AR073892A1 - Proceso de preparacion de inhibidores de sglt - Google Patents
Proceso de preparacion de inhibidores de sgltInfo
- Publication number
- AR073892A1 AR073892A1 ARP090103994A ARP090103994A AR073892A1 AR 073892 A1 AR073892 A1 AR 073892A1 AR P090103994 A ARP090103994 A AR P090103994A AR P090103994 A ARP090103994 A AR P090103994A AR 073892 A1 AR073892 A1 AR 073892A1
- Authority
- AR
- Argentina
- Prior art keywords
- ring
- optionally substituted
- formula
- compound
- substituted unsaturated
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title abstract 3
- 102000000070 Sodium-Glucose Transport Proteins Human genes 0.000 title 1
- 108010080361 Sodium-Glucose Transport Proteins Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 9
- 125000000623 heterocyclic group Chemical group 0.000 abstract 7
- 125000002618 bicyclic heterocycle group Chemical group 0.000 abstract 5
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 abstract 4
- 125000002950 monocyclic group Chemical group 0.000 abstract 4
- 150000001555 benzenes Chemical group 0.000 abstract 3
- 238000000034 method Methods 0.000 abstract 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 239000003960 organic solvent Substances 0.000 abstract 2
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 abstract 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 abstract 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
- 102000018711 Facilitative Glucose Transport Proteins Human genes 0.000 abstract 1
- 108091052347 Glucose transporter family Proteins 0.000 abstract 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 abstract 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 abstract 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 150000001721 carbon Chemical group 0.000 abstract 1
- 230000001419 dependent effect Effects 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 210000000936 intestine Anatomy 0.000 abstract 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract 1
- 210000003734 kidney Anatomy 0.000 abstract 1
- 229910052744 lithium Inorganic materials 0.000 abstract 1
- 239000011777 magnesium Substances 0.000 abstract 1
- 229910052749 magnesium Inorganic materials 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/12—Radicals substituted by halogen atoms or nitro or nitroso radicals
-
- 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
- A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
- A61K31/381—Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
-
- 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
-
- 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
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
- C07H13/02—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids
- C07H13/04—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids having the esterifying carboxyl radicals attached to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H7/00—Compounds containing non-saccharide radicals linked to saccharide radicals by a carbon-to-carbon bond
- C07H7/04—Carbocyclic radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Diabetes (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Endocrinology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Hematology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Emergency Medicine (AREA)
- Obesity (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
- Saccharide Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
La presente está dirigida a un proceso para la preparacion de compuestos que tienen actividad inhibitoria contra el transportador de glucosa dependiente de sodio (SGLT) presente en el intestino o en el rinon. Reivindicacion 1: Un proceso para la preparacion de compuestos de formula (1), en donde el Anillo A y el Anillo B son uno de los siguientes: (1) el Anillo A es un anillo heterocíclico monocíclico insaturado opcionalmente sustituido y el Anillo B es un anillo heterocíclico monocíclico insaturado opcionalmente sustituido, anillo heterobicíclico fusionado insaturado opcionalmente sustituido, o un anillo de benceno opcionalmente sustituido; o (2) el Anillo A es un anillo de benceno opcionalmente sustituido, y el Anillo B es un anillo heterocíclico monocíclico insaturado opcionalmente sustituido o un anillo heterobicíclico fusionado insaturado opcionalmente sustituido, en donde Y está enlazado al anillo heterocíclico del anillo heterobicíclico fusionado; o (3) el Anillo A es un anillo heterobicíclico fusionado insaturado opcionalmente sustituido, en donde tanto la porcion azucar X-(azucar) como la porcion -Y-Anillo B) están en el mismo anillo heterocíclico del anillo heterobicíclico fusionado, y el Anillo B es un anillo heterocíclico monocíclico insaturado opcionalmente sustituido, un anillo heterobicíclico fusionado insaturado opcionalmente sustituido o un anillo de benceno opcionalmente sustituido; X es un átomo de carbono; Y es -(CH2)n-, en donde n es 1 o 2; siempre y cuando en el