730A2 (en) | 2007-09-24 | 2009-04-02 | Actelion Pharmaceuticals Ltd | Pyrrolidines and piperidines as orexin receptor antagonists |
| JP2011502146A (ja) | 2007-10-29 | 2011-01-20 | メルク・シャープ・エンド・ドーム・コーポレイション | 置換ジアゼパンオレキシン受容体アンタゴニスト |
| DE102007052177A1 (de) | 2007-10-30 | 2009-05-07 | Novega Produktionssysteme Gmbh | Ortungsbake |
| EP2058001A1 (en) | 2007-11-08 | 2009-05-13 | Crossbeta Biosciences B.V. | Enhancement of immunogenicity of antigens |
| AU2008339572B2 (en) | 2007-12-21 | 2012-05-10 | Astrazeneca Ab | Bicyclic derivatives for use in the treatment of androgen receptor associated conditions |
| CN101903372B (zh) | 2007-12-21 | 2014-06-18 | 弗·哈夫曼-拉罗切有限公司 | 作为食欲肽受体拮抗剂的杂芳基衍生物 |
| GB0806536D0 (en) | 2008-04-10 | 2008-05-14 | Glaxo Group Ltd | Novel compounds |
| AU2009251816B2 (en) | 2008-05-27 | 2015-12-10 | Intra-Cellular Therapies, Inc. | Methods and compositions for sleep disorders and other disorders |
| MX2011000462A (es) | 2008-07-29 | 2011-04-05 | Hoffmann La Roche | Pirrolidin-3-ilmetil-amina como antagonista de orexina. |
| AR072899A1 (es) | 2008-08-07 | 2010-09-29 | Merck Sharp & Dohme | Derivados de terpiridina-carboxamida antagonistas de receptores de orexina, composiciones farmaceuticas que los contienen y uso de los mismos en el tratamiento del insomnio y la obesidad. |
| US20100267730A1 (en) | 2008-10-09 | 2010-10-21 | Giuseppe Alvaro | Novel compounds |
| US8093255B2 (en) | 2008-10-09 | 2012-01-10 | Glaxo Group Limited | Imidazo[1,2-A]pyrimidines as orexin receptor antagonists |
| US8129384B2 (en) | 2008-10-09 | 2012-03-06 | Glaxo Group Limited | Imidazo[1,2-a]pyrazines as orexin receptor antagonists |
| CA2739917A1 (en) | 2008-10-21 | 2010-04-29 | Merck Sharp & Dohme Corp. | 2,5-disubstituted morpholine orexin receptor antagonists |
| EP2349269A4 (en) | 2008-10-21 | 2012-04-25 | Merck Sharp & Dohme | 2,5-DISUBSTITUTED PIPERIDINOREXINE RECEPTOR ANTAGONISTS |
| JP2012506374A (ja) | 2008-10-21 | 2012-03-15 | メルク・シャープ・エンド・ドーム・コーポレイション | 2,5−二置換ピペリジンオレキシン受容体アンタゴニスト |
| CA2739927A1 (en) | 2008-10-21 | 2010-04-29 | Merck Sharp & Dohme Corp. | Disubstituted azepan orexin receptor antagonists |
| AU2009307920A1 (en) | 2008-10-21 | 2010-04-29 | Merck Sharp & Dohme Corp. | 2,3-disubstituted piperidine orexin receptor antagonists |
| WO2010048014A1 (en) | 2008-10-21 | 2010-04-29 | Merck Sharp & Dohme Corp. | 2,4-disubstituted pyrrolidine orexin receptor antagonists |
| WO2010051238A1 (en) | 2008-10-30 | 2010-05-06 | Merck Sharp & Dohme Corp. | Pyridazine carboxamide orexin receptor antagonists |
| US8399494B2 (en) | 2008-10-30 | 2013-03-19 | Merck Sharp & Dohme Corp. | 2,5-disubstituted phenyl carboxamide orexin receptor antagonists |
| EP2350010B1 (en) | 2008-10-30 | 2014-03-26 | Merck Sharp & Dohme Corp. | Isonicotinamide orexin receptor antagonists |
| WO2010060470A1 (en) | 2008-11-26 | 2010-06-03 | Glaxo Group Limited | Piperidine derivatives useful as orexin receptor antagonists |
| EP2358712A1 (en) | 2008-11-26 | 2011-08-24 | Glaxo Group Limited | Piperidine derivatives useful as orexin receptor antagonists |
| EP2358713A1 (en) | 2008-11-26 | 2011-08-24 | Glaxo Group Limited | Imidazopyridazine derivatives acting as orexin antagonists |
