ES391026A1 - Benzonaphthyridine derivatives - Google Patents
Benzonaphthyridine derivativesInfo
- Publication number
- ES391026A1 ES391026A1 ES391026A ES391026A ES391026A1 ES 391026 A1 ES391026 A1 ES 391026A1 ES 391026 A ES391026 A ES 391026A ES 391026 A ES391026 A ES 391026A ES 391026 A1 ES391026 A1 ES 391026A1
- Authority
- ES
- Spain
- Prior art keywords
- carbon atoms
- formula
- hydrogen
- chlorine
- trifluoromethyl
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/56—Nitrogen atoms
- C07D211/58—Nitrogen atoms attached in position 4
-
- 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
- C07D491/12—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 three hetero rings
- C07D491/14—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Procedure for obtaining benzonaphthyridine of formula I ** (See formula) ** wherein R1 is hydrogen, C1-3alkyl, C1-3alkoxy or C1-3alkylthio, fluorine, chlorine, bromine, nitro, trifluoromethyl, amino or 2-4 amido carbon atoms, R2 is hydrogen, chlorine, alkyl of 1 to 3 carbon atoms or alkoxy of 1 to 3 carbon atoms, and R3 and R4 signify each other hydrogen or methoxy, or R3 and R4 together are methylenedioxy, characterized by that a 3,4-cis-substituted compound of formula II is cyclized, ** (See formula) ** where R2, R3, and R4 have the meanings indicated above, and RI1 is hydrogen, alkyl of 1 to 3 carbon atoms, alkoxy of 1 to 3 carbon atoms or alkylthio of 1 to 3 carbon atoms, fluorine, chlorine, bromine, nitro or trifluoromethyl, with a dehydrating condensing agent, acid, to obtain a compound of formula Ia, ** (See formula) ** where RI1, R2, R3 and R4 have the meanings indicated above. (Machine-translation by Google Translate, not legally binding)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH708670A CH527196A (en) | 1970-05-13 | 1970-05-13 | Process for the preparation of new benzonaphthyridine derivatives |
CH708970A CH527822A (en) | 1970-05-13 | 1970-05-13 | Cis-1,2,,3,4,4a-10b-hexahydro-2-methyl-6-phenyl benzo - (c) (1,6) naphthyridine derivs |
Publications (1)
Publication Number | Publication Date |
---|---|
ES391026A1 true ES391026A1 (en) | 1974-04-01 |
Family
ID=25700728
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES391026A Expired ES391026A1 (en) | 1970-05-13 | 1971-05-11 | Benzonaphthyridine derivatives |
Country Status (14)
Country | Link |
---|---|
JP (1) | JPS5432799B1 (en) |
AT (1) | AT326674B (en) |
CA (1) | CA970377A (en) |
CS (2) | CS162753B2 (en) |
DE (1) | DE2123328A1 (en) |
DK (1) | DK134488B (en) |
ES (1) | ES391026A1 (en) |
FI (1) | FI52089C (en) |
FR (1) | FR2100649B1 (en) |
GB (1) | GB1361441A (en) |
NL (1) | NL7106502A (en) |
PL (1) | PL76913B1 (en) |
SE (1) | SE387640B (en) |
SU (1) | SU423296A3 (en) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3899494A (en) * | 1970-05-13 | 1975-08-12 | Sandoz Ltd | Substituted 6-phenyl benzo-naphthyridines |
NL7314396A (en) * | 1972-10-26 | 1974-05-01 | ||
BE880455A (en) * | 1979-01-22 | 1980-06-06 | Sandoz Sa | PHARMACEUTICAL COMPOSITIONS BASED ON A BENZO (C) (1,6) NAPHTYRIDINE |
JP2002502403A (en) | 1997-06-03 | 2002-01-22 | ビイク グルデン ロンベルク ヒエーミツシエ フアブリーク ゲゼルシヤフト ミツト ベシユレンクテル ハフツング | Benzonaphthyridine |
SK287231B6 (en) | 1999-08-21 | 2010-04-07 | Nycomed Gmbh | Medicament comprising a PDE inhibitor and a beta2 adrenoreceptor agonist |
US7772188B2 (en) | 2003-01-28 | 2010-08-10 | Ironwood Pharmaceuticals, Inc. | Methods and compositions for the treatment of gastrointestinal disorders |