Anillo A, X sea parte de un enlace insaturado; o una sal o solvato farmacéuticamente aceptable de éste; el proceso comprende: hacer reaccionar un compuesto de formula (10), en donde Q0 es bromo o yodo, con un complejo de di(alquil C1-4) magnesio con cloruro de litio o un complejo de C1-4 cloruro de alquilmagnesio con cloruro de litio o un complejo de C1-4 bromuro de alquilmagnesio con cloruro de litio en un solvente orgánico o mezcla de éste a una temperatura que varía desde aproximadamente la temperatura ambiente hasta aproximadamente -78sC para obtener el compuesto de formula (11) correspondiente, en donde Q1 es el MgCl o MgBr correspondiente; o hacer reaccionar el compuesto de formula (11) con un compuesto de formula (12), en donde Z es un grupo protector de oxígeno, en un solvente orgánico o mezcla de éste a una temperatura que varía desde aproximadamente la temperatura ambiente hasta aproximadamente -78°C para obtener el compuesto de formula (13) correspondiente; hacer reaccionar el compuesto de formula (13) para obtener el compuesto de formula (1) correspondiente.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10626008P | 2008-10-17 | 2008-10-17 | |
US10623108P | 2008-10-17 | 2008-10-17 | |
US12/578,934 US9056850B2 (en) | 2008-10-17 | 2009-10-14 | Process for the preparation of compounds useful as inhibitors of SGLT |
Publications (1)
Publication Number | Publication Date |
---|---|
AR073892A1 true AR073892A1 (es) | 2010-12-09 |
Family
ID=42106967
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP090103994A AR073892A1 (es) | 2008-10-17 | 2009-10-16 | Proceso de preparacion de inhibidores de sglt |
Country Status (30)
Country | Link |
---|---|
US (1) | US9056850B2 (es) |
EP (3) | EP2457908B8 (es) |
JP (3) | JP6123111B2 (es) |
KR (2) | KR101679593B1 (es) |
CN (3) | CN105541814A (es) |
AR (1) | AR073892A1 (es) |
AU (1) | AU2009305413B2 (es) |
BR (1) | BRPI0920356B1 (es) |
CA (2) | CA2946212C (es) |
CL (1) | CL2011000849A1 (es) |
CY (3) | CY1113867T1 (es) |
DK (3) | DK2346888T3 (es) |
EA (1) | EA021373B1 (es) |
ES (3) | ES2399959T3 (es) |
HK (1) | HK1224289A1 (es) |
HR (3) | HRP20130254T1 (es) |
HU (2) | HUE030868T2 (es) |
IL (2) | IL212270A0 (es) |
LT (2) | LT2457908T (es) |
MX (1) | MX2011004054A (es) |
NZ (1) | NZ592204A (es) |
PL (3) | PL2346888T3 (es) |
PT (3) | PT2457908T (es) |
RS (3) | RS52740B (es) |
SI (3) | SI2457908T1 (es) |
SM (2) | SMT201300058B (es) |
TW (3) | TWI588143B (es) |
UA (1) | UA107450C2 (es) |
WO (1) | WO2010043682A2 (es) |
ZA (1) | ZA201103587B (es) |
Families Citing this family (51)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EA020209B1 (ru) * | 2007-09-10 | 2014-09-30 | Янссен Фармацевтика Н.В. | Способ получения соединений, применимых в качестве ингибиторов натрийзависимого переносчика глюкозы |
US9056850B2 (en) * | 2008-10-17 | 2015-06-16 | Janssen Pharmaceutica N.V. | Process for the preparation of compounds useful as inhibitors of SGLT |
US20110009347A1 (en) * | 2009-07-08 | 2011-01-13 | Yin Liang | Combination therapy for the treatment of diabetes |
PT2451797E (pt) | 2009-07-10 | 2013-06-25 | Janssen Pharmaceutica Nv | Processo de cristalização para o 1-(β-d-glucopiranosilo)-4-metilo-3-[5-(4-fluorofenilo)-2-tienilometilo]benzeno |
SG10201500258WA (en) * | 2009-10-14 | 2015-03-30 | Janssen Pharmaceutica Nv | Process for the preparation of compounds useful as inhibitors of sglt2 |
US8163704B2 (en) | 2009-10-20 | 2012-04-24 | Novartis Ag | Glycoside derivatives and uses thereof |
KR101931209B1 (ko) * | 2010-05-11 | 2018-12-20 | 얀센 파마슈티카 엔.브이. | Sglt의 억제제로서 1-(베타-d-글루코피라노실)-2-티에닐-메틸벤젠 유도체를 포함하는 약학 제형 |
ES2609791T3 (es) * | 2010-07-06 | 2017-04-24 | Janssen Pharmaceutica, N.V. | Fórmula para tratamientos de co-terapia de diabetes |
KR101913587B1 (ko) | 2011-04-13 | 2018-10-31 | 얀센 파마슈티카 엔.브이. | Sglt2의 억제제로서 유용한 화합물의 제조 방법 |
TWI542596B (zh) | 2011-05-09 | 2016-07-21 | 健生藥品公司 | (2s,3r,4r,5s,6r)-2-(3-((5-(4-氟苯基)噻吩-2-基)甲基)-4-甲基苯基)-6-(羥甲基)四氫-2h-哌喃-3,4,5-三醇之l-脯胺酸及檸檬酸共晶體 |
US9193751B2 (en) | 2012-04-10 | 2015-11-24 | Theracos, Inc. | Process for the preparation of benzylbenzene SGLT2 inhibitors |
WO2013152476A1 (en) * | 2012-04-10 | 2013-10-17 | Theracos, Inc. | Process for the preparation of benzylbenzene sglt2 inhibitors |
MX355831B (es) | 2013-05-08 | 2018-05-02 | Lek Pharmaceuticals | NOVEDOSOS HIDRATOS CRISTALINOS DE 1-(ß-D-GLUCOPIRANOSIL)-4-METIL-3 -[5-(4-FLUORO-FENIL)-2-TIENIL-METIL]-BENCENO. |
CN104418834B (zh) * | 2013-08-23 | 2017-09-15 | 重庆博腾制药科技股份有限公司 | 一种抗糖尿病药物中间体的合成方法 |
CN104418847A (zh) * | 2013-09-10 | 2015-03-18 | 天津药物研究院 | 4-(6-脱氧-β-D-吡喃葡萄糖基)-2-[5-(4-氟苯基)噻吩-2-甲基]-1-甲基苯的制备工艺 |
CN103601715B (zh) * | 2013-11-22 | 2015-08-19 | 沈阳化工大学 | 一种2-(4-氟苯基)噻吩的分离提纯方法 |
EP2918579A1 (en) | 2014-03-14 | 2015-09-16 | LEK Pharmaceuticals d.d. | Synthesis of 2-arylmethyl-5-aryl-thiophene |
EP2933255A1 (en) | 2014-04-17 | 2015-10-21 | LEK Pharmaceuticals d.d. | Novel crystalline form of 1-(beta-D-glucopyranosyl)-4- methyl-3-[5-(4-fluorophenyl)-2-thienylmethyl]benzene |
