MX2007000983A - Procesos para preparar la forma cristalina i de clorhidrato de cinacalcet. - Google Patents
Procesos para preparar la forma cristalina i de clorhidrato de cinacalcet.Info
- Publication number
- MX2007000983A MX2007000983A MX2007000983A MX2007000983A MX2007000983A MX 2007000983 A MX2007000983 A MX 2007000983A MX 2007000983 A MX2007000983 A MX 2007000983A MX 2007000983 A MX2007000983 A MX 2007000983A MX 2007000983 A MX2007000983 A MX 2007000983A
- Authority
- MX
- Mexico
- Prior art keywords
- process according
- cinacalcet hydrochloride
- hours
- crystalline form
- cinacalcet
- Prior art date
Links
- QANQWUQOEJZMLL-PKLMIRHRSA-N cinacalcet hydrochloride Chemical compound Cl.N([C@H](C)C=1C2=CC=CC=C2C=CC=1)CCCC1=CC=CC(C(F)(F)F)=C1 QANQWUQOEJZMLL-PKLMIRHRSA-N 0.000 title claims abstract description 128
- 229960000478 cinacalcet hydrochloride Drugs 0.000 title claims abstract description 127
- 238000000034 method Methods 0.000 title claims abstract description 49
- 239000013078 crystal Substances 0.000 title 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 51
- 238000001914 filtration Methods 0.000 claims description 50
- VDHAWDNDOKGFTD-MRXNPFEDSA-N cinacalcet Chemical compound N([C@H](C)C=1C2=CC=CC=C2C=CC=1)CCCC1=CC=CC(C(F)(F)F)=C1 VDHAWDNDOKGFTD-MRXNPFEDSA-N 0.000 claims description 43
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 39
- 239000000203 mixture Substances 0.000 claims description 35
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 33
- 229960003315 cinacalcet Drugs 0.000 claims description 33
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 33
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 32
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 30
- 239000002904 solvent Substances 0.000 claims description 30
- 239000000725 suspension Substances 0.000 claims description 30
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 claims description 28
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims description 28
- 239000002244 precipitate Substances 0.000 claims description 28
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 19
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 18
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 17
- 238000001035 drying Methods 0.000 claims description 14
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 13
- 239000012296 anti-solvent Substances 0.000 claims description 13
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 12
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 9
- 238000005406 washing Methods 0.000 claims description 8
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 7
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims description 7
- 239000011541 reaction mixture Substances 0.000 claims description 7
- 238000010992 reflux Methods 0.000 claims description 6
- 150000002576 ketones Chemical class 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 239000000843 powder Substances 0.000 claims description 5
- 238000002441 X-ray diffraction Methods 0.000 claims description 4
- 125000004122 cyclic group Chemical group 0.000 claims description 4
- GJRQTCIYDGXPES-UHFFFAOYSA-N iso-butyl acetate Natural products CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 claims description 4
- FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 claims description 4
- OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 claims description 4