| KR20110091581A (ko) | 2008-12-02 | 2011-08-11 | 글락소 그룹 리미티드 | N-{[1r,4s,6r-3-(2-피리디닐카르보닐)-3-아자비시클로[4.1.0]헵트-4-일]메틸}-2-헤테로아릴아민 유도체 및 그의 용도 |
| MX2011005800A (es) | 2008-12-02 | 2011-06-20 | Glaxo Group Ltd | Derivados de n{[(1r,4s,6r)-3-(2-piridinilcarbonil)-3-azabiciclo[4. 1.0]hept-4-il]metil}-2-heteroarilamina y sus usos. |
| GB0823467D0 (en) | 2008-12-23 | 2009-01-28 | Glaxo Group Ltd | Novel Compounds |
| US20100214135A1 (en) | 2009-02-26 | 2010-08-26 | Microsoft Corporation | Dynamic rear-projected user interface |
| EA201171293A1 (ru) | 2009-04-24 | 2012-05-30 | Глэксо Груп Лимитед | 3-азабицикло[4.1.0]гептаны, применяемые в качестве антагонистов орексина |
| WO2011023578A1 (en) | 2009-08-24 | 2011-03-03 | Glaxo Group Limited | 5-methyl-piperidine derivatives as orexin receptor antagonists for the treatment of sleep disorder |
| US20120149711A1 (en) | 2009-08-24 | 2012-06-14 | Glaxo Group Limited | Piperidine derivatives used as orexin antagonists |
| EP2491034B1 (en) | 2009-10-23 | 2013-12-18 | Janssen Pharmaceutica, N.V. | Fused heterocyclic compounds as orexin receptor modulators |
| US9062044B2 (en) | 2009-10-23 | 2015-06-23 | Janssen Pharmaceutica Nv | Disubstituted octahydropyrrolo[3,4-c]pyrroles as orexin receptor modulators |
| EP2491038B1 (en) | 2009-10-23 | 2016-04-06 | Janssen Pharmaceutica N.V. | Disubstituted octahy - dropyrrolo [3,4-c]pyrroles as orexin receptor modulators |
| US8877773B2 (en) | 2009-10-24 | 2014-11-04 | Indiana University Research And Technology Corporation | Methods for treating chronic obstructive pulmonary disease |
| TWI410630B (zh) | 2009-11-10 | 2013-10-01 | Ct Lab Inc | 一種用以治療與食慾素受體1、食慾素受體2、體抑素受體2或多巴胺d2l受體相關之疾病的方法和組合物 |
| WO2011079274A1 (en) | 2009-12-23 | 2011-06-30 | Jasco Pharmaceuticals, LLC | Aminopyrimidine kinase inhibitors |
| WO2012081692A1 (ja) | 2010-12-17 | 2012-06-21 | 大正製薬株式会社 | ピラゾール誘導体 |
| WO2012089606A1 (en) | 2010-12-28 | 2012-07-05 | Glaxo Group Limited | Azabicyclo [4.1.0] hept - 4 - yl derivatives as human orexin receptor antagonists |
| WO2012089607A1 (en) | 2010-12-28 | 2012-07-05 | Glaxo Group Limited | Novel compounds with a 3a-azabicyclo [4.1.0] heptane core acting on orexin receptors |
| US9586962B2 (en) | 2011-04-20 | 2017-03-07 | Janssen Pharmaceutica Nv | Disubstituted octahydropyrrolo [3,4-C] pyrroles as orexin receptor modulators |
| WO2012153729A1 (ja) | 2011-05-10 | 2012-11-15 | 大正製薬株式会社 | ヘテロ芳香環誘導体 |
| US20140228377A1 (en) | 2011-07-05 | 2014-08-14 | Taisho Pharmaceutical Co., Ltd. | Methylpiperidine derivative |
| EP2768305A4 (en) | 2011-10-21 | 2015-04-29 | Merck Sharp & Dohme | 2,5-DISUBSTITUTED THIOMORPHOLIN OREXINE RECEPTOR ANTAGONISTS |
| WO2013119639A1 (en) | 2012-02-07 | 2013-08-15 | Eolas Therapeutics, Inc. | Substituted prolines / piperidines as orexin receptor antagonists |
| US9440982B2 (en) | 2012-02-07 | 2016-09-13 | Eolas Therapeutics, Inc. | Substituted prolines/piperidines as orexin receptor antagonists |
| ES2656972T3 (es) | 2012-02-23 | 2018-03-01 | Vanderbilt University | Análogos de 5-aminotieno [2,3-c] piridazin-6-carboxamida como moduladores alostéricos positivos del receptor de acetilcolina muscarínico M4 |