EP3148979B1 (en) * | 2014-05-27 | 2019-02-06 | Glenmark Pharmaceuticals Limited | Process for preparation of canagliflozin |
CN105330706B (zh) * | 2014-06-05 | 2019-04-16 | 江苏豪森药业集团有限公司 | 卡格列净中间体的制备方法 |
CN104119324B (zh) * | 2014-07-23 | 2016-03-30 | 齐鲁天和惠世制药有限公司 | 一种卡格列净的制备方法 |
CN104292209A (zh) * | 2014-09-11 | 2015-01-21 | 浙江丽晶化学有限公司 | 一种制备2-(4-氟苯基)噻吩(化合物v)的新方法 |
CN104402946B (zh) * | 2014-11-17 | 2018-01-02 | 连云港恒运药业有限公司 | 卡格列净中间体及其无定形的制备方法 |
WO2016083790A1 (en) * | 2014-11-25 | 2016-06-02 | Cipla Limited | Process for the preparation of canagliflozin |
CN105753910A (zh) * | 2014-12-16 | 2016-07-13 | 康普药业股份有限公司 | 一种卡格列净中间体的制备方法 |
CN105753827A (zh) * | 2014-12-17 | 2016-07-13 | 中美华世通生物医药科技(武汉)有限公司 | 制备化合物的方法 |
WO2016128995A1 (en) | 2015-02-09 | 2016-08-18 | Indoco Remedies Limited | Process for the preparation of sglt inhibitor compounds |
WO2016132355A1 (en) * | 2015-02-16 | 2016-08-25 | B. G. Negev Technologies And Applications Ltd., At Ben-Gurion University | Introduction of alkyl substituents to aromatic compounds |
WO2016135747A2 (en) * | 2015-02-27 | 2016-09-01 | Msn Laboratories Private Limited | Process for the preparation of amorphous (1s)-1,5-anhvdro-1-[3-[[5-(4 fluorophennyl)-2-thienyl]methvl]-4-methylphenyl]-d-glucitol and its polymorphs thereof |
WO2016191173A1 (en) | 2015-05-22 | 2016-12-01 | Janssen Pharmaceutica Nv | Anhydrous crystalline form of (1s)-1,5-anhydro-1-[3-[[5-(4-fluorophenyl)-2-thienyl]methyl]-4-methylphenyl]-d-glucitol |
US20170071970A1 (en) | 2015-09-15 | 2017-03-16 | Janssen Pharmaceutica Nv | Co-therapy comprising canagliflozin and phentermine for the treatment of obesity and obesity related disorders |
CZ2015729A3 (cs) | 2015-10-13 | 2017-04-26 | Zentiva, K.S. | Příprava intermediátů pro syntézu Canagliflozinu a Dapagliflozinu |
CN106938998B (zh) * | 2017-04-07 | 2018-07-03 | 四川智强医药科技开发有限公司 | 卡格列净有关物质的合成方法 |
WO2018207113A1 (en) | 2017-05-09 | 2018-11-15 | Piramal Enterprises Limited | A process for the preparation of sglt2 inhibitor and intermediates thereof |
CN109553609B (zh) * | 2017-09-26 | 2020-09-04 | 北大方正集团有限公司 | 一种卡格列净的制备方法 |
WO2019230864A1 (ja) | 2018-05-31 | 2019-12-05 | 株式会社トクヤマ | ジアリールメタン化合物の製造方法 |
JP7046868B2 (ja) * | 2018-05-31 | 2022-04-04 | 株式会社トクヤマ | ジアリールメタン化合物の製造方法 |
JPWO2020050361A1 (ja) * | 2018-09-06 | 2021-08-30 | 株式会社トクヤマ | β−C−アリールグリコシド誘導体の製造方法 |
CN109180662A (zh) * | 2018-10-17 | 2019-01-11 | 北大医药股份有限公司 | 一种卡格列净的制备方法 |
JP2022028986A (ja) * | 2018-12-17 | 2022-02-17 | 株式会社トクヤマ | C-アリールヒドロキシグリコキシド誘導体の製造方法 |
WO2020129899A1 (ja) * | 2018-12-17 | 2020-06-25 | 株式会社トクヤマ | C-アリールヒドロキシグリコキシド誘導体の製造方法 |
CN110698468B (zh) * | 2019-09-24 | 2020-11-03 | 杭州华东医药集团新药研究院有限公司 | 一种坎格列净的制备方法 |
CN111057049B (zh) * | 2019-11-18 | 2021-06-01 | 杭州华东医药集团新药研究院有限公司 | 一种卡格列净半水化合物的制备方法 |
CN113943329A (zh) * | 2020-07-16 | 2022-01-18 | 尚科生物医药(上海)有限公司 | 一种坎格列净中间体的非对映异构体的制备方法 |
EP4249462A4 (en) | 2020-11-18 | 2024-10-16 | Tokuyama Corp | PROCESS FOR PRODUCING A KETONE DERIVATIVE |
CN112608299A (zh) * | 2020-12-24 | 2021-04-06 | 山东铂源药业有限公司 | 一种4-(6-氨基吡啶-3-基)哌啶-1-甲酸叔丁酯的合成方法 |
CN113372326A (zh) * | 2021-06-23 | 2021-09-10 | 江苏法安德医药科技有限公司 | 一种2-(4-氟苯基)噻吩的分离提纯方法 |
CN113429379A (zh) * | 2021-06-28 | 2021-09-24 | 江苏法安德医药科技有限公司 | 一种lh-1801中间体及其制备方法和应用 |
JPWO2023080243A1 (es) * | 2021-11-08 | 2023-05-11 | ||
CN115557940B (zh) * | 2022-12-06 | 2023-06-20 | 恒升德康(南京)医药科技有限公司 | 一种利用微通道反应器连续化生产卡格列净的方法 |
CN116789716A (zh) * | 2023-06-26 | 2023-09-22 | 南京科默生物医药有限公司 | 一种达格列净和艾托格列净中间体的制备方法 |
Family Cites Families (138)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2799241A (en) * | 1949-01-21 | 1957-07-16 | Wisconsin Alumni Res Found | Means for applying coatings to tablets or the like |
US4160861A (en) * | 1977-10-03 | 1979-07-10 | Merck & Co., Inc. | Method for the separation of antibiotic macrolides |
US4584369A (en) * | 1981-07-31 | 1986-04-22 | Sloan-Kettering Institute For Cancer Research | Anti-leukemic beta-glycosyl C-nucleosides |
JPS5939889A (ja) | 1982-08-30 | 1984-03-05 | Noguchi Kenkyusho | 2,4,6↓−トリ↓−0↓−アセチル↓−3↓−デオキシ↓−ヘキソノ↓−1,5↓−ラクトンの製造方法 |
JP2544609B2 (ja) | 1986-10-07 | 1996-10-16 | 和光純薬工業株式会社 | Tcnq錯体 |
US4863957A (en) | 1987-12-21 | 1989-09-05 | Rorer Pharmaceutical Corporation | Novel HMG-CoA reductase inhibitors |
CA1327013C (en) | 1988-06-23 | 1994-02-15 | Peter Rex Brawn | Cosmetic composition |
CA1334969C (en) | 1988-08-19 | 1995-03-28 | Mark James Suto | Substituted dihydroisoquinoline and phthalazine derivatives as potentiators of the lethal effects of radiation and certain chemotherapeutic agents, selected compounds, analogs andprocess |
DK0472502T3 (da) * | 1990-08-24 | 1995-10-09 | Spirig Ag | Fremgangsmåde til fremstilling af pellets |
JPH04253974A (ja) | 1991-02-05 | 1992-09-09 | Ishihara Sangyo Kaisha Ltd | スルホニル尿素系化合物、それらの製造方法及びそれらを含有する除草剤 |
EP0517969A1 (en) * | 1991-06-10 | 1992-12-16 | AUSIMONT S.p.A. | Process for increasing the bleaching efficiency of an inorganic persalt or of hydrogen peroxide |
