BG50993A1 - 2, 3, 5- three substituted oxazolydines and process for their preparation - Google Patents
2, 3, 5- three substituted oxazolydines and process for their preparationInfo
- Publication number
- BG50993A1 BG50993A1 BG9354290A BG9354290A BG50993A1 BG 50993 A1 BG50993 A1 BG 50993A1 BG 9354290 A BG9354290 A BG 9354290A BG 9354290 A BG9354290 A BG 9354290A BG 50993 A1 BG50993 A1 BG 50993A1
- Authority
- BG
- Bulgaria
- Prior art keywords
- carbon atoms
- alkyl
- formula
- image
- oxazolydines
- Prior art date
Links
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000001414 amino alcohols Chemical class 0.000 abstract 2
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 abstract 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 1
- 208000001953 Hypotension Diseases 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 208000021822 hypotensive Diseases 0.000 abstract 1
- 230000001077 hypotensive effect Effects 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
These compounds may be used in medicine. They have a hypotensive and β-blocking action and a common formula<IMAGE>,where R is a cycloalkyl radical with 5 to 8 carbon atoms, R1 is alkyl with a branched chain, containing between 2 and 6 carbon atoms, and X is alkyl with 1 to 6 carbon atoms, with a straight or branched chain, phenyl or low phenyl alkyl. They are derived by interacting amino alcohols (with a formula),<IMAGE>and aldehydes (with a formula XCHO), in which R, R1 and X take the designated values, at a mol proportion of amino alcohol to aldehyde 1:2, in a medium of benzol.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BG9354290A BG50993A1 (en) | 1990-12-28 | 1990-12-28 | 2, 3, 5- three substituted oxazolydines and process for their preparation |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BG9354290A BG50993A1 (en) | 1990-12-28 | 1990-12-28 | 2, 3, 5- three substituted oxazolydines and process for their preparation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BG50993A1 true BG50993A1 (en) | 1993-01-15 |
Family
ID=3923439
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BG9354290A BG50993A1 (en) | 1990-12-28 | 1990-12-28 | 2, 3, 5- three substituted oxazolydines and process for their preparation |
Country Status (1)
| Country | Link |
|---|---|
| BG (1) | BG50993A1 (en) |
-
1990
- 1990-12-28 BG BG9354290A patent/BG50993A1/en unknown
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