OA12917A - Novel Polymorph of N-Methyl-N-(3-{3-[2-Thienylcarbonyl]-Pyrazol-[1,5-alpha]-Pyrimidin-7-YL}Pheny) Acetamide and Compositions and Methods Related thereto. - Google Patents
Novel Polymorph of N-Methyl-N-(3-{3-[2-Thienylcarbonyl]-Pyrazol-[1,5-alpha]-Pyrimidin-7-YL}Pheny) Acetamide and Compositions and Methods Related thereto. Download PDFInfo
- Publication number
- OA12917A OA12917A OA1200500060A OA1200500060A OA12917A OA 12917 A OA12917 A OA 12917A OA 1200500060 A OA1200500060 A OA 1200500060A OA 1200500060 A OA1200500060 A OA 1200500060A OA 12917 A OA12917 A OA 12917A
- Authority
- OA
- OAPI
- Prior art keywords
- composition
- polymorph form
- weight
- compound
- polymorph
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 98
- 238000000034 method Methods 0.000 title claims abstract description 24
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 title 2
- 208000013738 Sleep Initiation and Maintenance disease Diseases 0.000 claims abstract description 14
- 206010022437 insomnia Diseases 0.000 claims abstract description 13
- 229940125904 compound 1 Drugs 0.000 claims description 58
- 239000013078 crystal Substances 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- 239000002002 slurry Substances 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 9
- 239000002775 capsule Substances 0.000 claims description 6
- 239000006187 pill Substances 0.000 claims description 5
- 239000003826 tablet Substances 0.000 claims description 5
- 239000012535 impurity Substances 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- 230000000147 hypnotic effect Effects 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 3
- 238000002329 infrared spectrum Methods 0.000 claims description 2
- 210000002027 skeletal muscle Anatomy 0.000 claims description 2
- SGPGESCZOCHFCL-UHFFFAOYSA-N Tilisolol hydrochloride Chemical compound [Cl-].C1=CC=C2C(=O)N(C)C=C(OCC(O)C[NH2+]C(C)(C)C)C2=C1 SGPGESCZOCHFCL-UHFFFAOYSA-N 0.000 claims 10
- 206010021118 Hypotonia Diseases 0.000 claims 1
- 208000018127 Idiopathic intracranial hypertension Diseases 0.000 claims 1
- 238000002441 X-ray diffraction Methods 0.000 claims 1
- 239000002552 dosage form Substances 0.000 claims 1
- 230000001939 inductive effect Effects 0.000 claims 1
- 230000036640 muscle relaxation Effects 0.000 claims 1
- 208000001381 pseudotumor cerebri Diseases 0.000 claims 1
- 230000001773 anti-convulsant effect Effects 0.000 abstract description 2
- 239000001961 anticonvulsive agent Substances 0.000 abstract description 2
- 229960003965 antiepileptics Drugs 0.000 abstract description 2
- 239000002249 anxiolytic agent Substances 0.000 abstract description 2
- 230000000949 anxiolytic effect Effects 0.000 abstract description 2
- 230000004799 sedative–hypnotic effect Effects 0.000 abstract 1
- 229940125706 skeletal muscle relaxant agent Drugs 0.000 abstract 1
- 239000002904 solvent Substances 0.000 description 38
- 238000002425 crystallisation Methods 0.000 description 27
- 230000008025 crystallization Effects 0.000 description 26
- 239000000243 solution Substances 0.000 description 22
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 21
- 239000006184 cosolvent Substances 0.000 description 12
- 239000007787 solid Substances 0.000 description 12
- 125000004429 atom Chemical group 0.000 description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
- AICOOMRHRUFYCM-ZRRPKQBOSA-N oxazine, 1 Chemical compound C([C@@H]1[C@H](C(C[C@]2(C)[C@@H]([C@H](C)N(C)C)[C@H](O)C[C@]21C)=O)CC1=CC2)C[C@H]1[C@@]1(C)[C@H]2N=C(C(C)C)OC1 AICOOMRHRUFYCM-ZRRPKQBOSA-N 0.000 description 8