US5149838A (en) * | 1991-09-20 | 1992-09-22 | Merck & Co., Inc. | Intermediates for substituted azetidinones useful as anti-inflammatory and antidegenerative agents |
US5610294A (en) * | 1991-10-11 | 1997-03-11 | The Du Pont Merck Pharmaceutical Company | Substituted cyclic carbonyls and derivatives thereof useful as retroviral protease inhibitors |
CN1071924A (zh) | 1991-10-29 | 1993-05-12 | 纳幕尔杜邦公司 | 除草的三唑羧酸酰胺 |
GB9208161D0 (en) | 1992-04-14 | 1992-05-27 | Pfizer Ltd | Indoles |
US5334225A (en) | 1992-07-15 | 1994-08-02 | Kao Corporation | Keratinous fiber dye composition containing a 2-substituted amino-5-alkylphenol derivative coupler |
CA2102591C (en) * | 1992-11-12 | 2000-12-26 | Kenji Tsujihara | Hypoglycemic agent |
US5731292A (en) * | 1992-11-12 | 1998-03-24 | Tanabe Seiyaku Co., Ltd. | Dihydrochalcone derivatives which are hypoglycemic agents |
DE4243279A1 (de) * | 1992-12-21 | 1994-06-23 | Bayer Ag | Substituierte Triole |
US6297363B1 (en) * | 1993-02-12 | 2001-10-02 | Nomura Co., Ltd. | Glycoside indoles |
JPH06256354A (ja) | 1993-03-01 | 1994-09-13 | Nippon Nohyaku Co Ltd | 新規テトラゾール化合物及びその製法 |
JP3187611B2 (ja) | 1993-05-17 | 2001-07-11 | キヤノン株式会社 | 液晶性化合物、これを含む液晶組成物、それを有する液晶素子、それらを用いた表示方法および表示装置 |
JPH07242526A (ja) | 1994-03-03 | 1995-09-19 | Sogo Yatsukou Kk | 化粧料 |
US5830873A (en) * | 1994-05-11 | 1998-11-03 | Tanabe Seiyaku Co., Ltd. | Propiophenone derivative and a process for preparing the same |
WO1996013258A1 (en) | 1994-09-30 | 1996-05-09 | The Ohio State Research Foundation | C-glycoside analogues of n-(4-hydroxyphenyl)retinamide-o-glucuronide |
US5780483A (en) * | 1995-02-17 | 1998-07-14 | Smithkline Beecham Corporation | IL-8 receptor antagonists |
WO1997025033A1 (en) | 1995-10-31 | 1997-07-17 | Eli Lilly And Company | Antithrombotic diamines |
JP3059088B2 (ja) * | 1995-11-07 | 2000-07-04 | 田辺製薬株式会社 | プロピオフェノン誘導体およびその製法 |
US5723495A (en) | 1995-11-16 | 1998-03-03 | The University Of North Carolina At Chapel Hill | Benzamidoxime prodrugs as antipneumocystic agents |
JPH09263549A (ja) | 1996-01-25 | 1997-10-07 | Fujisawa Pharmaceut Co Ltd | ベンゼン誘導体の製造法 |
IL121525A0 (en) * | 1996-08-26 | 1998-02-08 | Tanabe Seiyaku Co | Process for preparing optically active benzothiazepine compound and intermediate therefor |
TW406086B (en) * | 1996-12-26 | 2000-09-21 | Tanabe Seiyaku Co | Propiophenone derivatives and process for preparing the same |
US6153632A (en) * | 1997-02-24 | 2000-11-28 | Rieveley; Robert B. | Method and composition for the treatment of diabetes |
AU6422298A (en) | 1997-03-25 | 1998-10-20 | Takeda Chemical Industries Ltd. | Pharmaceutical composition containing a phosphorylamide and an ayntibiotic |
CN1203846C (zh) * | 1998-03-19 | 2005-06-01 | 布里斯托尔-迈尔斯斯奎布公司 | 高溶解性药物的双相控释递送系统和方法 |
WO1999065861A1 (de) | 1998-06-18 | 1999-12-23 | Merck Patent Gmbh | Verfahren zur symmetrischen und unsymmetrischen disubstitution von carbonsäureamiden mit organotitanaten und grignard-reagenzien |
FR2780403B3 (fr) * | 1998-06-24 | 2000-07-21 | Sanofi Sa | Nouvelle forme de l'irbesartan, procedes pour obtenir ladite forme et compositions pharmaceutiques en contenant |
JP2000034239A (ja) | 1998-07-16 | 2000-02-02 | Asahi Glass Co Ltd | トリフルオロメチル化芳香族化合物の製造方法 |
JP3857429B2 (ja) | 1998-07-17 | 2006-12-13 | ポーラ化成工業株式会社 | 含硫黄抗真菌剤 |
US6069238A (en) * | 1998-09-30 | 2000-05-30 | Eli Lilly And Company | Spirocyclic C-glycosides |
BR9915194A (pt) | 1998-11-09 | 2001-08-07 | Black James Foundation | Composto, método para fabricar o mesmo, composição farmacêutica, e, método para fabricar a mesma |
AU768994B2 (en) | 1998-11-12 | 2004-01-15 | Smithkline Beecham Plc | Pharmaceutical composition for modified release of an insulin sensitiser and another antidiabetic agent |
US20020032164A1 (en) * | 1998-12-30 | 2002-03-14 | Dale Roderic M. K. | Antimicrobial compounds and methods for their use |
GB9912961D0 (en) | 1999-06-03 | 1999-08-04 | Pfizer Ltd | Metalloprotease inhibitors |
US6515117B2 (en) * | 1999-10-12 | 2003-02-04 | Bristol-Myers Squibb Company | C-aryl glucoside SGLT2 inhibitors and method |
PH12000002657B1 (en) | 1999-10-12 | 2006-02-21 | Bristol Myers Squibb Co | C-aryl glucoside SGLT2 inhibitors |
BR0015294A (pt) | 1999-11-03 | 2003-07-15 | Bristol Myers Squibb Co | Método para tratamento da diabetes |
JP3450810B2 (ja) * | 2000-01-31 | 2003-09-29 | キヤノン株式会社 | 脂肪族ポリエステル、脂肪族ポリエステルの製造方法およびセルロースの再資源化方法 |
JP4456768B2 (ja) | 2000-02-02 | 2010-04-28 | 壽製薬株式会社 | C−配糖体を含有する薬剤 |
US6627611B2 (en) * | 2000-02-02 | 2003-09-30 | Kotobuki Pharmaceutical Co Ltd | C-glycosides and preparation of thereof as antidiabetic agents |
BR0108908A (pt) | 2000-03-03 | 2002-12-24 | Pfizer Prod Inc | Derivados de éteres de pirazol como agentes antiinflamatórios/analgésicos |
DE60115623T2 (de) | 2000-03-17 | 2006-07-06 | Kissei Pharmaceutical Co., Ltd., Matsumoto | Glucopyranosyloxy-benzylbenzen-derivate, medizinische zusammensetzung und zwischenprodukte für die herstellung der derivate |
