NO300893B1 - Etanoladdukter av 6-sulfonylsubstituerte 3-hydroksykromaner og deres anvendelse som inhalasjonsmiddel ved behandling av astma - Google Patents
Etanoladdukter av 6-sulfonylsubstituerte 3-hydroksykromaner og deres anvendelse som inhalasjonsmiddel ved behandling av astma Download PDFInfo
- Publication number
- NO300893B1 NO300893B1 NO924806A NO924806A NO300893B1 NO 300893 B1 NO300893 B1 NO 300893B1 NO 924806 A NO924806 A NO 924806A NO 924806 A NO924806 A NO 924806A NO 300893 B1 NO300893 B1 NO 300893B1
- Authority
- NO
- Norway
- Prior art keywords
- ethanol
- stands
- dimethyl
- substituted
- asthma
- Prior art date
Links
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical class CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 title claims abstract description 36
- 208000006673 asthma Diseases 0.000 title claims abstract description 8
- -1 6-sulfonyl-substituted 3-hydroxychromanes Chemical class 0.000 title description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 239000000654 additive Substances 0.000 claims description 3
- HHFAWKCIHAUFRX-UHFFFAOYSA-N ethoxide Chemical compound CC[O-] HHFAWKCIHAUFRX-UHFFFAOYSA-N 0.000 claims description 2
- 239000000825 pharmaceutical preparation Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 16
- 238000000034 method Methods 0.000 abstract description 5
- 238000002360 preparation method Methods 0.000 abstract description 5
- 201000010099 disease Diseases 0.000 abstract description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 238000002844 melting Methods 0.000 description 9
- 230000008018 melting Effects 0.000 description 9
- 239000000126 substance Substances 0.000 description 8
- 238000004458 analytical method Methods 0.000 description 6
- 229910001868 water Inorganic materials 0.000 description 6
- 150000005827 chlorofluoro hydrocarbons Chemical class 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- LKAQWOWWTKFLNX-UXHICEINSA-N 1-[(3s,4r)-6-(benzenesulfonyl)-3-hydroxy-2,2-dimethyl-3,4-dihydrochromen-4-yl]pyrrolidin-2-one Chemical compound N1([C@@H]2C3=CC(=CC=C3OC([C@H]2O)(C)C)S(=O)(=O)C=2C=CC=CC=2)CCCC1=O LKAQWOWWTKFLNX-UXHICEINSA-N 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 230000008020 evaporation Effects 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000012453 solvate Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 3
- SSYKIVRUEAEMHF-UHFFFAOYSA-N 6-(benzenesulfonyl)-3-bromo-2,2-dimethyl-3,4-dihydrochromen-4-ol Chemical compound C1=C2C(O)C(Br)C(C)(C)OC2=CC=C1S(=O)(=O)C1=CC=CC=C1 SSYKIVRUEAEMHF-UHFFFAOYSA-N 0.000 description 3
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 239000005457 ice water Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000003380 propellant Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- FIVJVQHIVZORQH-UHFFFAOYSA-N 4-amino-6-(benzenesulfonyl)-2,2-dimethyl-3,4-dihydrochromen-3-ol Chemical compound C1=C2C(N)C(O)C(C)(C)OC2=CC=C1S(=O)(=O)C1=CC=CC=C1 FIVJVQHIVZORQH-UHFFFAOYSA-N 0.000 description 2
- KMRSYXCXLIPVBY-UHFFFAOYSA-N 6-(benzenesulfonyl)-2,2-dimethyl-1a,7b-dihydrooxireno[2,3-c]chromene Chemical compound C1=C2C3OC3C(C)(C)OC2=CC=C1S(=O)(=O)C1=CC=CC=C1 KMRSYXCXLIPVBY-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 241000700198 Cavia Species 0.000 description 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 2
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 2
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 2
- IWYDHOAUDWTVEP-UHFFFAOYSA-N R-2-phenyl-2-hydroxyacetic acid Natural products OC(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000012458 free base Substances 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 150000004677 hydrates Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- WEXRUCMBJFQVBZ-UHFFFAOYSA-N pentobarbital Chemical compound CCCC(C)C1(CC)C(=O)NC(=O)NC1=O WEXRUCMBJFQVBZ-UHFFFAOYSA-N 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 230000029058 respiratory gaseous exchange Effects 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000012258 stirred mixture Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- QBYIENPQHBMVBV-HFEGYEGKSA-N (2R)-2-hydroxy-2-phenylacetic acid Chemical compound O[C@@H](C(O)=O)c1ccccc1.O[C@@H](C(O)=O)c1ccccc1 QBYIENPQHBMVBV-HFEGYEGKSA-N 0.000 description 1