BRPI0409229A (en) | 2003-04-01 | 2006-03-28 | Applied Research Systems | phosphodiesterase inhibitors in infertility |
JP2007537233A (en) * | 2004-05-12 | 2007-12-20 | ファイザー・プロダクツ・インク | Piperidine derivatives as NK1 and NK3 antagonists |
US8969514B2 (en) | 2007-06-04 | 2015-03-03 | Synergy Pharmaceuticals, Inc. | Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases |
CA2688161C (en) | 2007-06-04 | 2020-10-20 | Kunwar Shailubhai | Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders |
ES2522968T3 (en) | 2008-06-04 | 2014-11-19 | Synergy Pharmaceuticals Inc. | Guanylate cyclase agonists useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders |
ES2624828T3 (en) | 2008-07-16 | 2017-07-17 | Synergy Pharmaceuticals Inc. | Guanylate cyclase agonists useful for the treatment of gastrointestinal disorders, inflammation, cancer and others |
US9616097B2 (en) | 2010-09-15 | 2017-04-11 | Synergy Pharmaceuticals, Inc. | Formulations of guanylate cyclase C agonists and methods of use |
CN108676076A (en) | 2011-03-01 | 2018-10-19 | 辛纳吉制药公司 | The method for preparing guanosine cyclic mono-phosphate agonist |
WO2014131024A2 (en) | 2013-02-25 | 2014-08-28 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase and their uses |
EP2970384A1 (en) | 2013-03-15 | 2016-01-20 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase and their uses |
US9486494B2 (en) | 2013-03-15 | 2016-11-08 | Synergy Pharmaceuticals, Inc. | Compositions useful for the treatment of gastrointestinal disorders |
JP6606491B2 (en) | 2013-06-05 | 2019-11-13 | シナジー ファーマシューティカルズ インコーポレイテッド | Ultra high purity agonist of guanylate cyclase C, method for producing and using the same |
MX2016001714A (en) | 2013-08-09 | 2016-10-03 | Ardelyx Inc | Compounds and methods for inhibiting phosphate transport. |
WO2020237096A1 (en) | 2019-05-21 | 2020-11-26 | Ardelyx, Inc. | Combination for lowering serum phosphate in a patient |
-
1971
- 1971-05-10 GB GB1398471A patent/GB1361441A/en not_active Expired
- 1971-05-11 CS CS341671A patent/CS162753B2/cs unknown
- 1971-05-11 CS CS920771A patent/CS167202B2/cs unknown
- 1971-05-11 DK DK225771A patent/DK134488B/en unknown
- 1971-05-11 DE DE19712123328 patent/DE2123328A1/en not_active Ceased
- 1971-05-11 PL PL14807271A patent/PL76913B1/en unknown
- 1971-05-11 FI FI129371A patent/FI52089C/en active
- 1971-05-11 ES ES391026A patent/ES391026A1/en not_active Expired
- 1971-05-11 SU SU1656559A patent/SU423296A3/en active
- 1971-05-12 NL NL7106502A patent/NL7106502A/xx not_active Application Discontinuation
- 1971-05-12 SE SE613471A patent/SE387640B/en unknown
- 1971-05-12 CA CA112,767A patent/CA970377A/en not_active Expired
- 1971-05-12 AT AT412471A patent/AT326674B/en not_active IP Right Cessation
- 1971-05-12 FR FR7117124A patent/FR2100649B1/fr not_active Expired
- 1971-05-12 JP JP3189471A patent/JPS5432799B1/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
AT326674B (en) | 1975-12-29 |
ATA412471A (en) | 1975-03-15 |
SE387640B (en) | 1976-09-13 |
CS167202B2 (en) | 1976-04-29 |
FI52089B (en) | 1977-02-28 |
FR2100649A1 (en) | 1972-03-24 |
FI52089C (en) | 1977-06-10 |
NL7106502A (en) | 1971-11-16 |
CS162753B2 (en) | 1975-07-15 |
CA970377A (en) | 1975-07-01 |
JPS5432799B1 (en) | 1979-10-16 |
DE2123328A1 (en) | 1971-12-02 |
DK134488B (en) | 1976-11-15 |
DK134488C (en) | 1977-05-16 |
PL76913B1 (en) | 1975-02-28 |
GB1361441A (en) | 1974-07-24 |
SU423296A3 (en) | 1974-04-05 |
FR2100649B1 (en) | 1974-08-30 |
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