CA2538906C - Process for preparing 4-(4-aminophenyl)-3-morpholinone - Google Patents
Process for preparing 4-(4-aminophenyl)-3-morpholinone Download PDFInfo
- Publication number
- CA2538906C CA2538906C CA2538906A CA2538906A CA2538906C CA 2538906 C CA2538906 C CA 2538906C CA 2538906 A CA2538906 A CA 2538906A CA 2538906 A CA2538906 A CA 2538906A CA 2538906 C CA2538906 C CA 2538906C
- Authority
- CA
- Canada
- Prior art keywords
- morpholinone
- aminophenyl
- preparing
- reaction
- nitrophenyl
- 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.)
- Expired - Lifetime
Links
- MHCRLDZZHOVFEE-UHFFFAOYSA-N 4-(4-aminophenyl)morpholin-3-one Chemical compound C1=CC(N)=CC=C1N1C(=O)COCC1 MHCRLDZZHOVFEE-UHFFFAOYSA-N 0.000 title claims abstract description 21
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 9
- 238000006243 chemical reaction Methods 0.000 claims abstract description 19
- OWMGEFWSGOTGAU-UHFFFAOYSA-N 4-(4-nitrophenyl)morpholin-3-one Chemical compound C1=CC([N+](=O)[O-])=CC=C1N1C(=O)COCC1 OWMGEFWSGOTGAU-UHFFFAOYSA-N 0.000 claims abstract description 18
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 8
- 239000001257 hydrogen Substances 0.000 claims abstract description 8
- 239000003054 catalyst Substances 0.000 claims abstract description 6
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 6
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims abstract description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 19
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 18
- SIWXCJHUZAEIAE-UHFFFAOYSA-N 4-phenylmorpholin-3-one Chemical compound O=C1COCCN1C1=CC=CC=C1 SIWXCJHUZAEIAE-UHFFFAOYSA-N 0.000 claims description 16
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 16
- 239000000047 product Substances 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 7
- VGCXGMAHQTYDJK-UHFFFAOYSA-N Chloroacetyl chloride Chemical compound ClCC(Cl)=O VGCXGMAHQTYDJK-UHFFFAOYSA-N 0.000 claims description 6
- MWGATWIBSKHFMR-UHFFFAOYSA-N 2-anilinoethanol Chemical compound OCCNC1=CC=CC=C1 MWGATWIBSKHFMR-UHFFFAOYSA-N 0.000 claims description 5
- 238000000605 extraction Methods 0.000 claims description 3
- 239000000706 filtrate Substances 0.000 claims description 3
- 238000002425 crystallisation Methods 0.000 claims description 2
- 230000008025 crystallization Effects 0.000 claims description 2
- 230000000802 nitrating effect Effects 0.000 claims description 2
- 238000006396 nitration reaction Methods 0.000 claims description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 4
- 235000011121 sodium hydroxide Nutrition 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- BMPDCQVRKDNUAP-UHFFFAOYSA-N 5-chlorothiophene-2-carbonyl chloride Chemical compound ClC(=O)C1=CC=C(Cl)S1 BMPDCQVRKDNUAP-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 229910017604 nitric acid Inorganic materials 0.000 description 3
- 239000012074 organic phase Substances 0.000 description 3