| JP2014015452A (ja) | 2012-06-15 | 2014-01-30 | Taisho Pharmaceutical Co Ltd | ピラゾール誘導体を含有する医薬 |
| SG11201408316SA (en) | 2012-06-15 | 2015-03-30 | Taisho Pharmaceutical Co Ltd | Branched chain alkyl heteroaromatic ring derivative |
| BR112014031360B1 (pt) | 2012-06-15 | 2022-04-12 | Taisho Pharmaceutical Co., Ltd | Composto, composição farmacêutica e medicamento terapêutico ou preventivo |
| JP2014111586A (ja) | 2012-11-09 | 2014-06-19 | Taisho Pharmaceutical Co Ltd | ヘテロ芳香環誘導体を含有する医薬 |
| WO2014085208A1 (en) | 2012-11-27 | 2014-06-05 | Merck Sharp & Dohme Corp. | 2-pyridylamino-4-nitrile-piperidinyl orexin receptor antagonists |
| JP2016028017A (ja) | 2012-12-13 | 2016-02-25 | 大正製薬株式会社 | フッ素置換ピペリジン化合物 |
| JP2014141480A (ja) | 2012-12-28 | 2014-08-07 | Taisho Pharmaceutical Co Ltd | メチルピペリジン誘導体を含有する医薬 |
| TWI621618B (zh) | 2013-03-13 | 2018-04-21 | 比利時商健生藥品公司 | 經取代2-氮雜雙環類及其作為食慾素受體調控劑之用途 |
| WO2015018027A1 (en) | 2013-08-08 | 2015-02-12 | Merck Sharp & Dohme Corp. | Thiazole orexin receptor antagonists |
| US9956227B2 (en) | 2013-12-03 | 2018-05-01 | Intra-Cellular Therapies, Inc. | Method for the treatment of residual symptoms of schizophrenia |
| US9586934B2 (en) | 2013-12-09 | 2017-03-07 | Merck Sharp & Dohme Corp. | 2-pyridyloxy-4-methyl orexin receptor antagonists |
| JP2015131802A (ja) | 2013-12-13 | 2015-07-23 | 大正製薬株式会社 | 分岐鎖アルキルヘテロ芳香環誘導体を含有する医薬 |
| JP5930010B2 (ja) | 2013-12-13 | 2016-06-08 | 大正製薬株式会社 | ヘテロ芳香環メチル環状アミン誘導体を含有する医薬 |
| US9617246B2 (en) | 2013-12-18 | 2017-04-11 | Merck Sharp & Dohme Corp. | Thioether-piperidinyl orexin receptor antagonists |
| TW201613891A (en) | 2014-02-12 | 2016-04-16 | Eolas Therapeutics Inc | Substituted prolines / piperidines as orexin receptor antagonists |
| TW201613864A (en) | 2014-02-20 | 2016-04-16 | Takeda Pharmaceutical | Novel compounds |
| JP2017100950A (ja) | 2014-04-04 | 2017-06-08 | 大正製薬株式会社 | オキソ複素環誘導体 |
| JP2017100951A (ja) | 2014-04-04 | 2017-06-08 | 大正製薬株式会社 | オキサゾリジノン及びオキサジナノン誘導体 |
| CN105377840B (zh) | 2014-05-28 | 2017-12-22 | 杭州普晒医药科技有限公司 | 一种二氮杂环庚烷化合物的盐及其晶型与无定型物 |
| US10221170B2 (en) | 2014-08-13 | 2019-03-05 | Eolas Therapeutics, Inc. | Difluoropyrrolidines as orexin receptor modulators |
| US20160051533A1 (en) | 2014-08-20 | 2016-02-25 | Ladd Research LLC | Diagnosis and pharmacological treatment of seasonal affective disorder and symptoms of seasonality |
| GB201415569D0 (en) | 2014-09-03 | 2014-10-15 | C4X Discovery Ltd | Therapeutic Compounds |
| US10196383B2 (en) | 2015-07-17 | 2019-02-05 | Sunshine Lake Pharma Co., Ltd. | Substituted quinazoline compounds and preparation and uses thereof |
| GB201601703D0 (en) | 2016-01-29 | 2016-03-16 | C4X Discovery Ltd | Therapeutic compounds |
| US10828302B2 (en) | 2016-03-10 | 2020-11-10 | Janssen Pharmaceutica Nv | Methods of treating depression using orexin-2 receptor antagonists |
| US20210169883A1 (en) | 2018-07-27 | 2021-06-10 | Icahn School Of Medicine At Mount Sinai | Method of treating aggression with orexin receptor antagonists |
| GB201820458D0 (en) | 2018-12-14 | 2019-01-30 | Heptares Therapeutics Ltd | Ox1 antagonists |