- OECHJYYZMSUILG-UHFFFAOYSA-N 1-(benzenesulfonyl)-4-nitrobenzene Chemical compound C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)C1=CC=CC=C1 OECHJYYZMSUILG-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- CDIIZULDSLKBKV-UHFFFAOYSA-N 4-chlorobutanoyl chloride Chemical compound ClCCCC(Cl)=O CDIIZULDSLKBKV-UHFFFAOYSA-N 0.000 description 1
- 206010006482 Bronchospasm Diseases 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- ZDQWESQEGGJUCH-UHFFFAOYSA-N Diisopropyl adipate Chemical compound CC(C)OC(=O)CCCCC(=O)OC(C)C ZDQWESQEGGJUCH-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 150000007514 bases Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000007885 bronchoconstriction Effects 0.000 description 1
- 230000003182 bronchodilatating effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 229960001340 histamine Drugs 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 150000003951 lactams Chemical group 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- IWYDHOAUDWTVEP-UHFFFAOYSA-M mandelate Chemical compound [O-]C(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-M 0.000 description 1
- 229960002510 mandelic acid Drugs 0.000 description 1
- 238000002663 nebulization Methods 0.000 description 1
- 230000000414 obstructive effect Effects 0.000 description 1
- 229960001412 pentobarbital Drugs 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 208000023504 respiratory system disease Diseases 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Pulmonology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicinal Preparation (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrane Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4141350 | 1991-12-14 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO924806D0 NO924806D0 (no) | 1992-12-11 |
| NO924806L NO924806L (no) | 1993-06-15 |
| NO300893B1 true NO300893B1 (no) | 1997-08-11 |
Family
ID=6447111
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO924806A NO300893B1 (no) | 1991-12-14 | 1992-12-11 | Etanoladdukter av 6-sulfonylsubstituerte 3-hydroksykromaner og deres anvendelse som inhalasjonsmiddel ved behandling av astma |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US5310753A (fi) |
| EP (1) | EP0547523B1 (fi) |
| JP (1) | JP2625071B2 (fi) |
| CN (1) | CN1073172A (fi) |
| AT (1) | ATE122674T1 (fi) |
| AU (1) | AU653874B2 (fi) |
| CA (1) | CA2085166A1 (fi) |
| DE (1) | DE59202242D1 (fi) |
| DK (1) | DK0547523T3 (fi) |
| ES (1) | ES2073850T3 (fi) |
| FI (1) | FI925618A (fi) |
| HU (2) | HUT67172A (fi) |
| IL (1) | IL104055A (fi) |
| MX (1) | MX9207216A (fi) |
| NO (1) | NO300893B1 (fi) |
| NZ (1) | NZ245447A (fi) |
| RU (1) | RU2102391C1 (fi) |
| TW (1) | TW244350B (fi) |
| ZA (1) | ZA929616B (fi) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9316111D0 (en) * | 1993-08-04 | 1993-09-22 | Pfizer Ltd | Benzopyrans |
| DE4425255A1 (de) | 1994-07-16 | 1996-01-18 | Asta Medica Ag | Formulierung zur inhalativen Applikation |
| GB9510477D0 (en) * | 1995-05-24 | 1995-07-19 | Sandoz Ltd | Organic compounds |
| FR2756284B1 (fr) * | 1996-11-26 | 2000-04-28 | Adir | Nouveaux derives du benzopyrane, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| US7306789B2 (en) | 2002-11-12 | 2007-12-11 | Warner-Lambert Company, Llc | Method of stimulating hair growth using benzopyrans |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8419515D0 (en) * | 1984-07-31 | 1984-09-05 | Beecham Group Plc | Treatment |
| GB8432063D0 (en) * | 1984-12-19 | 1985-01-30 | Riker Laboratories Inc | Physically modified steroids |
| DE3703227A1 (de) * | 1987-02-04 | 1988-08-18 | Hoechst Ag | Substituierte 3,4-dihydro-2h-benzopyrane, verfahren zu ihrer herstellung, ihre verwendung sowie pharmazeutische praeparate auf basis dieser verbindungen |
| DE3818245A1 (de) * | 1988-05-28 | 1989-12-07 | Hoechst Ag | Kombination von angiotensin-converting-enzyme-hemmern mit kaliumkanal-modulatoren sowie deren verwendung in arzneimitteln |
| FR2633605B1 (fr) * | 1988-07-01 | 1991-07-12 | Rhone Poulenc Chimie | Procede de preparation d'oxyde de titane et d'articles a base d'oxyde de titane |