- 229910052763 palladium Inorganic materials 0.000 description 3
- 229940083608 sodium hydroxide Drugs 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- KGFYHTZWPPHNLQ-AWEZNQCLSA-N rivaroxaban Chemical compound S1C(Cl)=CC=C1C(=O)NC[C@@H]1OC(=O)N(C=2C=CC(=CC=2)N2C(COCC2)=O)C1 KGFYHTZWPPHNLQ-AWEZNQCLSA-N 0.000 description 2
- 229910000104 sodium hydride Inorganic materials 0.000 description 2
- 239000001117 sulphuric acid Substances 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- 238000010626 work up procedure Methods 0.000 description 2
- VPVXHAANQNHFSF-UHFFFAOYSA-N 1,4-dioxan-2-one Chemical compound O=C1COCCO1 VPVXHAANQNHFSF-UHFFFAOYSA-N 0.000 description 1
- WFQDTOYDVUWQMS-UHFFFAOYSA-N 1-fluoro-4-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=C(F)C=C1 WFQDTOYDVUWQMS-UHFFFAOYSA-N 0.000 description 1
- FHQRDEDZJIFJAL-UHFFFAOYSA-N 4-phenylmorpholine Chemical compound C1COCCN1C1=CC=CC=C1 FHQRDEDZJIFJAL-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- -1 aliphatic alcohols Chemical class 0.000 description 1
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 239000003114 blood coagulation factor Substances 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000005595 deprotonation Effects 0.000 description 1
- 238000010537 deprotonation reaction Methods 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- VEUUMBGHMNQHGO-UHFFFAOYSA-N ethyl chloroacetate Chemical compound CCOC(=O)CCl VEUUMBGHMNQHGO-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- VSEAAEQOQBMPQF-UHFFFAOYSA-N morpholin-3-one Chemical compound O=C1COCCN1 VSEAAEQOQBMPQF-UHFFFAOYSA-N 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 230000009424 thromboembolic effect Effects 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
- C07D265/30—1,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings
- C07D265/32—1,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings with oxygen atoms directly attached to ring carbon atoms
-
- 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10342570A DE10342570A1 (de) | 2003-09-15 | 2003-09-15 | Verfahren zur Herstellung von 4-(4-Aminophenyl)-3-morpholinon |
| DE10342570.5 | 2003-09-15 | ||
| PCT/EP2004/010054 WO2005026135A1 (de) | 2003-09-15 | 2004-09-09 | Verfahren zur herstellung von 4-(4-aminophenyl)-3-morpholinon |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2538906A1 CA2538906A1 (en) | 2005-03-24 |
| CA2538906C true CA2538906C (en) | 2013-04-23 |
Family
ID=34305779
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2538906A Expired - Lifetime CA2538906C (en) | 2003-09-15 | 2004-09-09 | Process for preparing 4-(4-aminophenyl)-3-morpholinone |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US7598378B2 (forum.php) |
| EP (1) | EP1664004B1 (forum.php) |
| JP (1) | JP4852419B2 (forum.php) |
| KR (1) | KR101148264B1 (forum.php) |
| CN (1) | CN100430384C (forum.php) |
| AU (1) | AU2004272255B2 (forum.php) |
| BR (1) | BRPI0414382B1 (forum.php) |
| CA (1) | CA2538906C (forum.php) |
