KR101773208B1 - 질소 함유 스피로 고리 화합물 및 이의 의약 용도 - Google Patents
질소 함유 스피로 고리 화합물 및 이의 의약 용도 Download PDFInfo
- Publication number
- KR101773208B1 KR101773208B1 KR1020127001455A KR20127001455A KR101773208B1 KR 101773208 B1 KR101773208 B1 KR 101773208B1 KR 1020127001455 A KR1020127001455 A KR 1020127001455A KR 20127001455 A KR20127001455 A KR 20127001455A KR 101773208 B1 KR101773208 B1 KR 101773208B1
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- KR
- South Korea
- Prior art keywords
- pharmaceutically acceptable
- solvate
- acceptable salt
- compound according
- mixture
- 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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- 0 *C1C(CCC2)(CN2c2c3cc[n]c3ncn2)N(*)C1 Chemical compound *C1C(CCC2)(CN2c2c3cc[n]c3ncn2)N(*)C1 0.000 description 5
- RHCVRBMRYIPJEQ-UHFFFAOYSA-N CC(C)(C)OC(N(CCC1)C1(CCC=O)C(OC)=O)=O Chemical compound CC(C)(C)OC(N(CCC1)C1(CCC=O)C(OC)=O)=O RHCVRBMRYIPJEQ-UHFFFAOYSA-N 0.000 description 2
- VUHWQBJVFDDFAF-UHFFFAOYSA-N N#CCC(N(C1)C(CCC2)(CN2c2c(cc[nH]3)c3ncn2)C1(F)F)=O Chemical compound N#CCC(N(C1)C(CCC2)(CN2c2c(cc[nH]3)c3ncn2)C1(F)F)=O VUHWQBJVFDDFAF-UHFFFAOYSA-N 0.000 description 2
- OTLJPDNWNUSUFF-UHFFFAOYSA-N N#CCC(N(CCC1)C1(CCC1)CN1c1c(cc[nH]2)c2ncn1)=O Chemical compound N#CCC(N(CCC1)C1(CCC1)CN1c1c(cc[nH]2)c2ncn1)=O OTLJPDNWNUSUFF-UHFFFAOYSA-N 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N NCc1ccccc1 Chemical compound NCc1ccccc1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- GWQBXRYSVSZLSL-UHFFFAOYSA-N O=C1OC(C(Cl)(Cl)Cl)N2C1CCC2 Chemical compound O=C1OC(C(Cl)(Cl)Cl)N2C1CCC2 GWQBXRYSVSZLSL-UHFFFAOYSA-N 0.000 description 2
- YZAJNACTNXAHDE-UHFFFAOYSA-N C=CCC1(CCC2)N2C(C(Cl)(Cl)Cl)OC1=O Chemical compound C=CCC1(CCC2)N2C(C(Cl)(Cl)Cl)OC1=O YZAJNACTNXAHDE-UHFFFAOYSA-N 0.000 description 1
- UGIJIQIALDVXGI-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CC1(C(CO)(F)F)NC(OCc1ccccc1)=O)=O Chemical compound CC(C)(C)OC(N(CC1)CC1(C(CO)(F)F)NC(OCc1ccccc1)=O)=O UGIJIQIALDVXGI-UHFFFAOYSA-N 0.000 description 1
- IAICXCUCYWQORU-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CC1(C(COS(C)(=O)=O)(F)F)NC(OCc1ccccc1)=O)=O Chemical compound CC(C)(C)OC(N(CC1)CC1(C(COS(C)(=O)=O)(F)F)NC(OCc1ccccc1)=O)=O IAICXCUCYWQORU-UHFFFAOYSA-N 0.000 description 1
- HGHASUSCASSBOZ-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CC1C(O)=O)O Chemical compound CC(C)(C)OC(N(CC1)CC1C(O)=O)O HGHASUSCASSBOZ-UHFFFAOYSA-N 0.000 description 1
- YPRYOWRNYJLPSF-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CC1C(OCC=C(F)F)=O)=O Chemical compound CC(C)(C)OC(N(CC1)CC1C(OCC=C(F)F)=O)=O YPRYOWRNYJLPSF-UHFFFAOYSA-N 0.000 description 1
- GRRMZWDKDUHUQF-UHFFFAOYSA-N CC(C)(C)OC(N(CCC1)C1(CCCNCc1ccccc1)C(OC)=O)=O Chemical compound CC(C)(C)OC(N(CCC1)C1(CCCNCc1ccccc1)C(OC)=O)=O GRRMZWDKDUHUQF-UHFFFAOYSA-N 0.000 description 1
- QTBBFQJUNQVAGJ-UHFFFAOYSA-N CC(C)(C)OC(N(CCC1)C1(CCCO)C(OC)=O)=O Chemical compound CC(C)(C)OC(N(CCC1)C1(CCCO)C(OC)=O)=O QTBBFQJUNQVAGJ-UHFFFAOYSA-N 0.000 description 1
- CEGYYJAUSJKLMA-UHFFFAOYSA-N CC(C)(C)OC(N(CCC1)CC1(CC1)N1C(OCc1ccccc1)=O)=O Chemical compound CC(C)(C)OC(N(CCC1)CC1(CC1)N1C(OCc1ccccc1)=O)=O CEGYYJAUSJKLMA-UHFFFAOYSA-N 0.000 description 1
- NXILIHONWRXHFA-UHFFFAOYSA-N CC(C)(C)OC(N(CCC1)CC1C(O)=O)=O Chemical compound CC(C)(C)OC(N(CCC1)CC1C(O)=O)=O NXILIHONWRXHFA-UHFFFAOYSA-N 0.000 description 1