-
2010
- 2010-10-21 EP EP10773477.4A patent/EP2491038B1/en active Active
- 2010-10-21 HU HUE16163733A patent/HUE043962T2/hu unknown
- 2010-10-21 LT LTEP16163733.5T patent/LT3093291T/lt unknown
- 2010-10-21 PL PL10773477.4T patent/PL2491038T3/pl unknown
- 2010-10-21 ME MEP-2016-135A patent/ME02437B/me unknown
- 2010-10-21 HR HRP20160781TT patent/HRP20160781T1/hr unknown
- 2010-10-21 BR BR112012010820-4A patent/BR112012010820B1/pt active IP Right Grant
- 2010-10-21 MX MX2012004753A patent/MX2012004753A/es active IP Right Grant
- 2010-10-21 PT PT16163733T patent/PT3093291T/pt unknown
- 2010-10-21 RS RS20160501A patent/RS54945B1/sr unknown
- 2010-10-21 EP EP19172579.5A patent/EP3581575A1/en active Pending
- 2010-10-21 CN CN201080058816.XA patent/CN102781942B/zh active Active
- 2010-10-21 HU HUE10773477A patent/HUE028650T2/en unknown
- 2010-10-21 WO PCT/US2010/053606 patent/WO2011050198A1/en not_active Ceased
- 2010-10-21 ME MEP-2019-199A patent/ME03452B/me unknown
- 2010-10-21 TR TR2019/10327T patent/TR201910327T4/tr unknown
- 2010-10-21 EP EP16163733.5A patent/EP3093291B1/en active Active
- 2010-10-21 US US13/503,231 patent/US8653263B2/en not_active Ceased
- 2010-10-21 JO JOP/2010/0362A patent/JO3267B1/ar active
- 2010-10-21 SI SI201031214A patent/SI2491038T1/sl unknown
- 2010-10-21 KR KR1020177034281A patent/KR101859409B1/ko active Active
- 2010-10-21 KR KR1020177034279A patent/KR101859400B1/ko active Active
- 2010-10-21 DK DK16163733.5T patent/DK3093291T3/da active
- 2010-10-21 EA EA201270591A patent/EA022766B1/ru unknown
- 2010-10-21 ES ES10773477.4T patent/ES2585806T3/es active Active
- 2010-10-21 CA CA2778484A patent/CA2778484C/en active Active
- 2010-10-21 AU AU2010310595A patent/AU2010310595B2/en active Active
- 2010-10-21 SI SI201031898T patent/SI3093291T1/sl unknown
- 2010-10-21 US US16/391,791 patent/USRE48841E1/en active Active
- 2010-10-21 KR KR1020127013101A patent/KR20120105449A/ko not_active Withdrawn
- 2010-10-21 ES ES16163733T patent/ES2735411T3/es active Active
- 2010-10-21 SM SM20190392T patent/SMT201900392T1/it unknown
- 2010-10-21 PH PH1/2012/500796A patent/PH12012500796A1/en unknown
- 2010-10-21 UA UAA201206182A patent/UA107812C2/ru unknown
- 2010-10-21 DK DK10773477.4T patent/DK2491038T3/da active
- 2010-10-21 RS RS20190878A patent/RS59004B1/sr unknown
- 2010-10-21 JP JP2012535384A patent/JP5759470B2/ja active Active
- 2010-10-21 PT PT107734774T patent/PT2491038T/pt unknown
- 2010-10-21 NZ NZ599629A patent/NZ599629A/en unknown
- 2010-10-21 PL PL16163733T patent/PL3093291T3/pl unknown
- 2010-10-22 TW TW099136022A patent/TWI481613B/zh active
- 2010-10-22 CL CL2010001162A patent/CL2010001162A1/es unknown
- 2010-10-22 PE PE2010001000A patent/PE20110404A1/es active IP Right Grant
- 2010-10-22 AR ARP100103874A patent/AR078731A1/es active IP Right Grant
- 2010-10-25 UY UY0001032966A patent/UY32966A/es active IP Right Grant
-
2012
- 2012-04-17 IL IL219234A patent/IL219234A/en active IP Right Grant
- 2012-04-20 NI NI201200062A patent/NI201200062A/es unknown
- 2012-05-11 CO CO12077916A patent/CO6541572A2/es unknown
- 2012-05-17 EC ECSP12011908 patent/ECSP12011908A/es unknown