- 239000008194 pharmaceutical composition Substances 0.000 description 8
- 238000000634 powder X-ray diffraction Methods 0.000 description 8
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 7
- 239000000126 substance Substances 0.000 description 6
- 229940125717 barbiturate Drugs 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 4
- 239000003326 hypnotic agent Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 238000001228 spectrum Methods 0.000 description 4
- SVUOLADPCWQTTE-UHFFFAOYSA-N 1h-1,2-benzodiazepine Chemical class N1N=CC=CC2=CC=CC=C12 SVUOLADPCWQTTE-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000003937 drug carrier Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000002667 nucleating agent Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- 229910000530 Gallium indium arsenide Inorganic materials 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- KXNLCSXBJCPWGL-UHFFFAOYSA-N [Ga].[As].[In] Chemical compound [Ga].[As].[In] KXNLCSXBJCPWGL-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000006399 behavior Effects 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 239000003874 central nervous system depressant Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000010899 nucleation Methods 0.000 description 2
- 230000003595 spectral effect Effects 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000007910 systemic administration Methods 0.000 description 2
- -1 éthanol Chemical compound 0.000 description 2
- XWSCOGPKWVNQSV-UHFFFAOYSA-N 5-bromo-2,3-dichloropyridine Chemical compound ClC1=CC(Br)=CN=C1Cl XWSCOGPKWVNQSV-UHFFFAOYSA-N 0.000 description 1
- 208000019901 Anxiety disease Diseases 0.000 description 1
- 241000557626 Corvus corax Species 0.000 description 1
- GSNUFIFRDBKVIE-UHFFFAOYSA-N DMF Natural products CC1=CC=C(C)O1 GSNUFIFRDBKVIE-UHFFFAOYSA-N 0.000 description 1
- 206010012289 Dementia Diseases 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 238000005079 FT-Raman Methods 0.000 description 1
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
- 206010019133 Hangover Diseases 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical class CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- 206010024264 Lethargy Diseases 0.000 description 1
- 229910017502 Nd:YVO4 Inorganic materials 0.000 description 1
- 238000001069 Raman spectroscopy Methods 0.000 description 1
- 208000034189 Sclerosis Diseases 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 229940094070 ambien Drugs 0.000 description 1
- 238000004164 analytical calibration Methods 0.000 description 1
- 230000000496 anti-anoxic effect Effects 0.000 description 1
- 230000003542 behavioural effect Effects 0.000 description 1
- 125000003310 benzodiazepinyl group Chemical class N1N=C(C=CC2=C1C=CC=C2)* 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 230000001914 calming effect Effects 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- OGEBRHQLRGFBNV-RZDIXWSQSA-N chembl2036808 Chemical compound C12=NC(NCCCC)=NC=C2C(C=2C=CC(F)=CC=2)=NN1C[C@H]1CC[C@H](N)CC1 OGEBRHQLRGFBNV-RZDIXWSQSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 238000013270 controlled release Methods 0.000 description 1
- 238000013480 data collection Methods 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000001037 epileptic effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000005554 hypnotics and sedatives Substances 0.000 description 1
- 125000004857 imidazopyridinyl group Chemical group N1C(=NC2=C1C=CC=N2)* 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000036651 mood Effects 0.000 description 1