- NRIMEYHRPGUDTK-AATRIKPKSA-N CC(C)(C)OC(N(CCC1)CC1C(OC/C=C/C)=O)=O Chemical compound CC(C)(C)OC(N(CCC1)CC1C(OC/C=C/C)=O)=O NRIMEYHRPGUDTK-AATRIKPKSA-N 0.000 description 1
- VLOJSBQEPMEZCA-UHFFFAOYSA-N CC(C)(C)OC(N(CCCCCCO)CCN)=O Chemical compound CC(C)(C)OC(N(CCCCCCO)CCN)=O VLOJSBQEPMEZCA-UHFFFAOYSA-N 0.000 description 1
- YAGUGWDMCPHBFF-UHFFFAOYSA-N CC(C1)C(CCC2)(CN2c2c(cc[nH]3)c3ncn2)N1C(CC#N)=O Chemical compound CC(C1)C(CCC2)(CN2c2c(cc[nH]3)c3ncn2)N1C(CC#N)=O YAGUGWDMCPHBFF-UHFFFAOYSA-N 0.000 description 1
- FDSLGXNJYBLDDV-UHFFFAOYSA-N CC(CC1)C(CCC2)(CN2c2c(cc[nH]3)c3ncn2)N1C(CC#N)=O Chemical compound CC(CC1)C(CCC2)(CN2c2c(cc[nH]3)c3ncn2)N1C(CC#N)=O FDSLGXNJYBLDDV-UHFFFAOYSA-N 0.000 description 1
- FFYXWYIFHDEHEK-UHFFFAOYSA-N CC(CCl)N(CC(OC(C)(C)C)=O)Cc1ccccc1 Chemical compound CC(CCl)N(CC(OC(C)(C)C)=O)Cc1ccccc1 FFYXWYIFHDEHEK-UHFFFAOYSA-N 0.000 description 1
- KZTZQVGKKNYHST-UHFFFAOYSA-N CC(CN(CC(OC(C)(C)C)=O)Cc1ccccc1)Cl Chemical compound CC(CN(CC(OC(C)(C)C)=O)Cc1ccccc1)Cl KZTZQVGKKNYHST-UHFFFAOYSA-N 0.000 description 1
- TXUASIWBVUPKRO-UHFFFAOYSA-N CC(CO)N(CC(OC(C)(C)C)=O)Cc1ccccc1 Chemical compound CC(CO)N(CC(OC(C)(C)C)=O)Cc1ccccc1 TXUASIWBVUPKRO-UHFFFAOYSA-N 0.000 description 1
- XYWPVZJIDYTEQP-UHFFFAOYSA-N CC1C(CCC2)(CN2c2c(cc[nH]3)c3ncn2)NC1 Chemical compound CC1C(CCC2)(CN2c2c(cc[nH]3)c3ncn2)NC1 XYWPVZJIDYTEQP-UHFFFAOYSA-N 0.000 description 1
- DDWZYWSLHBDVGR-UHFFFAOYSA-N Cc1cc(C)n[n]1C(CC#N)=O Chemical compound Cc1cc(C)n[n]1C(CC#N)=O DDWZYWSLHBDVGR-UHFFFAOYSA-N 0.000 description 1
- HFFLGKNGCAIQMO-UHFFFAOYSA-N O=CC(Cl)(Cl)Cl Chemical compound O=CC(Cl)(Cl)Cl HFFLGKNGCAIQMO-UHFFFAOYSA-N 0.000 description 1
- ONIBWKKTOPOVIA-UHFFFAOYSA-N OC(C1NCCC1)=O Chemical compound OC(C1NCCC1)=O ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
- C07D487/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
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- 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
-
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- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
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- A61K31/438—The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- 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
- C07D471/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Ophthalmology & Optometry (AREA)
- Dermatology (AREA)
- Obesity (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Emergency Medicine (AREA)
- Oncology (AREA)
- Otolaryngology (AREA)
- Endocrinology (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JPJP-P-2009-179502 | 2009-07-31 | ||
| JP2009179502 | 2009-07-31 | ||
| US27413709P | 2009-08-13 | 2009-08-13 | |
| US61/274,137 | 2009-08-13 | ||
| PCT/JP2010/062873 WO2011013785A1 (ja) | 2009-07-31 | 2010-07-30 | 含窒素スピロ環化合物及びその医薬用途 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20120051649A KR20120051649A (ko) | 2012-05-22 |
| KR101773208B1 true KR101773208B1 (ko) | 2017-08-31 |
Family
ID=43529436
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020127001455A Active KR101773208B1 (ko) | 2009-07-31 | 2010-07-30 | 질소 함유 스피로 고리 화합물 및 이의 의약 용도 |
Country Status (35)
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI466885B (zh) * | 2009-07-31 | 2015-01-01 | Japan Tobacco Inc | 含氮螺環化合物及其醫藥用途 |
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