FI52089C - A process for the preparation of therapeutically active cis-benzo [c] -1,6 / naphthyridine derivatives. - Google Patents
A process for the preparation of therapeutically active cis-benzo [c] -1,6 / naphthyridine derivatives.Info
- Publication number
- FI52089C FI52089C FI129371A FI129371A FI52089C FI 52089 C FI52089 C FI 52089C FI 129371 A FI129371 A FI 129371A FI 129371 A FI129371 A FI 129371A FI 52089 C FI52089 C FI 52089C
- Authority
- FI
- Finland
- Prior art keywords
- benzo
- preparation
- therapeutically active
- naphthyridine derivatives
- active cis
- Prior art date
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)
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 (2)
Publication Number | Publication Date |
---|---|
FI52089B FI52089B (en) | 1977-02-28 |
FI52089C true FI52089C (en) | 1977-06-10 |
Family
ID=25700728
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI129371A FI52089C (en) | 1970-05-13 | 1971-05-11 | A process for the preparation of therapeutically active cis-benzo [c] -1,6 / naphthyridine 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 |
PT1212089E (en) | 1999-08-21 | 2006-08-31 | Altana Pharma Ag | ROFLUMILAST AND SALMETEROL SYNERGY COMBINATION |
US7772188B2 (en) | 2003-01-28 | 2010-08-10 | Ironwood Pharmaceuticals, Inc. | Methods and compositions for the treatment of gastrointestinal disorders |
JP2006522151A (en) | 2003-04-01 | 2006-09-28 | アプライド リサーチ システムズ エーアールエス ホールディング ナームロゼ フェンノートシャップ | 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 |
US20100120694A1 (en) | 2008-06-04 | 2010-05-13 | Synergy Pharmaceuticals, Inc. | Agonists of Guanylate Cyclase Useful for the Treatment of Gastrointestinal Disorders, Inflammation, Cancer and Other Disorders |
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 |
CA3089569C (en) | 2007-06-04 | 2023-12-05 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders |
EP2321341B1 (en) | 2008-07-16 | 2017-02-22 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase useful for the treatment of gastrointestinal, inflammation, cancer and other disorders |
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 |
JP6499591B2 (en) | 2013-02-25 | 2019-04-10 | 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 | Guanylate cyclase receptor agonists for use in colon lavage |
EP2970384A1 (en) | 2013-03-15 | 2016-01-20 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase and their uses |
JP2016514670A (en) | 2013-03-15 | 2016-05-23 | 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 | Guanylate cyclase receptor agonists in combination with other drugs |
RS65632B1 (en) | 2013-06-05 | 2024-07-31 | Bausch Health Ireland Ltd | Ultra-pure agonists of guanylate cyclase c, method of making and using same |
WO2015021358A2 (en) | 2013-08-09 | 2015-02-12 | Dominique Charmot | Compounds and methods for inhibiting phosphate transport |
JP2022533251A (en) | 2019-05-21 | 2022-07-21 | アルデリックス, インコーポレイテッド | Combinations to lower serum phosphate in patients |
-
1971
- 1971-05-10 GB GB1398471A patent/GB1361441A/en not_active Expired
- 1971-05-11 DK DK225771A patent/DK134488B/en unknown
- 1971-05-11 CS CS341671A patent/CS162753B2/cs unknown
- 1971-05-11 DE DE19712123328 patent/DE2123328A1/en not_active Ceased
- 1971-05-11 CS CS920771A patent/CS167202B2/cs unknown
- 1971-05-11 PL PL14807271A patent/PL76913B1/en unknown
- 1971-05-11 FI FI129371A patent/FI52089C/en active
- 1971-05-11 SU SU1656559A patent/SU423296A3/en active
- 1971-05-11 ES ES391026A patent/ES391026A1/en not_active Expired
- 1971-05-12 FR FR7117124A patent/FR2100649B1/fr not_active Expired
- 1971-05-12 JP JP3189471A patent/JPS5432799B1/ja active Pending
- 1971-05-12 AT AT412471A patent/AT326674B/en not_active IP Right Cessation
- 1971-05-12 SE SE613471A patent/SE387640B/en unknown