US6555519B2 (en) * | 2000-03-30 | 2003-04-29 | Bristol-Myers Squibb Company | O-glucosylated benzamide SGLT2 inhibitors and method |
US6683056B2 (en) | 2000-03-30 | 2004-01-27 | Bristol-Myers Squibb Company | O-aryl glucoside SGLT2 inhibitors and method |
GB0011098D0 (en) | 2000-05-08 | 2000-06-28 | Black James Foundation | Pharmaceutical compositions comprising protpn pump inhibitors and gastrin/cholecystokinin receptor ligands |
EP1172362A1 (de) | 2000-07-11 | 2002-01-16 | Basf Aktiengesellschaft | Azadioxacycloalkene und ihre Verwendung zur Bekämpfung von Schadpilzen und tierischen Schädlingen |
KR100426030B1 (ko) * | 2000-07-22 | 2004-04-03 | (주) 한켐 | 락톤계 당화합물에서의 키랄성 전환방법 |
WO2002026706A2 (en) | 2000-09-29 | 2002-04-04 | Bayer Pharmaceuticals Corporation | 17-beta-hydroxysteroid dehydrogenase-ii inhibitors |
WO2002036602A1 (fr) | 2000-11-02 | 2002-05-10 | Ajinomoto Co., Inc. | Nouveaux derives du pyrazole et remedes au diabete contenant ces derniers |
JP2002167430A (ja) | 2000-12-01 | 2002-06-11 | Canon Inc | 脂肪族ポリエステル、脂肪族ポリエステルの製造方法およびデンプンの資源化方法 |
US6476352B2 (en) * | 2000-12-18 | 2002-11-05 | General Electric Company | Laser beam stop sensor and method for automatically detecting the presence of laser beam stop material using a laser beam stop sensor |
ES2326158T3 (es) | 2000-12-28 | 2009-10-02 | Kissei Pharmaceutical Co., Ltd. | Derivados de glucopiranosiloxipirazol y su utilizacion como medicamentos. |
US7087579B2 (en) * | 2001-02-26 | 2006-08-08 | Kissei Pharmaceutical Co., Ltd. | Glucopyranosyloxypyrazole derivatives and medicinal use thereof |
US7294618B2 (en) * | 2001-02-27 | 2007-11-13 | Kissei Pharmaceutical Co., Ltd. | Glucopyranosyloxypyrazole derivatives and medicinal use thereof |
CA2710031A1 (en) | 2001-03-02 | 2002-09-12 | University Of Western Ontario | Polymer precursors of radiolabeled compounds, and methods of making and using the same |
US6936590B2 (en) * | 2001-03-13 | 2005-08-30 | Bristol Myers Squibb Company | C-aryl glucoside SGLT2 inhibitors and method |
AU2002254567B2 (en) | 2001-04-11 | 2007-10-11 | Bristol-Myers Squibb Company | Amino acid complexes of C-aryl glucosides for treatment of diabetes and method |
WO2002088157A1 (fr) * | 2001-04-27 | 2002-11-07 | Ajinomoto Co., Inc. | Derives pyrazolyl-o-glycoside n-substitues et medicament contre le diabete en contenant |
GB0112122D0 (en) | 2001-05-18 | 2001-07-11 | Lilly Co Eli | Heteroaryloxy 3-substituted propanamines |
US7105556B2 (en) | 2001-05-30 | 2006-09-12 | Bristol-Myers Squibb Company | Conformationally constrained analogs useful as antidiabetic and antiobesity agents and method |
WO2003000712A1 (fr) | 2001-06-20 | 2003-01-03 | Kissei Pharmaceutical Co., Ltd. | Derive heterocyclique azote, composition medicinale contenant ce derive, leur utilisation medicinale et intermediaire associe |
JP4115105B2 (ja) | 2001-07-02 | 2008-07-09 | 協和醗酵工業株式会社 | ピラゾール誘導体 |
WO2003011880A1 (fr) | 2001-07-31 | 2003-02-13 | Kissei Pharmaceutical Co., Ltd. | Derive de glucopyranosyloxybenzylbenzene, composition medicinale contenant ce derive, usage medicinal de cette composition et produit intermediaire pour produire cette composition |
US20030191121A1 (en) * | 2001-08-09 | 2003-10-09 | Miller Ross A. | Piperazine carboxamide intermediates of HIV protease inhibitors and processes for their preparation |
EP1432720A1 (en) | 2001-09-05 | 2004-06-30 | Bristol-Myers Squibb Company | O-pyrazole glucoside sglt2 inhibitors and method of use |
US7384763B2 (en) * | 2001-10-24 | 2008-06-10 | Michael Burton | Method of detecting β-D-ribofuranosidase activity |
BR0213949A (pt) | 2001-11-08 | 2004-08-31 | Sepracor Inc | Métodos para o tratamento de depressão e outros distúrbios do snc utilizando metabólitos desmetila e didesmetila de citalopram enanciomericamente enriquecidos |
EA009281B1 (ru) | 2001-11-16 | 2007-12-28 | Катаникс Корпорейшн | Фармацевтические и косметические композиции, содержащие ароматические альдегиды, содержащие оксигруппу |
JP2003238417A (ja) | 2002-02-18 | 2003-08-27 | Nippon Shoyaku Kenkyusho:Kk | フロレチン配糖体の安定化組成物、該安定化組成物を含有する糖尿病予防・治療剤、および保健食品 |
US6617313B1 (en) * | 2002-03-13 | 2003-09-09 | Council Of Scientific And Industrial Research | Glucopyranoside and process of isolation thereof from pterocarpus marsupium pharmaceutical composition containing the same and use thereof |
US6562791B1 (en) * | 2002-03-29 | 2003-05-13 | Council Of Scientific And Industrial Research | Glucopyranoside, process for isolation thereof, pharmaceutical composition containing same and use thereof |
JP2003313168A (ja) | 2002-04-18 | 2003-11-06 | Kirin Brewery Co Ltd | Bcl−2阻害活性を有する化合物およびその化合物のスクリーニング方法 |
NZ561993A (en) | 2002-04-18 | 2008-09-26 | Astrazeneca Ab | Spiroazabicyclic heterocyclic amines as potent ligands for nicotinic acetylcholine receptors |
DE10231370B4 (de) * | 2002-07-11 | 2006-04-06 | Sanofi-Aventis Deutschland Gmbh | Thiophenglycosidderivate, diese Verbindungen enthaltende Arzneimittel und Verfahren zur Herstellung dieser Arzneimittel |