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 3
- 239000004215 Carbon black (E152) Substances 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- JYVHOGDBFNJNMR-UHFFFAOYSA-N hexane;hydrate Chemical group O.CCCCCC JYVHOGDBFNJNMR-UHFFFAOYSA-N 0.000 claims description 2
- 229930195733 hydrocarbon Natural products 0.000 claims description 2
- 150000002430 hydrocarbons Chemical class 0.000 claims description 2
- 238000003756 stirring Methods 0.000 claims 2
- GSNUFIFRDBKVIE-UHFFFAOYSA-N DMF Natural products CC1=CC=C(C)O1 GSNUFIFRDBKVIE-UHFFFAOYSA-N 0.000 claims 1
- AHVYPIQETPWLSZ-UHFFFAOYSA-N N-methyl-pyrrolidine Natural products CN1CC=CC1 AHVYPIQETPWLSZ-UHFFFAOYSA-N 0.000 claims 1
- 230000011664 signaling Effects 0.000 claims 1
- 238000002360 preparation method Methods 0.000 abstract description 7
- 239000000047 product Substances 0.000 description 47
- 239000000243 solution Substances 0.000 description 39
- 239000002585 base Substances 0.000 description 32
- 108090000445 Parathyroid hormone Proteins 0.000 description 8
- 238000001556 precipitation Methods 0.000 description 8
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 5
- 102100036893 Parathyroid hormone Human genes 0.000 description 5
- 230000002092 calcimimetic effect Effects 0.000 description 5
- 239000011575 calcium Substances 0.000 description 5
- 229910052791 calcium Inorganic materials 0.000 description 5
- 102000013830 Calcium-Sensing Receptors Human genes 0.000 description 4
- 108010050543 Calcium-Sensing Receptors Proteins 0.000 description 4
- 238000000634 powder X-ray diffraction Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 102000003982 Parathyroid hormone Human genes 0.000 description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 239000000199 parathyroid hormone Substances 0.000 description 3
- 229960001319 parathyroid hormone Drugs 0.000 description 3
- 239000011574 phosphorus Substances 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 102000005962 receptors Human genes 0.000 description 3
- 108020003175 receptors Proteins 0.000 description 3
- 230000028327 secretion Effects 0.000 description 3
- 238000001757 thermogravimetry curve Methods 0.000 description 3
- 208000005770 Secondary Hyperparathyroidism Diseases 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 229940116949 sensipar Drugs 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- 208000010392 Bone Fractures Diseases 0.000 description 1
- 206010006002 Bone pain Diseases 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- 201000002980 Hyperparathyroidism Diseases 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- -1 amine hydrochloride Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 208000020832 chronic kidney disease Diseases 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000000502 dialysis Methods 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- 238000001938 differential scanning calorimetry curve Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000002526 effect on cardiovascular system Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 229910001410 inorganic ion Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 239000002547 new drug Substances 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 210000002990 parathyroid gland Anatomy 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 229940127557 pharmaceutical product Drugs 0.000 description 1