- 239000003158 myorelaxant agent Substances 0.000 description 1
- 210000000653 nervous system Anatomy 0.000 description 1
- 230000000926 neurological effect Effects 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000003586 protic polar solvent Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000004467 single crystal X-ray diffraction Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229940061368 sonata Drugs 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 238000001757 thermogravimetry curve Methods 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 230000008733 trauma Effects 0.000 description 1
- 238000003828 vacuum filtration Methods 0.000 description 1
- 238000002424 x-ray crystallography Methods 0.000 description 1
- 229960004010 zaleplon Drugs 0.000 description 1
- HUNXMJYCHXQEGX-UHFFFAOYSA-N zaleplon Chemical compound CCN(C(C)=O)C1=CC=CC(C=2N3N=CC(=C3N=CC=2)C#N)=C1 HUNXMJYCHXQEGX-UHFFFAOYSA-N 0.000 description 1
- ZAFYATHCZYHLPB-UHFFFAOYSA-N zolpidem Chemical compound N1=C2C=CC(C)=CN2C(CC(=O)N(C)C)=C1C1=CC=C(C)C=C1 ZAFYATHCZYHLPB-UHFFFAOYSA-N 0.000 description 1
- 229960005111 zolpidem tartrate Drugs 0.000 description 1
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
- A61K31/495—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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
- A61P21/02—Muscle relaxants, e.g. for tetanus or cramps
-
- 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
- A61P25/20—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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Neurology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pain & Pain Management (AREA)
- Physical Education & Sports Medicine (AREA)
- Anesthesiology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US40607202P | 2002-08-26 | 2002-08-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| OA12917A true OA12917A (en) | 2006-10-13 |
Family
ID=31946959
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| OA1200500060A OA12917A (en) | 2002-08-26 | 2003-08-26 | Novel Polymorph of N-Methyl-N-(3-{3-[2-Thienylcarbonyl]-Pyrazol-[1,5-alpha]-Pyrimidin-7-YL}Pheny) Acetamide and Compositions and Methods Related thereto. |
Country Status (32)
| Country | Link |
|---|---|
| US (2) | US6903106B2 (es) |
| EP (1) | EP1532152B1 (es) |
| JP (2) | JP4522859B2 (es) |
| KR (1) | KR101063033B1 (es) |
| CN (1) | CN1319974C (es) |
| AP (1) | AP2005003220A0 (es) |
| AR (1) | AR044191A1 (es) |
| AT (1) | ATE343581T1 (es) |
| AU (1) | AU2003268212B2 (es) |
| BR (1) | BR0313695A (es) |
| CA (1) | CA2493359C (es) |
| DE (1) | DE60309332T2 (es) |
| DK (1) | DK1532152T3 (es) |
| EA (1) | EA200500421A1 (es) |
| EC (1) | ECSP055703A (es) |
| ES (1) | ES2274260T3 (es) |
| HK (1) | HK1071373A1 (es) |
| HR (1) | HRP20050288A2 (es) |
| IL (2) | IL166621A0 (es) |
| IS (1) | IS7769A (es) |
| MA (1) | MA27519A1 (es) |
| MX (1) | MXPA05002251A (es) |
| NO (1) | NO20050615L (es) |
| NZ (1) | NZ538027A (es) |
| OA (1) | OA12917A (es) |
| PE (1) | PE20040979A1 (es) |
| PL (1) | PL374436A1 (es) |
| PT (1) | PT1532152E (es) |
| TN (1) | TNSN05058A1 (es) |
| TW (1) | TWI288135B (es) |
| WO (1) | WO2004018476A1 (es) |
| ZA (1) | ZA200501125B (es) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2003268212B2 (en) * | 2002-08-26 | 2008-08-14 | Neurocrine Biosciences, Inc. | Novel polymorph of N-methyl-N-(3-{3-[2-thienylcarbonyl]-pyrazol-[1,5-alpha]-pyrimidin-7-YL}phenyl)acetamide and compositions and methods related thereto |