| CY (1) | CY1116644T1 (forum.php) |
| DE (1) | DE10342570A1 (forum.php) |
| DK (1) | DK1664004T3 (forum.php) |
| EG (1) | EG26605A (forum.php) |
| ES (1) | ES2545072T3 (forum.php) |
| HU (1) | HUE025273T2 (forum.php) |
| IL (1) | IL174194A (forum.php) |
| IN (1) | IN2012DN00411A (forum.php) |
| MX (1) | MXPA06002883A (forum.php) |
| PL (1) | PL1664004T3 (forum.php) |
| PT (1) | PT1664004E (forum.php) |
| SI (1) | SI1664004T1 (forum.php) |
| WO (1) | WO2005026135A1 (forum.php) |
| ZA (1) | ZA200602093B (forum.php) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100898361B1 (ko) | 2008-07-03 | 2009-05-20 | 주식회사 레고켐 바이오사이언스 | Ｐ4 위치에 사이클릭 아미독심 또는 사이클릭 아미드라존기를 가지는 ＦＸａ 저해제, 이의 유도체, 제조방법 및이를 함유하는 의약 조성물 |
| US7816355B1 (en) | 2009-04-28 | 2010-10-19 | Apotex Pharmachem Inc | Processes for the preparation of rivaroxaban and intermediates thereof |
| CN102822167A (zh) * | 2010-01-04 | 2012-12-12 | 埃南蒂亚有限公司 | 用于制备利伐沙班的方法及其中间体 |
| DE102010018299A1 (de) * | 2010-04-23 | 2011-10-27 | Archimica Gmbh | Verfahren zur Herstellung von 4-(4-Aminophenyl)-morpholin-3-on |
| WO2012032533A2 (en) * | 2010-09-07 | 2012-03-15 | Symed Labs Limited | Processes for the preparation of 4-{4-[5(s)-(aminomethyl)-2-oxo-1,3-oxazolidin-3-yl]phenyl} morpholin-3-one |
| EP2630143B1 (en) | 2010-10-18 | 2017-11-29 | Apotex Pharmachem Inc. | Processes for the preparation of rivaroxaban and intermediates thereof |
| US9221771B2 (en) | 2011-04-11 | 2015-12-29 | Sandoz Ag | Method for the preparation of substituted oxazolidinones |
| EP2705028B1 (en) * | 2011-05-06 | 2019-08-21 | Egis Gyógyszergyár Zrt. | Process for the preparation of a rivaroxaban and intermediates formed in said process |
| WO2012156983A1 (en) * | 2011-05-16 | 2012-11-22 | Symed Labs Limited | Processes for the preparation of 5-chloro-n-({(5s)-2-oxo-3-[4-(3-oxo-4-morpholinyl) phenyl]-1,3-oxazolidin-5-yl}methyl)-2-thiophenecarboxamide |
| CN102320988B (zh) * | 2011-06-03 | 2014-04-09 | 中国科学院上海有机化学研究所 | 4-(4-氨基苯基)-3-吗啉酮中间体酰胺、合成方法和用途 |
| CN103288814B (zh) * | 2012-02-24 | 2016-07-06 | 国药集团国瑞药业有限公司 | 一种利伐沙班中间体的制备方法 |
| CN102746288B (zh) * | 2012-07-24 | 2015-04-08 | 常州制药厂有限公司 | 一种抗凝血药及其关键中间体的制备方法 |
| IN2013MU01113A (forum.php) | 2013-03-25 | 2015-06-19 | Glenmark Generics Ltd | |
| KR20140127651A (ko) * | 2013-04-25 | 2014-11-04 | 주식회사 종근당 | 4-(4-아미노페닐)-3-모폴리논의 신규한 제조 방법 |
| CN103232446B (zh) * | 2013-05-17 | 2015-09-23 | 天津药物研究院 | 一种噁唑烷酮衍生物晶型ⅱ及其制备方法和用途 |
| EP3066098A1 (de) | 2013-11-08 | 2016-09-14 | Bayer Pharma Aktiengesellschaft | Substituierte uracile und ihre verwendung |
| CN103709116B (zh) * | 2013-12-10 | 2015-09-23 | 四川大学 | 一种4-(4-烷氧羰氨基)苯基-3-吗啉酮的制备方法 |
| CN103755657B (zh) * | 2013-12-25 | 2015-10-14 | 湖南方盛制药股份有限公司 | 一种利伐沙班中间体的制备方法 |
| CN104974059B (zh) * | 2014-04-14 | 2016-11-16 | 北大方正集团有限公司 | 一种利伐沙班中间体及其制备方法 |
| CN105085370B (zh) * | 2014-04-22 | 2017-04-12 | 北大方正集团有限公司 | (s)‑1‑卤代‑2‑[2‑(1,3‑二氧异吲哚)基]乙基氯甲酸酯及其制备方法 |
| WO2016030669A1 (en) | 2014-08-25 | 2016-03-03 | Cipla Limited | Process for the preparation of rivaroxaban |
