GB1348165A - N-n-cyanoalkyl-n-nitroso-amino-amino-alcohol esters - Google Patents
N-n-cyanoalkyl-n-nitroso-amino-amino-alcohol estersInfo
- Publication number
- GB1348165A GB1348165A GB1348165DA GB1348165A GB 1348165 A GB1348165 A GB 1348165A GB 1348165D A GB1348165D A GB 1348165DA GB 1348165 A GB1348165 A GB 1348165A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- nitroso
- acid addition
- formula
- cyanoalkyl
- 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
- 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
- C07D295/22—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 with hetero atoms directly attached to ring nitrogen atoms
- C07D295/28—Nitrogen atoms
- C07D295/30—Nitrogen atoms non-acylated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
1348165 N - [N - (cyanoalkyl) - N - nitroso]- amino-amino alcohol esters SANDOZ Ltd 28 June 1971 [30 June 1970 28 Aug 1970] 30124/71 Heading C2C Novel compounds of Formula I (in which each of R 1 and R 2 is H or C 1-4 alkyl, R 3 is -(R 5 )-CH 2 -X and R 4 is -(R 5 )-CH 3 or -(R 5 )-CH 2 -X, or R 3 and R 4 , together with the N atom, form a radical of Formula II or III in which R 5 is C 1-7 alkylene, X is -ONO 2 or -OCOR 6 , R 6 is C 1-4 alkyl optionally substituted by 1 to 3 F or Cl atoms, R 7 is C 1-3 alkylene, p is 4, 5 or 6 and q is 0 or 1, with the proviso that, in Formula III, when q is 0, the substituent is not on a carbon atom adjacent to the nitrogen atom), and pharmaceutically acceptable acid addition salts thereof, are prepared by (a) nitrating a corresponding compound I in which each X is OH and/or the nitroso group is absent, or (b) acylating a corresponding compound I in which each X is OH by reaction with an appropriate acid anhydride or halide, and, if desired, converting the free bases into acid addition salts. 4 - [N - (2 - cyanoisopropyl) - N - nitroso]- amino - 1 - piperazine - ethanol nitrate is prepared by reacting 4-amino-1-piperazine-ethanol with KCN followed by acetone to give 4-[N- (2 - cyanoisopropyl) - amino] - 1 - piperazineethanol and then nitrating this by treatment with a mixture of acetic anhydride and nitric acid. Pharmaceutical compositions having antianginal activity for oral administration comprise a compound I or a pharmaceutically acceptable acid addition salt thereof, together with a pharmaceutical carrier.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US5133870A | 1970-06-30 | 1970-06-30 | |
US6799470A | 1970-08-28 | 1970-08-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1348165A true GB1348165A (en) | 1974-03-13 |
Family
ID=26729317
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1348165D Expired GB1348165A (en) | 1970-06-30 | 1971-06-28 | N-n-cyanoalkyl-n-nitroso-amino-amino-alcohol esters |
Country Status (4)
Country | Link |
---|---|
CH (1) | CH560178A5 (en) |
DE (1) | DE2131826A1 (en) |
FR (1) | FR2100841B1 (en) |
GB (1) | GB1348165A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0495776A4 (en) * | 1989-02-28 | 1992-02-10 | Us Secretary United States Dep | Stabilized nitric oxide-primary amine complexes useful as cardiovascular agents. |
US5208233A (en) * | 1989-09-15 | 1993-05-04 | The United States Of America As Represented By The Department Of Health And Human Services | Anti-hypertensive compositions of secondary amine-nitric oxide adducts and use thereof |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3921460A1 (en) * | 1989-06-30 | 1991-01-03 | Cassella Ag | SUBSTITUTED 3-AMINO-DYNONOMINES, PROCESS FOR THEIR PREPARATION AND THEIR USE |
DE3921796A1 (en) * | 1989-07-03 | 1991-01-17 | Cassella Ag | SUBSTITUTED 3-AMINO-DYNONOMINES, PROCESS FOR THEIR PREPARATION AND THEIR USE |
-
1971
- 1971-06-18 CH CH892471A patent/CH560178A5/xx not_active IP Right Cessation
- 1971-06-26 DE DE19712131826 patent/DE2131826A1/en active Pending
- 1971-06-28 GB GB1348165D patent/GB1348165A/en not_active Expired
- 1971-06-29 FR FR7123668A patent/FR2100841B1/fr not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0495776A4 (en) * | 1989-02-28 | 1992-02-10 | Us Secretary United States Dep | Stabilized nitric oxide-primary amine complexes useful as cardiovascular agents. |
EP0495776A1 (en) * | 1989-02-28 | 1992-07-29 | Us Health | Stabilized nitric oxide-primary amine complexes useful as cardiovascular agents. |
US5208233A (en) * | 1989-09-15 | 1993-05-04 | The United States Of America As Represented By The Department Of Health And Human Services | Anti-hypertensive compositions of secondary amine-nitric oxide adducts and use thereof |
Also Published As
Publication number | Publication date |
---|---|
FR2100841B1 (en) | 1975-10-31 |
CH560178A5 (en) | 1975-03-27 |
FR2100841A1 (en) | 1972-03-24 |
DE2131826A1 (en) | 1972-01-05 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |