FR2321890A1 - Hypotensive amino-quinazoline derivs. - with substd. piperidine or piperazine substit. - Google Patents
Hypotensive amino-quinazoline derivs. - with substd. piperidine or piperazine substit.Info
- Publication number
- FR2321890A1 FR2321890A1 FR7526228A FR7526228A FR2321890A1 FR 2321890 A1 FR2321890 A1 FR 2321890A1 FR 7526228 A FR7526228 A FR 7526228A FR 7526228 A FR7526228 A FR 7526228A FR 2321890 A1 FR2321890 A1 FR 2321890A1
- Authority
- FR
- France
- Prior art keywords
- substd
- piperidine
- amino
- piperazine
- substit
- 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.)
- Granted
Links
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 title abstract 6
- 208000001953 Hypotension Diseases 0.000 title abstract 2
- 208000021822 hypotensive Diseases 0.000 title abstract 2
- 230000001077 hypotensive effect Effects 0.000 title abstract 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 title 2
- CZAAKPFIWJXPQT-UHFFFAOYSA-N quinazolin-2-amine Chemical compound C1=CC=CC2=NC(N)=NC=C21 CZAAKPFIWJXPQT-UHFFFAOYSA-N 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 208000007530 Essential hypertension Diseases 0.000 abstract 1
- 201000004239 Secondary hypertension Diseases 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- VQKLRVZQQYVIJW-UHFFFAOYSA-N dihydralazine Chemical compound C1=CC=C2C(NN)=NN=C(NN)C2=C1 VQKLRVZQQYVIJW-UHFFFAOYSA-N 0.000 abstract 1
- 229960002877 dihydralazine Drugs 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 150000004885 piperazines Chemical class 0.000 abstract 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 230000001988 toxicity Effects 0.000 abstract 1
- 231100000419 toxicity Toxicity 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/40—Acylated substituent nitrogen atom
-
- 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
- C07D211/08—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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/26—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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms
-
- 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
-
- 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
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
- C07D295/205—Radicals derived from carbonic acid
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Quinazoline derivs. of formula (I) and their pharmaceutically acceptable acid addition salts are new. In (I) -N is a piperidine or piperazine nucleus substd. in posn. 3 or 4 by R; R is -(CH2)n-(R1)-COR2, -NR1R3 or -CO2-CH2R4; R1 is H or 1-3C alkyl; R2 is -OR1, phenyl or furyl; n is 0 or 1; R3 is 1-3 C alkyl or R4 is 3-6C cycloalkyl; provided that -N R contains is not 2 N atoms. (I) are hypotensives for human or veterinary use, for treatment of all forms of essential and secondary hypertension. Toxicity is low and activity is comparable with that of dihydrolazine. LD50, rat, p.o., is typically >1 g/kg c.f. 0.44 g/kg for dihydralazine. Daily doses are e.g. 10-400 mg p.o. in units of 5-50 mg or 100 mg parenterally. A typical cpd. is 1-(4-amino-5,6-dimethoxyquinazol-2- )-4-(ethoxycarbonylamino)pip- eridine.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7526228A FR2321890A1 (en) | 1975-08-26 | 1975-08-26 | Hypotensive amino-quinazoline derivs. - with substd. piperidine or piperazine substit. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7526228A FR2321890A1 (en) | 1975-08-26 | 1975-08-26 | Hypotensive amino-quinazoline derivs. - with substd. piperidine or piperazine substit. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| FR2321890A1 true FR2321890A1 (en) | 1977-03-25 |
| FR2321890B1 FR2321890B1 (en) | 1979-09-14 |
Family
ID=9159340
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FR7526228A Granted FR2321890A1 (en) | 1975-08-26 | 1975-08-26 | Hypotensive amino-quinazoline derivs. - with substd. piperidine or piperazine substit. |
Country Status (1)
| Country | Link |
|---|---|
| FR (1) | FR2321890A1 (en) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2919800A1 (en) * | 1978-05-18 | 1979-11-22 | Pfizer | 4-AMINO-2-PIPERIDINOQUINAZOLINE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND MEDICINAL PRODUCTS CONTAINING SUCH DERIVATIVES |
| EP0009465A1 (en) * | 1978-09-20 | 1980-04-02 | Ciba-Geigy Ag | N-(1-(4-amino-2-quinazolinyl)-3 or 4-piperidyl lactames, process for their preparation and pharmaceutical compositions containing them |
| EP0034471A1 (en) * | 1980-02-19 | 1981-08-26 | Orion-Yhtymä Oy | Piperidinoquinazolines and a process for the preparation thereof |
| US4309541A (en) * | 1978-09-20 | 1982-01-05 | Ciba-Geigy Corporation | Piperidinyl-lactams |
| WO1997020820A1 (en) * | 1995-12-01 | 1997-06-12 | Novartis Ag | Heteroaryl compounds |