| CN104478820B (zh) * | 2014-12-22 | 2016-08-31 | 杭州瀚康生物医药科技有限公司 | 一种利伐沙班中间体的制备方法 |
| CN104817548B (zh) * | 2015-03-19 | 2017-12-01 | 郑州轻工业学院 | 一种对氢氧化锂、氢氧化钠、氢氧化钾可视化选择性识别的有机小分子 |
| HU231119B1 (hu) | 2018-01-12 | 2020-11-30 | Richter Gedeon Nyrt. | Eljárás 4-(4-aminofenil)morfolin-3-on előállítására |
| CN109651287A (zh) * | 2019-01-18 | 2019-04-19 | 吕东 | 一种4-(4-氨基苯基)吗啉酮的制备方法 |
| US12168167B2 (en) * | 2023-01-11 | 2024-12-17 | Kenneth W. Rittmann | Golf club head cover device |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3279880A (en) | 1965-07-12 | 1966-10-18 | Eastman Kodak Co | Polyester textile material dyed with 1-hydroxy-4-n-p-(2'-pyrrolidonyl-1-) phenyl-amino anthraquinones |
| GB8528633D0 (en) * | 1985-11-21 | 1985-12-24 | Beecham Group Plc | Compounds |
| JPH10503768A (ja) * | 1994-08-02 | 1998-04-07 | メルク シヤープ エンド ドーム リミテツド | アゼチジン、ピロリジンおよびピペリジン誘導体 |
| JP2000514061A (ja) * | 1996-06-28 | 2000-10-24 | メルク エンド カンパニー インコーポレーテッド | フィブリノーゲン受容体拮抗物質 |
| DE19962924A1 (de) | 1999-12-24 | 2001-07-05 | Bayer Ag | Substituierte Oxazolidinone und ihre Verwendung |
| DE10105989A1 (de) * | 2001-02-09 | 2002-08-14 | Bayer Ag | Substituierte Oxazolidinone und ihre Verwendung |
| DE10129725A1 (de) * | 2001-06-20 | 2003-01-02 | Bayer Ag | Kombinationstherapie substituierter Oxazolidinone |
| EP1479676A1 (en) * | 2003-05-19 | 2004-11-24 | Aventis Pharma Deutschland GmbH | Benzimidazole-derivatives as factor xa inhibitors |
| EP1479675A1 (en) * | 2003-05-19 | 2004-11-24 | Aventis Pharma Deutschland GmbH | Indazole-derivatives as factor Xa inhibitors |
-
2003
- 2003-09-15 DE DE10342570A patent/DE10342570A1/de not_active Withdrawn
-
2004
- 2004-09-09 BR BRPI0414382-5A patent/BRPI0414382B1/pt not_active IP Right Cessation
- 2004-09-09 AU AU2004272255A patent/AU2004272255B2/en not_active Expired
- 2004-09-09 PT PT47649900T patent/PT1664004E/pt unknown
- 2004-09-09 EP EP04764990.0A patent/EP1664004B1/de not_active Expired - Lifetime
- 2004-09-09 CA CA2538906A patent/CA2538906C/en not_active Expired - Lifetime
- 2004-09-09 HU HUE04764990A patent/HUE025273T2/en unknown
- 2004-09-09 US US10/571,364 patent/US7598378B2/en active Active
- 2004-09-09 KR KR1020067005136A patent/KR101148264B1/ko not_active Expired - Lifetime
- 2004-09-09 MX MXPA06002883A patent/MXPA06002883A/es active IP Right Grant
- 2004-09-09 PL PL04764990T patent/PL1664004T3/pl unknown
- 2004-09-09 SI SI200432262T patent/SI1664004T1/sl unknown
- 2004-09-09 IN IN411DEN2012 patent/IN2012DN00411A/en unknown
- 2004-09-09 DK DK04764990.0T patent/DK1664004T3/en active
- 2004-09-09 WO PCT/EP2004/010054 patent/WO2005026135A1/de active Application Filing
- 2004-09-09 ES ES04764990.0T patent/ES2545072T3/es not_active Expired - Lifetime
- 2004-09-09 JP JP2006525762A patent/JP4852419B2/ja not_active Expired - Lifetime
- 2004-09-09 CN CNB200480026537XA patent/CN100430384C/zh not_active Expired - Lifetime
-
2006