TWI254635B (en) | 2002-08-05 | 2006-05-11 | Yamanouchi Pharma Co Ltd | Azulene derivative and salt thereof |
KR20050056194A (ko) | 2002-08-09 | 2005-06-14 | 다이쇼 세이야꾸 가부시끼가이샤 | 선택적인 아릴 5-티오-β-D-알도헥소피라노시드의 제조방법 |
AU2003262262A1 (en) | 2002-08-27 | 2004-03-19 | Kissei Pharmaceutical Co., Ltd. | Pyrazole derivatives, medicinal composition containing the same, and medicinal use thereof |
CA2501239A1 (en) * | 2002-10-07 | 2004-04-22 | Encore Pharmaceuticals, Inc. | R-nsaid esters and their use |
DE10258008B4 (de) | 2002-12-12 | 2006-02-02 | Sanofi-Aventis Deutschland Gmbh | Heterocyclische Fluorglycosidderivate, diese Verbindungen enthaltende Arzneimittel und Verfahren zur Herstellung dieser Arzneimittel |
DE10258007B4 (de) * | 2002-12-12 | 2006-02-09 | Sanofi-Aventis Deutschland Gmbh | Aromatische Fluorglycosidderivate, diese Verbindungen enthaltende Arzneimittel und Verfahren zur Herstellung dieser Arzneimittel |
BR0317929A (pt) | 2003-01-03 | 2006-04-11 | Bristol Myers Squibb Co | métodos de produzir inibidores de sglt2 de glicosìdeo de c-arila |
EP1597266A4 (en) | 2003-02-27 | 2008-02-20 | Bristol Myers Squibb Co | NON-CRYOGENIC PROCESS FOR THE PRODUCTION OF GLYCOSIDES |
PL1609785T3 (pl) * | 2003-03-14 | 2016-07-29 | Astellas Pharma Inc | Pochodne c-glikozydowe i ich sole |
JP2004300102A (ja) | 2003-03-31 | 2004-10-28 | Kissei Pharmaceut Co Ltd | 縮合複素環誘導体、それを含有する医薬組成物およびその医薬用途 |
AU2003902263A0 (en) | 2003-05-12 | 2003-05-29 | Fujisawa Pharmaceutical Co., Ltd. | Monosaccharide compounds |
ES2377741T3 (es) | 2003-06-20 | 2012-03-30 | Kissei Pharmaceutical Co., Ltd. | Derivados de pirazol, composición farmacológica que los contiene e intermedios de producción de los mismos |
AU2004259347B2 (en) | 2003-07-23 | 2011-02-24 | Synta Pharmaceuticals, Corp. | Method for modulating calcium ion-release-activated calcium ion channels |
EA011515B1 (ru) * | 2003-08-01 | 2009-04-28 | Янссен Фармацевтика Н.В. | Замещенные бензимидазол-, бензтриазол- и бензимидазолон-о-глюкозиды |
UA86042C2 (en) * | 2003-08-01 | 2009-03-25 | Янссен Фармацевтика Н.В. | Substituted indazole-o-glucosides |
RS20060320A (en) * | 2003-08-01 | 2008-08-07 | Janssen Pharmaceutica N.V., | Substituted indazole-o-glucosides |
AR048376A1 (es) * | 2003-08-01 | 2006-04-26 | Janssen Pharmaceutica Nv | C- glicosidos heterociclos fusionados sustituidos |
EP1680131A4 (en) * | 2003-08-01 | 2009-05-27 | Janssen Pharmaceutica Nv | SUBSTITUTED INDOLE-O-GLUCOSIDES |
TWI385177B (zh) * | 2003-08-01 | 2013-02-11 | Mitsubishi Tanabe Pharma Corp | 吡喃葡萄糖基衍生物及其製造方法 |
WO2005058845A2 (en) | 2003-12-19 | 2005-06-30 | Novo Nordisk A/S | Novel glucagon antagonists/inverse agonists |
NZ550464A (en) * | 2004-03-16 | 2010-10-29 | Boehringer Ingelheim Int | Glucopyranosyl-substituted benzol derivatives, drugs containing said compounds, the use thereof and method for the production thereof |
US7393836B2 (en) * | 2004-07-06 | 2008-07-01 | Boehringer Ingelheim International Gmbh | D-xylopyranosyl-substituted phenyl derivatives, medicaments containing such compounds, their use and process for their manufacture |
WO2006010557A1 (de) | 2004-07-27 | 2006-02-02 | Boehringer Ingelheim International Gmbh | D-glucopyranosyl-phenyl-substituierte cyclen, diese verbindungen enthaltende arzneimittel, deren verwendung und verfahren zu ihrer herstellung |
WO2006018150A1 (de) * | 2004-08-11 | 2006-02-23 | Boehringer Ingelheim International Gmbh | D-xylopyranosyl-phenyl-substituierte cyclen, diese verbindungen enthaltende arzneimittel, deren verwendung und verfahren zu ihrer herstellung |
TW200637839A (en) * | 2005-01-07 | 2006-11-01 | Taisho Pharmaceutical Co Ltd | 1-thio-d-glucitol derivatives |
WO2006082523A2 (en) * | 2005-01-25 | 2006-08-10 | Aurobindo Pharma Limited | Pharmaceutical sustained release composition of metformin |
AR053329A1 (es) * | 2005-01-31 | 2007-05-02 | Tanabe Seiyaku Co | Derivados de indol utiles como inhibidores de los transportadores de glucosa dependientes del sodio (sglt) |
CA2595257A1 (en) * | 2005-02-23 | 2006-08-31 | Boehringer Ingelheim International Gmbh | Glucopyranosyl-substituted ((hetero)arylethynyl-benzyl)-benzene derivatives and use thereof as sodium-dependent glucose cotransporter 2 (sglt2) inhibitors |
ATE453656T1 (de) | 2005-04-15 | 2010-01-15 | Boehringer Ingelheim Int | Glucopyranosyl-substituierte (heteroaryloxy- benzyl)-benzen-derivate als sglt-inhibitoren |
US7772191B2 (en) * | 2005-05-10 | 2010-08-10 | Boehringer Ingelheim International Gmbh | Processes for preparing of glucopyranosyl-substituted benzyl-benzene derivatives and intermediates therein |
WO2007014894A2 (en) * | 2005-07-27 | 2007-02-08 | Boehringer Ingelheim International Gmbh | Glucopyranosyl-substituted ( (hetero) cycloalyklethynyl-benzyl) -benzene derivatives and use thereof as sodium-dependent glucose cotransporter (sglt) inhibitors |
JP5175191B2 (ja) | 2005-08-30 | 2013-04-03 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | グリコピラノシル置換ベンジルベンゼン誘導体、該化合物を含有する医薬品及びその使用と製造方法 |