| US7429596B2 (en) * | 2003-06-20 | 2008-09-30 | The Regents Of The University Of California | 1H-pyrrolo [2,3-D] pyrimidine derivatives and methods of use thereof |
| WO2006044903A1 (en) * | 2004-10-18 | 2006-04-27 | Neurocrine Biosciences, Inc. | HYDRATE OF N-METHYL-N-(3-{3-[2-THIENYLCARBONYL]-PYRAZOL-[1,5-α]- PYRAMIDIN-7-YL}PHENYL)ACETAMIDE AND PROCESSES AND METHODS RELATED THERETO |
| CN100528875C (zh) * | 2005-02-18 | 2009-08-19 | 美德（江西）生物科技有限公司 | 无结晶型态的印地普隆及其制备方法 |
| EP1956021A1 (en) * | 2006-10-11 | 2008-08-13 | Ferrer Internacional, S.A. | Process for the manufacture of a crystalline pyrazolo[1,5-a]pyrimidine compound |
| EP1918290A1 (en) | 2006-10-11 | 2008-05-07 | Ferrer Internacional, S.A. | Polymorph B of N-{2-Fluoro-5-[3-(thiophene-2-carbonyl)-pyrazolo[1,5-a] pyrimidin-7-yl]-phenyl}-N-methyl-acetamide |
| CN102180879B (zh) * | 2006-11-09 | 2013-05-01 | 中国人民解放军军事医学科学院放射与辐射医学研究所 | 一种催眠药的多晶型α的乙酸溶剂化物 |
| CN101177427B (zh) * | 2006-11-09 | 2011-07-20 | 中国人民解放军军事医学科学院放射与辐射医学研究所 | 一种用于催眠的化合物的多晶型α和溶剂化物,其制备方法及含该物质的组合物 |
| WO2011118851A1 (en) | 2010-03-25 | 2011-09-29 | Yazaki Corporation | Joint Connector and Method for Identifying Bus Bar Pattern in Joint Connector |
| PT2377830T (pt) * | 2010-04-16 | 2016-07-18 | Ivoclar Vivadent Ag | Vidro cerâmico de silicato de lítio e vidro de silicato de lítio, contendo óxido de metal de transição |
| US8752545B2 (en) | 2011-02-11 | 2014-06-17 | Batmark Limited | Inhaler component |
| AT510837B1 (de) | 2011-07-27 | 2012-07-15 | Helmut Dr Buchberger | Inhalatorkomponente |
| CN102174048B (zh) * | 2011-03-08 | 2014-09-17 | 中国人民解放军军事医学科学院放射与辐射医学研究所 | 一种催眠药的新多晶型β |
| EP2753202B1 (en) | 2011-09-06 | 2016-04-27 | British American Tobacco (Investments) Ltd | Heating smokeable material |
| GB201207039D0 (en) | 2012-04-23 | 2012-06-06 | British American Tobacco Co | Heating smokeable material |
| GB2533135B (en) | 2014-12-11 | 2020-11-11 | Nicoventures Holdings Ltd | Aerosol provision systems |
| GB201511349D0 (en) | 2015-06-29 | 2015-08-12 | Nicoventures Holdings Ltd | Electronic aerosol provision systems |
| US11924930B2 (en) | 2015-08-31 | 2024-03-05 | Nicoventures Trading Limited | Article for use with apparatus for heating smokable material |
| US20170055584A1 (en) | 2015-08-31 | 2017-03-02 | British American Tobacco (Investments) Limited | Article for use with apparatus for heating smokable material |
| CA3103090C (en) | 2016-04-27 | 2023-03-28 | Nicoventures Trading Limited | Electronic aerosol provision system and vaporizer therefor |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6472528B1 (en) | 1999-08-10 | 2002-10-29 | Neurocrine Biosciences, Inc. | Synthesis of substituted pyrazolopyrimidines |
| US6399621B1 (en) | 1999-08-10 | 2002-06-04 | American Cyanamid Company | N-methyl-N-(3-{3-[2-thienylcarbonyl]-pyrazol-[1, 5-α]-pyrimidin-7-yl}phenyl)acetamide and compositions and methods related thereto |
| US6485746B1 (en) | 2000-08-25 | 2002-11-26 | Neurocrine Biosciences, Inc. | Controlled-release sedative-hypnotic compositions and methods related thereto |
| HUP0202698A3 (en) * | 1999-09-02 | 2004-12-28 | Neurocrine Biosciences Inc | Polymorphs of n-methyl-n-(3-{3-[2-thienylcarbonyl]-pyrazol-[1,5-alpha]-pyrimidin-7-yl}phenyl)acetamide and compositions and methods related thereto |
| US6384221B1 (en) * | 1999-09-02 | 2002-05-07 | Neurocrine Biosciences, Inc. | Polymorphs of N-methyl-N-(3-{3-[2-thienylcarbonyl]-pyrazol-[1,5-α]-pyrimidin-7-yl}phenyl)acetamide and compositions and methods related thereto |
| JP2001177971A (ja) * | 1999-12-20 | 2001-06-29 | Auto Network Gijutsu Kenkyusho:Kk | 回転接続装置 |