- 2006-03-09 IL IL174194A patent/IL174194A/en active IP Right Grant
- 2006-03-13 ZA ZA200602093A patent/ZA200602093B/en unknown
- 2006-03-13 EG EGPCTNA2006000246A patent/EG26605A/en active
-
2015
- 2015-08-25 CY CY20151100741T patent/CY1116644T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IN2012DN00411A (forum.php) | 2015-08-21 |
| DE10342570A1 (de) | 2005-04-14 |
| CA2538906A1 (en) | 2005-03-24 |
| KR101148264B1 (ko) | 2012-05-21 |
| PL1664004T3 (pl) | 2015-11-30 |
| IL174194A0 (en) | 2006-08-01 |
| KR20060070561A (ko) | 2006-06-23 |
| PT1664004E (pt) | 2015-09-21 |
| DK1664004T3 (en) | 2015-09-07 |
| WO2005026135A1 (de) | 2005-03-24 |
| EP1664004B1 (de) | 2015-06-24 |
| EP1664004A1 (de) | 2006-06-07 |
| US20070066611A1 (en) | 2007-03-22 |
| HK1098134A1 (zh) | 2007-07-13 |
| EG26605A (en) | 2014-03-23 |
| IL174194A (en) | 2010-11-30 |
| AU2004272255A1 (en) | 2005-03-24 |
| CY1116644T1 (el) | 2017-03-15 |
| ES2545072T3 (es) | 2015-09-08 |
| SI1664004T1 (sl) | 2015-10-30 |
| ZA200602093B (en) | 2007-05-30 |
| US7598378B2 (en) | 2009-10-06 |
| JP2007505821A (ja) | 2007-03-15 |
| MXPA06002883A (es) | 2006-06-05 |
| HUE025273T2 (en) | 2016-02-29 |
| AU2004272255B2 (en) | 2011-01-06 |
| CN1852902A (zh) | 2006-10-25 |
| CN100430384C (zh) | 2008-11-05 |
| BRPI0414382A (pt) | 2006-11-21 |
| BRPI0414382B1 (pt) | 2014-01-28 |
| JP4852419B2 (ja) | 2012-01-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2538906C (en) | Process for preparing 4-(4-aminophenyl)-3-morpholinone | |
| CN101959870B (zh) | 吗啉衍生物的制备 | |
| CN101166728B (zh) | 制备烷基n-酰基苯胺的方法 | |
| HUE025533T2 (en) | A process for preparing an intermediate of dabigatran etexylate | |
| TWI309651B (en) | Method for the manufacture of anagrelide | |
| CZ2014471A3 (cs) | Způsob přípravy vortioxetinu | |
| KR100391870B1 (ko) | N-아릴히드록실아민및n-헤타릴히드록실아민의제조방법 | |
| JPWO2011001976A1 (ja) | スレオ−３−（３，４−ジヒドロキシフェニル）−ｌ−セリンの製造法 | |
| KR101907706B1 (ko) | 아나그렐리드 및 그의 유사체의 제조방법 | |
| JP7532420B2 (ja) | ４－フェニル－５－アルコキシカルボニル－２－チアゾール－２－イル－１，４－ジヒドロピリミジン－６－イル］メチル］－３－オキソ－５，６，８，８ａ－テトラヒドロ－１Ｈ－イミダゾ［１，５－ａ］ピラジン－２－イル］－カルボン酸を調製するための代替方法 | |
| EP2909167B1 (en) | Process for the manufacture of 4-aminobenzoamidine dihydrochloride | |
| HK1098134B (en) | Method for the production of 4-(4-aminophenyl)-3-morpholinon | |
| CN108101899A (zh) | IDO1抑制剂Epacadostat中间体的制备方法 | |
| WO2023100110A1 (en) | Process for preparing brivaracetam | |
| CN118878430A (zh) | 化合物、其合成方法及5,6-二羟基吲哚的合成方法 | |
| JP4568824B2 (ja) | ジアリールスルホン酸誘導体の製造方法 | |
| KR101421032B1 (ko) | (2-메틸-1-(3-메틸벤질)-1Ｈ-벤조[d]이미다졸-5일)(피페리딘-5-일)메탄온의 제조방법 | |
| WO2003101971A1 (en) | Process for preparing (s)-tetrahydro-a-(1-methylethyl)-2-oxo-1(2h)- pyrimidineacetic acid | |
| CN102531987B (zh) | (s)‑3‑氨基吡咯烷二盐酸盐的合成方法 | |
| KR20100088870A (ko) | 3,4-디히드로퀴나졸린-4-온 유도체의 새로운 제조방법 | |
| JPS6322567A (ja) | 新規ピリミジン化合物および該化合物を用いる２−低級アルキル−４−アミノ−５−アミノメチルピリミジンの製造法 | |
| CN102531987A (zh) | (s)-3-氨基吡咯烷二盐酸盐的合成方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request |