- 238000001144 powder X-ray diffraction data Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000002411 thermogravimetry Methods 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/82—Purification; Separation; Stabilisation; Use of additives
- C07C209/84—Purification
-
- 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
- A61P3/12—Drugs for disorders of the metabolism for electrolyte homeostasis
- A61P3/14—Drugs for disorders of the metabolism for electrolyte homeostasis for calcium homeostasis
-
- 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
- A61P5/14—Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4
-
- 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
- A61P5/14—Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4
- A61P5/16—Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4 for decreasing, blocking or antagonising the activity of the thyroid hormones
-
- 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
- A61P5/18—Drugs for disorders of the endocrine system of the parathyroid hormones
- A61P5/20—Drugs for disorders of the endocrine system of the parathyroid hormones for decreasing, blocking or antagonising the activity of PTH
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/82—Purification; Separation; Stabilisation; Use of additives
- C07C209/90—Stabilisation; Use of additives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/12—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Endocrinology (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Rheumatology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Cephalosporin Compounds (AREA)
- Catalysts (AREA)
Applications Claiming Priority (17)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US68415205P | 2005-05-23 | 2005-05-23 | |
| US69698105P | 2005-07-05 | 2005-07-05 | |
| US69711105P | 2005-07-06 | 2005-07-06 | |
| US69861305P | 2005-07-11 | 2005-07-11 | |
| US70123205P | 2005-07-20 | 2005-07-20 | |
| US70291805P | 2005-07-26 | 2005-07-26 | |
| US70691005P | 2005-08-09 | 2005-08-09 | |
| US73005005P | 2005-10-24 | 2005-10-24 | |
| US73208305P | 2005-10-31 | 2005-10-31 | |
| US73300805P | 2005-11-02 | 2005-11-02 | |
| US73466905P | 2005-11-07 | 2005-11-07 | |
| US73512605P | 2005-11-08 | 2005-11-08 | |
| US73882705P | 2005-11-21 | 2005-11-21 | |
| US74178705P | 2005-12-01 | 2005-12-01 | |
| US75091005P | 2005-12-15 | 2005-12-15 | |
| US79480406P | 2006-04-24 | 2006-04-24 | |
| PCT/US2006/020304 WO2006127933A1 (en) | 2005-05-23 | 2006-05-23 | Processes for preparing cinacalcet hydrochloride crystal form i |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2007000983A true MX2007000983A (es) | 2007-04-16 |
Family
ID=37101358
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2007000983A MX2007000983A (es) | 2005-05-23 | 2006-05-23 | Procesos para preparar la forma cristalina i de clorhidrato de cinacalcet. |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US7247751B2 (enExample) |
| EP (3) | EP1883618B1 (enExample) |
| JP (3) | JP4638491B2 (enExample) |
| KR (2) | KR20070083471A (enExample) |
| CN (1) | CN101180261A (enExample) |
| AT (1) | ATE445587T1 (enExample) |
| CA (2) | CA2606099A1 (enExample) |
| ES (1) | ES2334260T3 (enExample) |
| IL (2) | IL185108A0 (enExample) |
| MX (1) | MX2007000983A (enExample) |
| TW (1) | TW200716512A (enExample) |
| WO (2) | WO2006127933A1 (enExample) |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2008012061A (es) * | 2006-03-23 | 2008-12-17 | Amgen Inc | Metodos y composiciones para elaborar y utilizar polimorfos de cinacalcet. |