- 1971-05-12 NL NL7106502A patent/NL7106502A/xx not_active Application Discontinuation
- 1971-05-12 CA CA112,767A patent/CA970377A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR2100649A1 (en) | 1972-03-24 |
DK134488C (en) | 1977-05-16 |
FI52089B (en) | 1977-02-28 |
CS167202B2 (en) | 1976-04-29 |
AT326674B (en) | 1975-12-29 |
SE387640B (en) | 1976-09-13 |
GB1361441A (en) | 1974-07-24 |
DK134488B (en) | 1976-11-15 |
CS162753B2 (en) | 1975-07-15 |
ES391026A1 (en) | 1974-04-01 |
JPS5432799B1 (en) | 1979-10-16 |
CA970377A (en) | 1975-07-01 |
PL76913B1 (en) | 1975-02-28 |
ATA412471A (en) | 1975-03-15 |
SU423296A3 (en) | 1974-04-05 |
DE2123328A1 (en) | 1971-12-02 |
NL7106502A (en) | 1971-11-16 |
FR2100649B1 (en) | 1974-08-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
FI52089C (en) | A process for the preparation of therapeutically active cis-benzo [c] -1,6 / naphthyridine derivatives. | |
NO140301C (en) | ANALOGICAL PROCEDURE FOR THE PREPARATION OF THERAPEUTICALLY ACTIVE IMIDAZO (5,1-F) -AS-TRIAZINES | |
SE400280B (en) | 2-HALOGEN-4-SUBSTITUTED-6,7,8-TRIALCOXIKINAZOLINES FOR USE AS AN INTERMEDIATE FOR THE PREPARATION OF THERAPEUTICALLY ACTIVE 2-SUBSTITUTED-4-AMINO-6,7,8-TRIALKOXIKINAZ | |
FI49300C (en) | Process for the preparation of therapeutically active 1,4-dihydropyridine derivatives. | |
FI49515C (en) | Process for the preparation of pharmacologically active 11,11-substituted 5,1-dihydro-6H-pyrido [2,3-b] [1,4] benzodiazepin-6-ones. | |
NO138565C (en) | ANALOGICAL PROCEDURE FOR THE PREPARATION OF THERAPEUTICALLY ACTIVE PIPERAZINYL-PROPYL-1,2,4-TRIAZOLINON DERIVATIVES | |
FI49503C (en) | Analogous process for the preparation of 1,2,3,4-tetrahydro-4-phenylisoquinoline derivatives. | |
FI48588C (en) | Analog method for the preparation of therapeutically active 3,4-dihydroisoquinoline derivatives. | |
NO740327L (en) | Analogous process for the preparation of pharmacologically active imidazopyridines. | |
NO741744L (en) | Analogous process for the preparation of new therapeutically active derivatives of naphthyridine. | |
FI49827C (en) | Process for the preparation of therapeutically active substituted 3-hydroxymethylisoquinolines. | |
FI49504C (en) | Process for the preparation of pharmacologically active benzocycloheptaquinoline derivatives. | |
PH12247A (en) | Pharmaceutically active compounds | |
NO136574C (en) | ANALOGICAL PROCEDURE FOR THE PREPARATION OF THERAPEUTICALLY ACTIVE PYRIMIDINE DERIVATIVES. | |
NO740614L (en) | Analogous process for the preparation of therapeutically active 2-phenylaminoimidazoline (2) compounds. | |
SE400768B (en) | PROCEDURE FOR THE PREPARATION OF 2-PHENYL-6-SULFAMOYL-7-CHLORO-1,2,3,4-TETRAHYDRO-4-CHINAZOLINONE | |
NO741752L (en) | Analogous process for the preparation of therapeutically active amino derivatives of pyrazolopyridine ketones. | |
FI49718C (en) | Process for the preparation of therapeutically active 2-halomethyl-3-carboxylic acid amidoquinoxaline di-N-oxides- (1,4). | |
FI51349C (en) | Process for the preparation of therapeutically active N-substituted 6,7-benzomorphans. | |
NO741044L (en) | Analogous process for the preparation of therapeutically active triazines. | |
FI49514C (en) | Process for the preparation of pharmaceutically active 11,11-substituted 5,11-dihydro-6H-pyrido (2,3-b) (1,4) benzodiazepin-6-ones. | |
FI50630C (en) | Process for the preparation of pharmacologically active 2,3,4,4a-tetrahydro-10H-1,2-oxazino (3,2-b) (1,3) benzoxazin-10-ones. | |
FI50629C (en) | A process for the preparation of novel therapeutically active 2,3-dihydro-1H-thieno-Bent warepino (4,5-c) pyrrole compounds. | |
FI47357C (en) | A process for the preparation of therapeutically active 4'-demethyl-epipodophyllotoxin ni-beta-D-glucoside derivatives. | |
FI50875C (en) | Process for the preparation of therapeutically active dihydro-2-aminoisoquinolines. |