| US5675006A (en) * | 1992-08-31 | 1997-10-07 | Brantford Chemicals Inc. | Methods of making ureas and guanidines, including, terazosin, prazosin, doxazosin, tiodazosin, trimazosin, quinazosin, and bunazosin (exemplary of 2- substituted quinazoline compounds), and meobentine, and bethanidine and intermediates therefor |
| WO2002048124A3 (en) * | 2000-12-15 | 2003-06-05 | Hoffmann La Roche | Piperazine derivatives |
| WO2005000305A1 (en) * | 2003-06-20 | 2005-01-06 | Eli Lilly And Company | 3-aminopiperidines and 3-aminoquinuclidines as inhibitors of monoamine uptake |
| WO2009107571A1 (en) * | 2008-02-27 | 2009-09-03 | 住友化学株式会社 | Method for optical resolution of alkylpiperidin-3-yl carbamate and intermediate therefor |
| WO2009119700A1 (en) * | 2008-03-26 | 2009-10-01 | 住友化学株式会社 | Manufacturing method for a piperidine-3-ylcarbamate compound and optical resolution method therefor |
| JP2009256337A (en) * | 2008-03-26 | 2009-11-05 | Sumitomo Chemical Co Ltd | Method for producing piperidin-3-ylcarbamate compound |
| CN107814792A (en) * | 2016-09-14 | 2018-03-20 | 中国科学院上海药物研究所 | A kind of quinazoline derivant, its composition and purposes |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3511836A (en) * | 1967-12-13 | 1970-05-12 | Pfizer & Co C | 2,4,6,7-tetra substituted quinazolines |
-
1975
- 1975-08-26 FR FR7526228A patent/FR2321890A1/en active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3511836A (en) * | 1967-12-13 | 1970-05-12 | Pfizer & Co C | 2,4,6,7-tetra substituted quinazolines |
Cited By (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2919800A1 (en) * | 1978-05-18 | 1979-11-22 | Pfizer | 4-AMINO-2-PIPERIDINOQUINAZOLINE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND MEDICINAL PRODUCTS CONTAINING SUCH DERIVATIVES |
| EP0009465A1 (en) * | 1978-09-20 | 1980-04-02 | Ciba-Geigy Ag | N-(1-(4-amino-2-quinazolinyl)-3 or 4-piperidyl lactames, process for their preparation and pharmaceutical compositions containing them |
| US4309541A (en) * | 1978-09-20 | 1982-01-05 | Ciba-Geigy Corporation | Piperidinyl-lactams |
| EP0034471A1 (en) * | 1980-02-19 | 1981-08-26 | Orion-Yhtymä Oy | Piperidinoquinazolines and a process for the preparation thereof |
| US5675006A (en) * | 1992-08-31 | 1997-10-07 | Brantford Chemicals Inc. | Methods of making ureas and guanidines, including, terazosin, prazosin, doxazosin, tiodazosin, trimazosin, quinazosin, and bunazosin (exemplary of 2- substituted quinazoline compounds), and meobentine, and bethanidine and intermediates therefor |
| US5686612A (en) * | 1992-08-31 | 1997-11-11 | Brantford Chemicals Inc. | Methods of making ureas and guanidines, including terazosin, prazosin, doxazosin, tiodazosin, trimazosin, quinazosin, and bunazosin (exemplary of 2-substituted quinazoline compounds), and meobentine, and bethanidine and intermediates thereof |
| US6080860A (en) * | 1992-08-31 | 2000-06-27 | Brantford Chemicalss Inc. | Methods of making ureas and guanidines including, terazosin, prazosin, doxazosin, tiodazosin, trimazosin, quinazosin and bunazosin (exemplary of 2-substituted quinazoline compounds), and meobentine, and bethanidine and intermediates therefor |
| WO1997020820A1 (en) * | 1995-12-01 | 1997-06-12 | Novartis Ag | Heteroaryl compounds |
| WO2002048124A3 (en) * | 2000-12-15 | 2003-06-05 | Hoffmann La Roche | Piperazine derivatives |
| US7022707B2 (en) | 2000-12-15 | 2006-04-04 | Hoffman-La Roche Inc. | Piperazine derivatives |
| WO2005000305A1 (en) * | 2003-06-20 | 2005-01-06 | Eli Lilly And Company | 3-aminopiperidines and 3-aminoquinuclidines as inhibitors of monoamine uptake |
| US7432280B2 (en) | 2003-06-20 | 2008-10-07 | Eli Lilly And Company | 3-aminopiperidines and 3-aminoquinuclidines as inhibitors of monoamine uptake |
| WO2009107571A1 (en) * | 2008-02-27 | 2009-09-03 | 住友化学株式会社 | Method for optical resolution of alkylpiperidin-3-yl carbamate and intermediate therefor |
| JP2009227665A (en) * | 2008-02-27 | 2009-10-08 | Sumitomo Chemical Co Ltd | Method for optical resolution of alkylpiperidin-3-yl carbamate and intermediate therefor |
| WO2009119700A1 (en) * | 2008-03-26 | 2009-10-01 | 住友化学株式会社 | Manufacturing method for a piperidine-3-ylcarbamate compound and optical resolution method therefor |
| JP2009256337A (en) * | 2008-03-26 | 2009-11-05 | Sumitomo Chemical Co Ltd | Method for producing piperidin-3-ylcarbamate compound |
| JP2009256298A (en) * | 2008-03-26 | 2009-11-05 | Sumitomo Chemical Co Ltd | Optical resolution method for piperidin-3-ylcarbamate compound, and its intermediate |
| CN107814792A (en) * | 2016-09-14 | 2018-03-20 | 中国科学院上海药物研究所 | A kind of quinazoline derivant, its composition and purposes |
| CN107814792B (en) * | 2016-09-14 | 2021-08-10 | 中国科学院上海药物研究所 | Quinazoline derivative, composition and application thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2321890B1 (en) | 1979-09-14 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| ST | Notification of lapse |