| AU2003268212B2 (en) * | 2002-08-26 | 2008-08-14 | Neurocrine Biosciences, Inc. | Novel polymorph of N-methyl-N-(3-{3-[2-thienylcarbonyl]-pyrazol-[1,5-alpha]-pyrimidin-7-YL}phenyl)acetamide and compositions and methods related thereto |
-
2003
- 2003-08-26 AU AU2003268212A patent/AU2003268212B2/en not_active Ceased
- 2003-08-26 DE DE60309332T patent/DE60309332T2/de not_active Expired - Lifetime
- 2003-08-26 TW TW092123478A patent/TWI288135B/zh not_active IP Right Cessation
- 2003-08-26 OA OA1200500060A patent/OA12917A/en unknown
- 2003-08-26 CN CNB03820245XA patent/CN1319974C/zh not_active Expired - Fee Related
- 2003-08-26 US US10/648,812 patent/US6903106B2/en not_active Expired - Lifetime
- 2003-08-26 PL PL03374436A patent/PL374436A1/xx not_active Application Discontinuation
- 2003-08-26 PE PE2003000867A patent/PE20040979A1/es not_active Application Discontinuation
- 2003-08-26 DK DK03749163T patent/DK1532152T3/da active
- 2003-08-26 MX MXPA05002251A patent/MXPA05002251A/es active IP Right Grant
- 2003-08-26 AT AT03749163T patent/ATE343581T1/de active
- 2003-08-26 PT PT03749163T patent/PT1532152E/pt unknown
- 2003-08-26 ES ES03749163T patent/ES2274260T3/es not_active Expired - Lifetime
- 2003-08-26 BR BR0313695-7A patent/BR0313695A/pt not_active Application Discontinuation
- 2003-08-26 JP JP2004531248A patent/JP4522859B2/ja not_active Expired - Fee Related
- 2003-08-26 EP EP03749163A patent/EP1532152B1/en not_active Expired - Lifetime
- 2003-08-26 WO PCT/US2003/026870 patent/WO2004018476A1/en active IP Right Grant
- 2003-08-26 CA CA002493359A patent/CA2493359C/en not_active Expired - Lifetime
- 2003-08-26 NZ NZ538027A patent/NZ538027A/en not_active IP Right Cessation
- 2003-08-26 IL IL16662103A patent/IL166621A0/xx unknown
- 2003-08-26 AP AP2005003220A patent/AP2005003220A0/xx unknown
- 2003-08-26 EA EA200500421A patent/EA200500421A1/ru unknown
- 2003-08-26 KR KR1020057003193A patent/KR101063033B1/ko active IP Right Grant
- 2003-08-27 AR ARP030103086A patent/AR044191A1/es not_active Application Discontinuation
-
2004
- 2004-12-15 US US11/013,308 patent/US7459458B2/en not_active Expired - Lifetime
-
2005
- 2005-02-01 IL IL166621A patent/IL166621A/en active IP Right Review Request
- 2005-02-03 NO NO20050615A patent/NO20050615L/no not_active Application Discontinuation
- 2005-02-08 ZA ZA200501125A patent/ZA200501125B/en unknown
- 2005-02-25 MA MA28122A patent/MA27519A1/fr unknown
- 2005-02-25 TN TNP2005000058A patent/TNSN05058A1/en unknown
- 2005-03-23 IS IS7769A patent/IS7769A/is unknown
- 2005-03-23 EC EC2005005703A patent/ECSP055703A/es unknown
- 2005-03-24 HR HR20050288A patent/HRP20050288A2/xx not_active Application Discontinuation
- 2005-05-26 HK HK05104433A patent/HK1071373A1/xx not_active IP Right Cessation
-
2009
- 2009-12-22 JP JP2009291164A patent/JP2010070561A/ja not_active Withdrawn
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ZA200501125B (en) | Novel polymorph of N-methyl-N(3-ä3-Ä2-theinylcarbonylÜ-pyrazol-Ä1,5-alphaÜ-pyrimidin-7-ylüphenyl)acetamine and compositions and methods related thereto | |
| US20060025427A1 (en) | Polymorphs of N-methyl-N-(3-{3-[2-thienylcarbonyl]-pyrazol-[1,5-alpha]-pyrimidin-7-yl}phenyl)acetamide and compositions and methods related thereto | |
| JP4592241B2 (ja) | Ｎ−メチル−Ｎ−（３−｛３−［２−チエニルカルボニル］−ピラゾール−［１，５−α］−ピリミジン−７−イル｝フェニル）アセトアミドの多形相ならびにそれに関連する組成物および方法 | |
| US7304069B2 (en) | Hydrate of N-methyl-N-(3-{3-[2-thienylcarbonyl]-pyrazol-[1,5α]-pyrimidin-7-yl}phenyl)acetamide and processes and methods related thereto | |
| JP4845139B2 (ja) | エナンチオマー的に純粋なヘキサヒドロピロロシクロペンタピリジン誘導体 |