SE463154B - 6-fenetylaminoalkyl-furo(3,4-c)pyridinderivat,framstaellning daerav och terapeutiska kompositioner innehaallande dem - Google Patents
6-fenetylaminoalkyl-furo(3,4-c)pyridinderivat,framstaellning daerav och terapeutiska kompositioner innehaallande demInfo
- Publication number
- SE463154B SE463154B SE8504826A SE8504826A SE463154B SE 463154 B SE463154 B SE 463154B SE 8504826 A SE8504826 A SE 8504826A SE 8504826 A SE8504826 A SE 8504826A SE 463154 B SE463154 B SE 463154B
- Authority
- SE
- Sweden
- Prior art keywords
- groups
- carbon atoms
- methyl
- furo
- group
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 7
- 230000001225 therapeutic effect Effects 0.000 title claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 23
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- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 239000000460 chlorine Substances 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 4
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- 238000002360 preparation method Methods 0.000 claims description 3
- IRIKALLDOSHXEN-UHFFFAOYSA-N 2-(7-hydroxyfuro[3,4-c]pyridin-6-yl)-3-methylbutanenitrile Chemical class OC1=C(C(C#N)C(C)C)N=CC2=COC=C21 IRIKALLDOSHXEN-UHFFFAOYSA-N 0.000 claims description 2
- BFJMHTOBRRZELQ-UHFFFAOYSA-N 3-iodo-2h-pyrazolo[3,4-c]pyridine Chemical class N1=CC=C2C(I)=NNC2=C1 BFJMHTOBRRZELQ-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 21
- 125000003545 alkoxy group Chemical group 0.000 claims 9
- 125000000217 alkyl group Chemical group 0.000 claims 9
- 229910052801 chlorine Inorganic materials 0.000 claims 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 3
- 125000004414 alkyl thio group Chemical group 0.000 claims 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims 3
- 125000004663 dialkyl amino group Chemical group 0.000 claims 3
- 125000004984 dialkylaminoalkoxy group Chemical group 0.000 claims 3
- 125000001153 fluoro group Chemical group F* 0.000 claims 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 3
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- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 3
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims 3
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- 125000001544 thienyl group Chemical group 0.000 claims 2
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
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- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 6
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- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 3
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- 239000007858 starting material Substances 0.000 description 3
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- VKPPFDPXZWFDFA-UHFFFAOYSA-N 2-chloroethanamine Chemical compound NCCCl VKPPFDPXZWFDFA-UHFFFAOYSA-N 0.000 description 2
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- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- WSDQIHATCCOMLH-UHFFFAOYSA-N phenyl n-(3,5-dichlorophenyl)carbamate Chemical compound ClC1=CC(Cl)=CC(NC(=O)OC=2C=CC=CC=2)=C1 WSDQIHATCCOMLH-UHFFFAOYSA-N 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229940076279 serotonin Drugs 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 238000012453 sprague-dawley rat model Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
-
- 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
-
- 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/10—Antioedematous agents; Diuretics
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Diabetes (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB848427218A GB8427218D0 (en) | 1984-10-27 | 1984-10-27 | Pyridine derivatives |
Publications (3)
Publication Number | Publication Date |
---|---|
SE8504826D0 SE8504826D0 (sv) | 1985-10-16 |
SE8504826L SE8504826L (sv) | 1986-04-28 |
SE463154B true SE463154B (sv) | 1990-10-15 |
Family
ID=10568857
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SE8504826A SE463154B (sv) | 1984-10-27 | 1985-10-16 | 6-fenetylaminoalkyl-furo(3,4-c)pyridinderivat,framstaellning daerav och terapeutiska kompositioner innehaallande dem |