AR056195A1 (es) | 2005-09-15 | 2007-09-26 | Boehringer Ingelheim Int | Procedimientos para preparar derivados de (etinil-bencil)-benceno sustituidos de glucopiranosilo y compuestos intermedios de los mismos |
US8741960B2 (en) | 2006-01-25 | 2014-06-03 | Synta Pharmaceuticals Corp. | Substituted aromatic compounds for inflammation and immune-related uses |
JP2007230999A (ja) | 2006-01-31 | 2007-09-13 | Kyoto Univ | 置換芳香族ニトリル化合物およびその製造方法 |
TWI418556B (zh) * | 2006-07-27 | 2013-12-11 | Mitsubishi Tanabe Pharma Corp | 吲哚衍生物 |
EP2054426A1 (en) | 2006-08-15 | 2009-05-06 | Boehringer Ingelheim International GmbH | Glucopyranosyl-substituted cyclopropylbenzene derivatives, pharmaceutical compositions containing such compounds, their use as sglt inhibitors and process for their manufacture |
US7858587B2 (en) | 2006-09-21 | 2010-12-28 | Boehringer Ingelheim International Gmbh | Glucopyranosyl-substituted difluorobenzyl-benzene derivates, medicaments containing such compounds, their use and process for their manufacture |
EP2079753A1 (en) | 2006-11-06 | 2009-07-22 | Boehringer Ingelheim International GmbH | Glucopyranosyl-substituted benzyl-benzonitrile derivatives, medicaments containing such compounds, their use and process for their manufacture |
WO2008055940A2 (en) | 2006-11-09 | 2008-05-15 | Boehringer Ingelheim International Gmbh | Combination therapy with sglt-2 inhibitors and their pharmaceutical compositions |
UY30730A1 (es) * | 2006-12-04 | 2008-07-03 | Mitsubishi Tanabe Pharma Corp | Forma cristalina del hemihidrato de 1-(b (beta)-d-glucopiranosil) -4-metil-3-[5-(4-fluorofenil) -2-tienilmetil]benceno |
ES2397664T3 (es) * | 2006-12-04 | 2013-03-08 | Janssen Pharmaceutica, N.V. | Derivados de glucopiranósilo que contienen tienilo como antidiabéticos |
EP1956023A1 (en) | 2007-02-06 | 2008-08-13 | Lonza Ag | Method for lithium exchange reactions |
AR065809A1 (es) * | 2007-03-22 | 2009-07-01 | Bristol Myers Squibb Co | Formulaciones farmaceuticas que contienen un inhibidor sglt2 |
US20090047514A1 (en) | 2007-08-15 | 2009-02-19 | Allen David P | Thermal Activated Pressure Sensitive Adhesive and Method for Producing the Same and Product therewith |
PE20090603A1 (es) | 2007-08-16 | 2009-06-11 | Boehringer Ingelheim Int | Composicion farmaceutica que comprende un inhibidor de sglt2 y un inhibidor de dpp iv |
WO2009026537A1 (en) | 2007-08-23 | 2009-02-26 | Theracos, Inc. | Benzylbenzene derivatives and methods of use |
EA020209B1 (ru) | 2007-09-10 | 2014-09-30 | Янссен Фармацевтика Н.В. | Способ получения соединений, применимых в качестве ингибиторов натрийзависимого переносчика глюкозы |
CL2008003653A1 (es) | 2008-01-17 | 2010-03-05 | Mitsubishi Tanabe Pharma Corp | Uso de un inhibidor de sglt derivado de glucopiranosilo y un inhibidor de dppiv seleccionado para tratar la diabetes; y composicion farmaceutica. |
PE20140960A1 (es) | 2008-04-03 | 2014-08-15 | Boehringer Ingelheim Int | Formulaciones que comprenden un inhibidor de dpp4 |
US9056850B2 (en) * | 2008-10-17 | 2015-06-16 | Janssen Pharmaceutica N.V. | Process for the preparation of compounds useful as inhibitors of SGLT |
US20110009347A1 (en) * | 2009-07-08 | 2011-01-13 | Yin Liang | Combination therapy for the treatment of diabetes |
SG10201500258WA (en) * | 2009-10-14 | 2015-03-30 | Janssen Pharmaceutica Nv | Process for the preparation of compounds useful as inhibitors of sglt2 |
KR101931209B1 (ko) * | 2010-05-11 | 2018-12-20 | 얀센 파마슈티카 엔.브이. | Sglt의 억제제로서 1-(베타-d-글루코피라노실)-2-티에닐-메틸벤젠 유도체를 포함하는 약학 제형 |
-
2009
- 2009-10-14 US US12/578,934 patent/US9056850B2/en active Active
- 2009-10-15 EP EP12156039.5A patent/EP2457908B8/en active Active
- 2009-10-15 PT PT121560395T patent/PT2457908T/pt unknown
- 2009-10-15 SI SI200931615A patent/SI2457908T1/sl unknown
- 2009-10-15 KR KR1020167017935A patent/KR101679593B1/ko active IP Right Grant
- 2009-10-15 AU AU2009305413A patent/AU2009305413B2/en active Active
- 2009-10-15 RS RS20130121A patent/RS52740B/en unknown
- 2009-10-15 EA EA201170579A patent/EA021373B1/ru unknown
- 2009-10-15 MX MX2011004054A patent/MX2011004054A/es active IP Right Grant
- 2009-10-15 KR KR1020117010834A patent/KR101724598B1/ko active IP Right Grant
- 2009-10-15 DK DK09736928.4T patent/DK2346888T3/da active
- 2009-10-15 ES ES09736928T patent/ES2399959T3/es active Active
- 2009-10-15 EP EP09736928A patent/EP2346888B1/en active Active
- 2009-10-15 PT PT121560353T patent/PT2455374T/pt unknown
- 2009-10-15 WO PCT/EP2009/063503 patent/WO2010043682A2/en active Application Filing
- 2009-10-15 SI SI200932112T patent/SI2455374T1/sl unknown
- 2009-10-15 CN CN201510944228.0A patent/CN105541814A/zh active Pending
- 2009-10-15 UA UAA201106134A patent/UA107450C2/uk unknown
- 2009-10-15 LT LTEP12156039.5T patent/LT2457908T/lt unknown
- 2009-10-15 JP JP2011531489A patent/JP6123111B2/ja active Active
- 2009-10-15 ES ES12156039.5T patent/ES2611881T3/es active Active