| WO2008000423A1 (en) * | 2006-06-27 | 2008-01-03 | Sandoz Ag | Crystalline form of cinacalcet |
| WO2008000422A1 (en) * | 2006-06-27 | 2008-01-03 | Sandoz Ag | Amorphous form of cinacalcet |
| EP1913941A1 (en) * | 2006-10-19 | 2008-04-23 | Sandoz AG | Polymorphic forms and solvates of Cinacalcet hydrochloride |
| WO2008027522A2 (en) * | 2006-09-01 | 2008-03-06 | Teva Pharmaceutical Industries Ltd. | Solid composites of a calicum receptor-active compound |
| WO2008058236A2 (en) * | 2006-11-08 | 2008-05-15 | Dr. Reddy's Labortories, Ltd. | Methods for preparing cinacalcet hydrochloride |
| WO2008063645A1 (en) * | 2006-11-20 | 2008-05-29 | Teva Pharmaceutical Industries Ltd. | Process for preparing cinacalcet |
| ES2569483T3 (es) * | 2007-06-21 | 2016-05-11 | Amgen Inc. | Métodos para sintetizar cinacalcet y sales del mismo |
| ITMI20071261A1 (it) | 2007-06-22 | 2008-12-23 | Dipharma Francis Srl | Procedimento per la preparazione di cinacalcet |
| US20090093652A1 (en) * | 2007-08-16 | 2009-04-09 | Michal Rafilovich | Crystalline forms cinacalcet fumarate and cinacalcet succinate and processes for preparation thereof |
| US8350086B2 (en) | 2007-09-18 | 2013-01-08 | Medichem, S.A. | Process for preparing cinacalcet hydrochloride |
| EP2197273B1 (en) * | 2007-10-01 | 2014-09-24 | Ascenta Therapeutics, Inc. | Process for preparing r-gossypol l-phenylalaninol dienamine |
| EP2300415A2 (en) * | 2008-05-05 | 2011-03-30 | Medichem, S.A. | Process for controlling the particle size of a 3-(trifluoromethyl)phenyl¨-1-aminopropane derivative |
| EP2321256B1 (en) * | 2008-06-18 | 2014-11-12 | ERREGIERRE S.p.A. | Process for the synthesis of cinacalcet hydrochloride |
| US20110178326A1 (en) * | 2008-08-06 | 2011-07-21 | Actavis Group Ptc Ehf | Unsaturated cinacalcet salts and processes for preparing cinacalcet hydrochloride |
| WO2010067204A1 (en) | 2008-12-08 | 2010-06-17 | Actavis Group Ptc Ehf | Highly pure cinacalcet or a pharmaceutically acceptable salt thereof |
| AU2010215520B2 (en) | 2009-02-19 | 2016-07-21 | F.I.S. - Fabbrica Italiana Sintetici S.P.A. | Process for preparing Cinacalcet hydrochloride |
| NZ595023A (en) | 2009-03-05 | 2013-09-27 | Cipla Ltd | Process for the preparation of cinacalcet and salts thereof, and intermediates for use in the process |
| WO2010128388A2 (en) | 2009-05-08 | 2010-11-11 | Aurobindo Pharma Limited | An improved process for the preparation of intermediate compounds useful for the preparation of cinacalcet |
| ES2445532T3 (es) | 2009-09-10 | 2014-03-03 | Zach System S.P.A. | Proceso para preparar cinacalcet |
| US8722732B2 (en) | 2009-09-29 | 2014-05-13 | Nektar Therapeutics | Oligomer-calcimimetic conjugates and related compounds |
| IT1396623B1 (it) | 2009-11-26 | 2012-12-14 | Dipharma Francis Srl | Procedimento per la preparazione di cinacalcet e suoi intermedi |
| CZ2011770A3 (cs) * | 2011-11-25 | 2013-01-16 | Zentiva, K.S. | Zpusob výroby Cinacalcetu |
| CN103450027B (zh) | 2012-05-29 | 2015-07-29 | 上海京新生物医药有限公司 | 盐酸西那卡塞的制备方法 |
| FR2995307A1 (fr) | 2012-09-07 | 2014-03-14 | Prod Chim Auxiliaires Et De Synthese | Procede de preparation du cinacalcet et de ses sels pharmaceutiquement acceptables |
| CN103739500B (zh) * | 2012-12-27 | 2016-03-23 | 国药一心制药有限公司 | 一种盐酸西那卡塞的合成与精制方法 |
| CN103193655B (zh) * | 2013-04-15 | 2015-06-24 | 山东新华制药股份有限公司 | 盐酸西那卡塞晶型ⅰ的制备方法 |
| CN104512864B (zh) * | 2013-09-30 | 2017-08-22 | 中国石油化工股份有限公司 | 一种低温脱除微量碳氧化物的方法 |