Country Status (25)
Country | Link |
---|---|
US (1) | US4659719A (en, 2012) |
JP (1) | JPS61289090A (en, 2012) |
AR (1) | AR242212A1 (en, 2012) |
AT (1) | AT394558B (en, 2012) |
BE (1) | BE903438A (en, 2012) |
CA (1) | CA1300151C (en, 2012) |
CH (1) | CH666689A5 (en, 2012) |
DE (1) | DE3538063A1 (en, 2012) |
DK (1) | DK160049C (en, 2012) |
DZ (1) | DZ850A1 (en, 2012) |
ES (1) | ES8609330A1 (en, 2012) |
FI (1) | FI82248C (en, 2012) |
FR (2) | FR2572405B1 (en, 2012) |
GB (2) | GB8427218D0 (en, 2012) |
HK (1) | HK6289A (en, 2012) |
IE (1) | IE59475B1 (en, 2012) |
IT (1) | IT1190413B (en, 2012) |
LU (1) | LU86136A1 (en, 2012) |
MA (1) | MA20558A1 (en, 2012) |
NL (1) | NL8502899A (en, 2012) |
NO (1) | NO162191C (en, 2012) |
OA (1) | OA08128A (en, 2012) |
PT (1) | PT81365B (en, 2012) |
SE (1) | SE463154B (en, 2012) |
ZA (1) | ZA858004B (en, 2012) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8426738D0 (en) * | 1984-10-23 | 1984-11-28 | Scras | Pyridine derivatives |
DE3642331A1 (de) * | 1986-12-11 | 1988-06-23 | Basf Ag | Basisch substituierte phenylacetonitrile, ihre herstellung und diese enthaltende arzneimittel |
GB8808001D0 (en) * | 1988-04-06 | 1988-05-05 | Scras | Stereospecific preparative process for furol(3,4-c)pyridine derivatives |
US5130252A (en) * | 1990-05-14 | 1992-07-14 | Synthetech, Inc. | Resolution of furopyridine enantiomers and synthetic precursors thereof |
EP1207860B1 (en) | 1999-09-02 | 2007-10-24 | Nostrum Pharmaceuticals, Inc. | Controlled release pellet formulation |
US20070095037A1 (en) * | 2007-01-18 | 2007-05-03 | Mclamb Samuel B Iii | Supplementary air filter and retainer |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1551268A (en, 2012) * | 1967-12-07 | 1968-12-27 | ||
ZA786269B (en) * | 1977-11-25 | 1979-10-31 | Scras | New pyridine derivative,its preparation and use |
IN156817B (en, 2012) * | 1981-02-10 | 1985-11-09 | Scras | |
IN160104B (en, 2012) * | 1983-04-05 | 1987-06-27 | Scras | |
GB2137618B (en) * | 1983-04-05 | 1986-05-08 | Scras | Furo-(3,4-c)-pyridine derivatives |
GB8402740D0 (en) * | 1984-02-02 | 1984-03-07 | Scras | Furo-(3 4-c)-pyridine derivatives |
GB8422029D0 (en) * | 1984-08-31 | 1984-10-03 | Scras | 6-substituted-furo-(3 4-c)-pyridine derivatives |
-
1984
- 1984-10-27 GB GB848427218A patent/GB8427218D0/en active Pending
-
1985
- 1985-10-14 BE BE0/215724A patent/BE903438A/fr not_active IP Right Cessation
- 1985-10-15 CH CH4448/85A patent/CH666689A5/fr not_active IP Right Cessation
- 1985-10-16 SE SE8504826A patent/SE463154B/sv not_active IP Right Cessation
- 1985-10-17 ZA ZA858004A patent/ZA858004B/xx unknown
- 1985-10-20 DZ DZ850232A patent/DZ850A1/fr active
- 1985-10-21 GB GB08525939A patent/GB2166136B/en not_active Expired
- 1985-10-21 US US06/789,731 patent/US4659719A/en not_active Expired - Fee Related
- 1985-10-22 AR AR85302019A patent/AR242212A1/es active
- 1985-10-22 MA MA20782A patent/MA20558A1/fr unknown
- 1985-10-23 CA CA000493657A patent/CA1300151C/en not_active Expired - Lifetime
- 1985-10-23 FR FR8515708A patent/FR2572405B1/fr not_active Expired
- 1985-10-23 FR FR8515709A patent/FR2572285B1/fr not_active Expired
- 1985-10-23 NL NL8502899A patent/NL8502899A/nl active Search and Examination
- 1985-10-24 PT PT81365A patent/PT81365B/pt not_active IP Right Cessation
- 1985-10-24 LU LU86136A patent/LU86136A1/fr unknown
- 1985-10-25 NO NO854277A patent/NO162191C/no unknown
- 1985-10-25 DK DK490385A patent/DK160049C/da not_active IP Right Cessation
- 1985-10-25 OA OA58714A patent/OA08128A/xx unknown
- 1985-10-25 DE DE19853538063 patent/DE3538063A1/de active Granted
- 1985-10-25 IE IE264585A patent/IE59475B1/en not_active IP Right Cessation
- 1985-10-25 IT IT22612/85A patent/IT1190413B/it active
- 1985-10-25 FI FI854180A patent/FI82248C/fi not_active IP Right Cessation
- 1985-10-25 ES ES548209A patent/ES8609330A1/es not_active Expired
- 1985-10-26 JP JP60238624A patent/JPS61289090A/ja active Granted
- 1985-10-28 AT AT0310385A patent/AT394558B/de not_active IP Right Cessation
-
1989
- 1989-01-19 HK HK62/89A patent/HK6289A/xx not_active IP Right Cessation
Also Published As
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