| DE3824446A1 (de) * | 1988-07-19 | 1990-01-25 | Hoechst Ag, 6230 Frankfurt | Verwendung substituierter 3,4-dihydro-2h-benzopyrane als heilmittel gegen obstruktive funktionsstoerungen der lunge und/oder stoerungen der ableitenden harnwege |
| GB8918298D0 (en) * | 1989-08-10 | 1989-09-20 | Beecham Group Plc | Novel compounds |
-
1992
- 1992-11-27 TW TW081109501A patent/TW244350B/zh active
- 1992-12-10 US US07/988,839 patent/US5310753A/en not_active Expired - Fee Related
- 1992-12-10 FI FI925618A patent/FI925618A/fi unknown
- 1992-12-10 IL IL104055A patent/IL104055A/en not_active IP Right Cessation
- 1992-12-11 CA CA002085166A patent/CA2085166A1/en not_active Abandoned
- 1992-12-11 NO NO924806A patent/NO300893B1/no unknown
- 1992-12-11 JP JP4331334A patent/JP2625071B2/ja not_active Expired - Lifetime
- 1992-12-11 NZ NZ245447A patent/NZ245447A/en unknown
- 1992-12-11 EP EP92121155A patent/EP0547523B1/de not_active Expired - Lifetime
- 1992-12-11 ZA ZA929616A patent/ZA929616B/xx unknown
- 1992-12-11 ES ES92121155T patent/ES2073850T3/es not_active Expired - Lifetime
- 1992-12-11 DK DK92121155.3T patent/DK0547523T3/da active
- 1992-12-11 HU HU9203928A patent/HUT67172A/hu unknown
- 1992-12-11 AU AU30171/92A patent/AU653874B2/en not_active Ceased
- 1992-12-11 MX MX9207216A patent/MX9207216A/es not_active IP Right Cessation
- 1992-12-11 AT AT92121155T patent/ATE122674T1/de active
- 1992-12-11 DE DE59202242T patent/DE59202242D1/de not_active Expired - Fee Related
- 1992-12-14 CN CN92114177A patent/CN1073172A/zh active Pending
- 1992-12-14 HU HU9203928A patent/HU9203928D0/hu unknown
- 1992-12-14 RU RU92004582A patent/RU2102391C1/ru active
Also Published As
| Publication number | Publication date |
|---|---|
| MX9207216A (es) | 1993-06-01 |
| DK0547523T3 (da) | 1995-09-11 |
| DE59202242D1 (de) | 1995-06-22 |
| AU653874B2 (en) | 1994-10-13 |
| CA2085166A1 (en) | 1993-06-15 |
| FI925618A0 (fi) | 1992-12-10 |
| AU3017192A (en) | 1993-06-17 |
| NO924806L (no) | 1993-06-15 |
| TW244350B (fi) | 1995-04-01 |
| US5310753A (en) | 1994-05-10 |
| IL104055A (en) | 1998-04-05 |
| NZ245447A (en) | 1994-09-27 |
| HU9203928D0 (en) | 1993-03-29 |
| ES2073850T3 (es) | 1995-08-16 |
| FI925618A (fi) | 1993-06-15 |
| JP2625071B2 (ja) | 1997-06-25 |
| HUT67172A (en) | 1995-02-28 |
| IL104055A0 (en) | 1993-05-13 |
| NO924806D0 (no) | 1992-12-11 |
| JPH05255303A (ja) | 1993-10-05 |
| ATE122674T1 (de) | 1995-06-15 |
| RU2102391C1 (ru) | 1998-01-20 |
| ZA929616B (en) | 1993-06-18 |
| EP0547523B1 (de) | 1995-05-17 |
| EP0547523A1 (de) | 1993-06-23 |
| CN1073172A (zh) | 1993-06-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US7910573B2 (en) | Crystalline forms of 11β-(4-acetylphenyl)-20,20,21,21,21-pentafluoro-17-hydroxy-19-nor-17α-pregna-4,9-dien-3-one | |
| KR20010088795A (ko) | ＥｔＯ2Ｃ-ＣＨ2-(Ｒ)Ｃｇｌ-Ａｚｅ-Ｐａｂ-ＯＨ의 결정질형태 | |
| US6800635B2 (en) | Crystalline form II of cabergoline | |
| US8884026B2 (en) | Process for preparing rufinamide intermediate | |
| US6680327B2 (en) | Crystalline form VII of cabergoline | |
| NO300893B1 (no) | Etanoladdukter av 6-sulfonylsubstituerte 3-hydroksykromaner og deres anvendelse som inhalasjonsmiddel ved behandling av astma | |
| JPH05221980A (ja) | アセチレン化合物 | |
| AU2002365874A1 (en) | Crystalline venlafaxine base and novel polymorphs of venlafaxine hydrochloride, processes for preparing thereof | |
| WO2019171222A1 (en) | Crystalline forms of venetoclax | |
| KR100254710B1 (ko) | 카르바모일유도체,이것을 함유하는 약학적 조성물 및 이들의 제조방법 | |
| EP0277805A1 (en) | Ergolinyl heterocycles | |
| WO2002060440A1 (en) | Novel forms of 2,3-dimethyl-8-(2-ethyl-6-methylbenzylamino)-imidazo (1,2-a)pyridine-6-carboxamide | |
| US4746666A (en) | Ergoline compounds useful as antiparkinson agents | |
| WO2002060442A1 (en) | Novel forms of 2,3-dimethyl-8-(2-ethyl-6-methylbenzylamino)-imidazo (1,2-a)pyridine-6-carboxamide | |
| WO2024209392A1 (en) | Process for preparing pralsetinib in amorphous form | |
| JPH09165372A (ja) | ２−アザビシクロ［２．２．１］ヘプト−５−エン−３−オンの製造法 | |
| US8338445B2 (en) | Crystal form of cabergoline | |
| WO2023222946A1 (en) | Process for the preparation of cabozantinib | |
| EP1925616A1 (en) | Process for the preparation of crystal forms of cabergoline via stable solvates of cabergoline | |
| EP1384708A1 (en) | Process for the manufacture of form I of nolomirole hydrochloride | |
| JP2005255641A (ja) | ベンゾフラン誘導体 |