| TWI665190B (zh) | 2013-11-15 | 2019-07-11 | 阿克比治療有限公司 | ｛［５－（３－氯苯基）－３－羥基吡啶－２－羰基］胺基｝乙酸之固體型式，其組合物及用途 |
| BR102015025502B1 (pt) * | 2015-04-30 | 2022-06-21 | Aegerion Pharmaceuticals, Inc | Composição de lomitapida, tablete, produto de lomitapida, métodos para analisar uma composição de amostra de lomitapida e para determinar uma quantidade de uma impureza em uma amostra da composição |
| CN104892428A (zh) * | 2015-06-05 | 2015-09-09 | 南京辰逸生物科技有限公司 | 一种盐酸西那卡塞的制备方法 |
| CN106610404B (zh) * | 2015-10-21 | 2019-01-15 | 华仁药业股份有限公司 | 采用hplc法检测盐酸西那卡塞同分异构体的方法 |
| CN105439818B (zh) * | 2015-12-31 | 2017-11-28 | 苏州汇和药业有限公司 | 一种西那卡塞中间体3‑(3‑三氟甲基苯基)丙醇的合成方法 |
| CN107879939A (zh) * | 2016-09-30 | 2018-04-06 | 上海天慈生物谷生物工程有限公司 | 一种制备 n‑((1r)‑1‑(1‑萘基)乙基)‑3‑(3‑(三氟甲基)苯基)丙‑1‑胺盐酸盐的方法 |
| KR20200022712A (ko) | 2018-08-23 | 2020-03-04 | 주식회사 오스코텍 | 8-브로모-2-(1-메틸피페리딘-4-일아미노)-4-(4-페녹시페닐아미노)피리도[4,3-d]피리미딘-5(6H)-온 염산염의 결정다형체 및 그 제조방법 |
| CN109096119B (zh) * | 2018-10-29 | 2019-10-25 | 江苏永安制药有限公司 | 一种制备盐酸西那卡塞的方法 |
| CN110041206B (zh) * | 2019-04-29 | 2021-10-19 | 梯尔希（南京）药物研发有限公司 | 一种西那卡塞杂质的制备方法 |
| CN111153832B (zh) * | 2020-01-20 | 2022-02-25 | 广州九植医药科技有限公司 | 一种西那卡塞杂质的制备方法 |
| JP2026522454A (ja) * | 2023-06-30 | 2026-07-07 | チョン クン ダン ファーマシューティカル コーポレーション | 化合物の新規な製造方法および新規な結晶形 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4966988A (en) | 1989-02-17 | 1990-10-30 | Chevron Research Company | Process for preparing acetonitrile 3-trifluoromethyl benzene |
| US6011068A (en) | 1991-08-23 | 2000-01-04 | Nps Pharmaceuticals, Inc. | Calcium receptor-active molecules |
| US6031003A (en) | 1991-08-23 | 2000-02-29 | Nps Pharmaceuticals, Inc. | Calcium receptor-active molecules |
| US6313146B1 (en) | 1991-08-23 | 2001-11-06 | Nps Pharmaceuticals, Inc. | Calcium receptor-active molecules |
| EP1275635A1 (en) | 1994-10-21 | 2003-01-15 | Nps Pharmaceuticals, Inc. | Calcium receptor-active compounds |
| US5648541A (en) * | 1995-09-28 | 1997-07-15 | Nps Pharmaceuticals, Inc. | Chiral reductions of imines leading to the syntheses of optically active amines |
| JP4117506B2 (ja) * | 1996-05-01 | 2008-07-16 | エヌピーエス ファーマシューティカルズ インコーポレイテッド | 無機イオン活性化合物 |
| GB9812413D0 (en) | 1998-06-10 | 1998-08-05 | Glaxo Group Ltd | Compound and its use |
| AR045637A1 (es) * | 2003-09-12 | 2005-11-02 | Amgen Inc | Formulacion de disolucion rapida de un compuesto activo frente a los receptores de calcio |
-
2006
- 2006-05-23 EP EP06771215A patent/EP1883618B1/en not_active Expired - Lifetime
- 2006-05-23 JP JP2007522852A patent/JP4638491B2/ja not_active Expired - Fee Related
- 2006-05-23 CA CA002606099A patent/CA2606099A1/en not_active Abandoned
- 2006-05-23 US US11/439,570 patent/US7247751B2/en not_active Expired - Fee Related
- 2006-05-23 TW TW095118275A patent/TW200716512A/zh unknown
- 2006-05-23 EP EP06771214A patent/EP1805135A2/en not_active Withdrawn
- 2006-05-23 KR KR1020077001966A patent/KR20070083471A/ko not_active Ceased
- 2006-05-23 KR KR1020077004036A patent/KR20070088485A/ko not_active Ceased
- 2006-05-23 JP JP2007522851A patent/JP2008507565A/ja active Pending
- 2006-05-23 CA CA002605736A patent/CA2605736A1/en not_active Abandoned
- 2006-05-23 ES ES06771215T patent/ES2334260T3/es not_active Expired - Lifetime
- 2006-05-23 MX MX2007000983A patent/MX2007000983A/es not_active Application Discontinuation
- 2006-05-23 EP EP08012814A patent/EP1975150A1/en not_active Withdrawn
- 2006-05-23 CN CNA2006800179392A patent/CN101180261A/zh active Pending