- 2009-10-15 PL PL09736928T patent/PL2346888T3/pl unknown
- 2009-10-15 DK DK12156035.3T patent/DK2455374T3/da active
- 2009-10-15 PT PT97369284T patent/PT2346888E/pt unknown
- 2009-10-15 CA CA2946212A patent/CA2946212C/en active Active
- 2009-10-15 CA CA2740853A patent/CA2740853C/en active Active
- 2009-10-15 SI SI200930548T patent/SI2346888T1/sl unknown
- 2009-10-15 DK DK12156039.5T patent/DK2457908T3/en active
- 2009-10-15 HU HUE12156039A patent/HUE030868T2/en unknown
- 2009-10-15 PL PL12156039T patent/PL2457908T3/pl unknown
- 2009-10-15 EP EP12156035.3A patent/EP2455374B1/en active Active
- 2009-10-15 RS RS20170048A patent/RS55577B1/sr unknown
- 2009-10-15 LT LTEP12156035.3T patent/LT2455374T/lt unknown
- 2009-10-15 BR BRPI0920356-7A patent/BRPI0920356B1/pt active IP Right Grant
- 2009-10-15 RS RS20210150A patent/RS61484B1/sr unknown
- 2009-10-15 CN CN2009801516486A patent/CN102264714A/zh active Pending
- 2009-10-15 ES ES12156035T patent/ES2854598T3/es active Active
- 2009-10-15 NZ NZ592204A patent/NZ592204A/xx unknown
- 2009-10-15 PL PL12156035T patent/PL2455374T3/pl unknown
- 2009-10-15 CN CN201310358939.0A patent/CN103467439B/zh active Active
- 2009-10-15 HU HUE12156035A patent/HUE052432T2/hu unknown
- 2009-10-16 TW TW098135070A patent/TWI588143B/zh active
- 2009-10-16 TW TW103123880A patent/TWI636981B/zh active
- 2009-10-16 AR ARP090103994A patent/AR073892A1/es active IP Right Grant
- 2009-10-16 TW TW104122678A patent/TW201613905A/zh unknown
-
2011
- 2011-04-12 IL IL212270A patent/IL212270A0/en unknown
- 2011-04-15 CL CL2011000849A patent/CL2011000849A1/es unknown
- 2011-05-16 ZA ZA2011/03587A patent/ZA201103587B/en unknown
-
2013
- 2013-03-22 HR HRP20130254AT patent/HRP20130254T1/hr unknown
- 2013-03-29 CY CY20131100267T patent/CY1113867T1/el unknown
- 2013-06-05 SM SM201300058T patent/SMT201300058B/xx unknown
-
2014
- 2014-06-17 JP JP2014124295A patent/JP5905926B2/ja active Active
-
2015
- 2015-06-10 IL IL239313A patent/IL239313A/en active IP Right Grant
-
2016
- 2016-03-09 JP JP2016045328A patent/JP2016117758A/ja active Pending
- 2016-11-01 HK HK16112527.9A patent/HK1224289A1/zh unknown
-
2017
- 2017-02-10 SM SM201700092T patent/SMT201700092B/it unknown
- 2017-02-17 HR HRP20170255TT patent/HRP20170255T1/hr unknown
- 2017-02-21 CY CY20171100236T patent/CY1118708T1/el unknown
-
2021
- 2021-02-09 HR HRP20210225TT patent/HRP20210225T1/hr unknown
- 2021-02-15 CY CY20211100125T patent/CY1123817T1/el unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR073892A1 (es) | Proceso de preparacion de inhibidores de sglt | |
Senadi et al. | Iodine-promoted cyclization of N-propynyl amides and N-allyl amides via sulfonylation and sulfenylation | |
AR071246A1 (es) | Proceso para la preparacion de compuestos utiles como inhibidores de sglt | |
UA109883C2 (uk) | Спосіб отримання сполук для застосування як інгібіторів sglt2 | |
RU2015148010A (ru) | Высокоактивное производное нуклеозида для лечения hcv | |
PE20121615A1 (es) | Proceso para la preparacion de intermediarios para la obtencion de inhibidores de nep | |
MA33952B1 (fr) | Nouveau dérivé 3 -hydroxy- 5-arylisothiazole | |
IN2014MN02106A (es) | ||
CR20130534A (es) | Nuevos derivados de imidazol útiles para el tratamiento de artritis | |
NZ597598A (en) | Mesoionic pyridinium compounds containing a five-membered ring fused to the pyridinium ring for controlling invertebrate pests | |
NO20091858L (no) | Hydrobenzamid derivater som inhibitorer av HSP90 | |
AR088564A1 (es) | PROCESO PARA LA PREPARACION DE AGONISTAS Y COMPUESTOS INTERMEDIOS DE b3 | |
EA201400622A1 (ru) | Соединения 2-(замещенный-фенил)циклопентан-1,3-диона и их производные | |
BR112013011593A2 (pt) | cristal de derivado de morfinan 7-carbamoíla-6,7-insaturada e método para produzir o mesmo | |
IN2014DN01993A (es) | ||
CO6300945A2 (es) | Compuestos fenil ftalazin - 1l piperidin - 4 - il benzamida o sales farmaceuticamente aceptables de los mismos, utiles como antagonistas de la trayectoria hedgehoc (hh) | |
AR087683A1 (es) | N-[1-((6-cloropiridin-3-il)metil)piridin-2-(1h)-ilideno]-2,2,2-trifluoroacetamida, metodo para su preparacion y un intermediario para su sintesis | |
CR20110264A (es) | Pirazolilaminopiridinas como inhibidores de fak | |
ES2367332T3 (es) | Agentes antiparasitarios de benzofurano. | |
NO20080739L (no) | Fremgangsmater for behandling av Epileptogenese | |
AR117002A2 (es) | Proceso para la preparación de inhibidores de quinasa c-fms | |
AR076969A1 (es) | Un procedimiento para la preparacion de febuxostat | |
WO2013034780A3 (en) | Process for the preparation of estetrol and related compounds | |
AR064002A1 (es) | Quinazolinas sustituidas | |
AR076516A1 (es) | Derivados de oxa-azaespiro[3.3]heptan-6-ilo, metodo e intermediarios para su preparacion, composiciones farmaceuticas que los comprenden y su uso en el tratamiento de enfermedades mediadas por el receptor mch1. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG | Grant, registration |