- 2012-05-23 CR CR20120273A patent/CR20120273A/es unknown
-
2013
- 2013-12-23 US US14/138,941 patent/US9079911B2/en active Active
-
2015
- 2015-06-09 US US14/734,225 patent/US20150335651A1/en not_active Abandoned
- 2015-10-13 AU AU2015242975A patent/AU2015242975B2/en active Active
-
2016
- 2016-07-05 SM SM201600216T patent/SMT201600216B/it unknown
- 2016-07-05 CY CY20161100629T patent/CY1117743T1/el unknown
-
2017
- 2017-01-24 US US15/413,965 patent/US20170129901A1/en not_active Abandoned
-
2018
- 2018-03-14 JO JOP/2018/0019A patent/JOP20180019B1/ar active
-
2019
- 2019-03-07 AR ARP190100557A patent/AR114667A2/es unknown
- 2019-07-05 HR HRP20191220TT patent/HRP20191220T1/hr unknown
- 2019-07-26 CY CY20191100794T patent/CY1121848T1/el unknown
- 2019-10-15 US US16/601,832 patent/US11059828B2/en active Active
-
2021
- 2021-07-09 US US17/372,168 patent/US11667644B2/en active Active
-
2023
- 2023-06-02 US US18/327,990 patent/US12378254B2/en active Active
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US12378254B2 (en) | 2009-10-23 | 2025-08-05 | Janssen Pharmaceutica Nv | Disubstituted octahydropyrrolo[3,4-c]pyrroles as orexin receptor modulators |
| KR20220136475A (ko) * | 2016-03-10 | 2022-10-07 | 얀센 파마슈티카 엔.브이. | 오렉신-2 수용체 길항제를 사용한 우울증의 치료 방법 |
| US12201634B2 (en) | 2016-03-10 | 2025-01-21 | Janssen Pharmaceutica Nv | Methods of treating depression using orexin-2 receptor antagonists |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US12378254B2 (en) | Disubstituted octahydropyrrolo[3,4-c]pyrroles as orexin receptor modulators | |
| US9586962B2 (en) | Disubstituted octahydropyrrolo [3,4-C] pyrroles as orexin receptor modulators | |
| EP2491034A1 (en) | Fused heterocyclic compounds as orexin receptor modulators | |
| HK1231463B (en) | Disubstituted octahy - dropyrrolo [3,4-c]pyrroles as orexin receptor modulators | |
| HK1175463B (en) | Disubstituted octahy - dropyrrolo [3,4-c]pyrroles as orexin receptor modulators |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
Patent event date: 20120521 Patent event code: PA01051R01D Comment text: International Patent Application |
|
| PG1501 | Laying open of application | ||
| A201 | Request for examination | ||
| PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 20151019 Comment text: Request for Examination of Application |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20161214 Patent event code: PE09021S01D |
|
| E701 | Decision to grant or registration of patent right | ||
| PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 20170825 |
|
| PA0104 | Divisional application for international application |
Comment text: Divisional Application for International Patent Patent event code: PA01041R01D Patent event date: 20171127 |
|
| PC1201 | Submission of document of withdrawal after decision of registration |
Comment text: [Withdrawal of Procedure relating to Patent, etc.] Withdrawal (Abandonment) Patent event date: 20171128 Patent event code: PC12012R01D Comment text: Decision to Grant Registration Patent event date: 20170825 Patent event code: PC12011S01I |
|
| WITR | Withdrawal of patent application after decision to grant |