- 2006-05-23 WO PCT/US2006/020304 patent/WO2006127933A1/en not_active Ceased
- 2006-05-23 AT AT06771215T patent/ATE445587T1/de not_active IP Right Cessation
- 2006-05-23 WO PCT/US2006/020303 patent/WO2006127932A2/en not_active Ceased
- 2006-05-23 US US11/440,246 patent/US7294735B2/en not_active Expired - Fee Related
-
2007
- 2007-08-07 IL IL185108A patent/IL185108A0/en unknown
- 2007-08-23 IL IL185494A patent/IL185494A0/en unknown
-
2010
- 2010-09-02 JP JP2010197123A patent/JP2010280715A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| US20070099998A1 (en) | 2007-05-03 |
| JP2008507565A (ja) | 2008-03-13 |
| EP1975150A1 (en) | 2008-10-01 |
| US7247751B2 (en) | 2007-07-24 |
| EP1883618A1 (en) | 2008-02-06 |
| CN101180261A (zh) | 2008-05-14 |
| TW200716512A (en) | 2007-05-01 |
| US20070060645A1 (en) | 2007-03-15 |
| CA2606099A1 (en) | 2006-11-30 |
| WO2006127933A1 (en) | 2006-11-30 |
| KR20070083471A (ko) | 2007-08-24 |
| IL185108A0 (en) | 2007-12-03 |
| EP1883618B1 (en) | 2009-10-14 |
| US7294735B2 (en) | 2007-11-13 |
| WO2006127933A8 (en) | 2007-08-30 |
| KR20070088485A (ko) | 2007-08-29 |
| JP2008507566A (ja) | 2008-03-13 |
| CA2605736A1 (en) | 2006-11-30 |
| JP2010280715A (ja) | 2010-12-16 |
| ES2334260T3 (es) | 2010-03-08 |
| ATE445587T1 (de) | 2009-10-15 |
| EP1805135A2 (en) | 2007-07-11 |
| WO2006127932A2 (en) | 2006-11-30 |
| IL185494A0 (en) | 2008-01-06 |
| WO2006127932A3 (en) | 2007-02-01 |
| JP4638491B2 (ja) | 2011-02-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US7247751B2 (en) | Processes for preparing cinacalcet hydrochloride crystal Form I | |
| JP2008507566A6 (ja) | シナカルセト塩酸塩結晶フォームｉの調製方法 | |
| AU2014239995B2 (en) | Salt of omecamtiv mecarbil and process for preparing salt | |
| CN101573350B (zh) | 甲磺酸伊马替尼的多晶型及其制备方法以及无定形和α型的甲磺酸伊马替尼 | |
| JP2014530805A (ja) | アジルサルタンの結晶形並びにその製造及び使用 | |
| IL194329A (en) | Crystalline form of tigecycline ii and its processes | |
| JP2008546719A (ja) | 結晶形のｏ−デスメチルベンラファキシン | |
| WO2009017813A1 (en) | O-desmethyl venlafaxine saccharinate | |
| US20090093652A1 (en) | Crystalline forms cinacalcet fumarate and cinacalcet succinate and processes for preparation thereof | |
| EP1305303A1 (en) | NOVEL FORM OF (R)- i N /i - 5-METHYL-8-(4-METHYLPIPERAZIN-1-YL)-1,2,3,4-TETRAHYDRO-2-NAPHTHYL]-4-MORPHOLINOBENZAMIDE | |
| AU2001272872A1 (en) | Novel form of (R)-N-(5-methyl-8-(4-methylpiperazin-1-YL)-1,2,3,4-tetrahydro -2-naphthyl)-4-morpholinobenzamide | |
| WO2018010622A1 (zh) | 化合物的晶型及其制备方法、组合物和应用 | |
| CA3213234A1 (en) | Preparation method of quinoline derivative compounds | |
| JP6818031B2 (ja) | モルホリン誘導体の塩、結晶形、その製造方法、これらを含む医薬組成物およびその用途 | |
| CN110914246A (zh) | 3-(3,5-二氯-4-羟基苯甲酰)-1,1-二氧代-2,3-二氢-1,3-苯并噻唑的晶型及其盐 | |
| AU2016236659B9 (en) | AHU377 crystal form, preparation method and use thereof | |
| JP5968881B2 (ja) | カルシウム模倣化合物の新規多形 | |
| EP2658840A1 (en) | Process for making fingolimod hydrochloride crystals | |
| JPH09124644A (ja) | テラゾシン結晶性ポリモルフ及びその製薬組成物 | |
| CN110606826A (zh) | 托拉塞米钠一水合物、其晶型及组合物 | |
| WO2011029460A1 (en) | Nonhygroscopic linezolid salts | |
| CN114845993A (zh) | 1-(4-苄氧基-苄基)-3-甲基-硫脲的多晶型物 | |
| US20120220663A1 (en) | Solid forms of aliskiren hemifumarate and processes for preparation thereof | |
| KR100857342B1 (ko) | 시부트라민의 신규한 유기산염 및 그의 제조방법 | |
| WO2013064427A1 (en) | A process for making crystalline delta-form of ivabradine hydrochloride |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal |