ES423362A1 - Procedimiento para la obtencion de derivados de 2-hidroxi-3aminopropano de actividad beta-receptora. - Google Patents
Procedimiento para la obtencion de derivados de 2-hidroxi-3aminopropano de actividad beta-receptora.Info
- Publication number
- ES423362A1 ES423362A1 ES423362A ES423362A ES423362A1 ES 423362 A1 ES423362 A1 ES 423362A1 ES 423362 A ES423362 A ES 423362A ES 423362 A ES423362 A ES 423362A ES 423362 A1 ES423362 A1 ES 423362A1
- Authority
- ES
- Spain
- Prior art keywords
- carbon atoms
- amino
- alkyl
- alkoxy
- case
- 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
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical class CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 title abstract 2
- 102000012740 beta Adrenergic Receptors Human genes 0.000 title abstract 2
- 108010079452 beta Adrenergic Receptors Proteins 0.000 title abstract 2
- 230000000694 effects Effects 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 46
- 125000004432 carbon atom Chemical group C* 0.000 abstract 44
- 125000002947 alkylene group Chemical group 0.000 abstract 18
- 125000003545 alkoxy group Chemical group 0.000 abstract 16
- 229910052736 halogen Inorganic materials 0.000 abstract 13
- 150000002367 halogens Chemical class 0.000 abstract 13
- 125000003342 alkenyl group Chemical group 0.000 abstract 11
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 9
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 9
- 125000004849 alkoxymethyl group Chemical group 0.000 abstract 7
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- 150000003839 salts Chemical class 0.000 abstract 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- 150000001204 N-oxides Chemical class 0.000 abstract 3
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 abstract 3
- 125000003282 alkyl amino group Chemical group 0.000 abstract 3
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 3
- 125000004414 alkyl thio group Chemical group 0.000 abstract 3
- 125000005237 alkyleneamino group Chemical group 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 2
- 125000005236 alkanoylamino group Chemical group 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 125000005242 carbamoyl alkyl group Chemical group 0.000 abstract 2
- 125000004181 carboxyalkyl group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 150000002431 hydrogen Chemical class 0.000 abstract 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000003373 pyrazinyl group Chemical group 0.000 abstract 2
- 125000002098 pyridazinyl group Chemical group 0.000 abstract 2
- 125000004076 pyridyl group Chemical group 0.000 abstract 2
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000001589 carboacyl group Chemical group 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- -1 cyano, hydroxy Chemical group 0.000 abstract 1
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 230000003287 optical effect Effects 0.000 abstract 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH244473A CH584209A5 (en) | 1973-02-20 | 1973-02-20 | 3-amino-2-hydroxypropoxy substd. diazines and pyridines - with beta-adrenergic blocking or stimulating activity |
| CH133674 | 1974-01-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES423362A1 true ES423362A1 (es) | 1976-10-16 |
Family
ID=25687380
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES423362A Expired ES423362A1 (es) | 1973-02-20 | 1974-02-18 | Procedimiento para la obtencion de derivados de 2-hidroxi-3aminopropano de actividad beta-receptora. |
Country Status (2)
| Country | Link |
|---|---|
| ES (1) | ES423362A1 (es) |
| YU (4) | YU37150B (es) |
-
1974
- 1974-02-18 ES ES423362A patent/ES423362A1/es not_active Expired
- 1974-02-19 YU YU43674A patent/YU37150B/xx unknown
-
1980
- 1980-06-12 YU YU156880A patent/YU156880A/xx unknown
- 1980-06-12 YU YU156780A patent/YU156780A/xx unknown
- 1980-06-12 YU YU156980A patent/YU156980A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU6572674A (en) | 1975-08-21 |
| YU156880A (en) | 1983-04-27 |
| YU37150B (en) | 1984-08-31 |
| YU43674A (en) | 1982-06-18 |
| YU156780A (en) | 1983-04-27 |
| YU156980A (en) | 1983-04-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES446083A1 (es) | Procedimiento para la obtencion de derivados del 2-hidroxi-3-aminopropano de actividad beta-receptora. | |
| RU2376287C2 (ru) | Производные бензамида, способ их получения и их применение, фармацевтическая композиция и способ обеспечения ингибирующего действия по отношению к hdac | |
| DE3065489D1 (en) | (piperidinylalkyl)quinazoline derivatives, process for their preparation and pharmaceutical compositions containing them | |
| KR960004344A (ko) | 6원 질소 함유 헤테로아릴-옥사졸리디논 | |
| ES8302783A1 (es) | "un procedimiento para preparar un compuesto de inclusion de ciclodextrina". | |
| ES405942A1 (es) | Procedimiento para la preparacion de 2-fenilimino-imidazo- lidinas. | |
| ES447150A1 (es) | Un procedimiento para la preparacion de un compuesto de pi- perazinilpipazina. | |
| ES423362A1 (es) | Procedimiento para la obtencion de derivados de 2-hidroxi-3aminopropano de actividad beta-receptora. | |
| AR240828A2 (es) | Procedimiento para obtener nuevos derivados de 1h,3h-pirrolo[1,2-c!tiazol y sus sales | |
| ES516554A0 (es) | Procedimiento para preparar nuevos derivados de etenilimidazol. | |
| ES425216A1 (es) | Procedimiento para la preparacion de nuevas triazolo - 1,5 - benzodiazepinas sustituidas. | |
| ES475131A1 (es) | Procedimiento para la preparacion de derivados 1,4-benzodia-zepinicos | |
| ES446082A1 (es) | Procedimiento para la obtencion de derivados de 1-pirazini- loxi-2-hidroxi-3-aminopropano. | |
| ATE18763T1 (de) | Diazolyl-alkanole, verfahren zu ihrer herstellung und ihre verwendung als antimykotische mittel. | |
| GB1193917A (en) | Improvements in or relating to Heterocyclic Compounds and the Manufacture Thereof | |
| FR2267102A1 (en) | 2,6-Di(branched alkylamino)pyridines - for treatment of fatty degeneration and diabetes | |
| ES8300776A1 (es) | Procedimiento para la obtencion de nuevos derivados de la tiazolo (3,2-a)pirimidina | |
| ES407816A1 (es) | Metodo para producir derivados de benzodiazepina. | |
| GB1158632A (en) | New Tri- and Tetrathiophosphate Esters | |
| ES8205414A1 (es) | Un procedimiento de preparacion de derivados de tiazol | |
| ES8103748A1 (es) | Procedimiento para la preparacion de 5,6,7,8-tetrahidropira-zolo (3,4-b)(1,5) diazepin-1h,4h-5,7-dionas | |
| ES383390A1 (es) | Procedimiento para la preparacion de derivados de la dihi- dro - 10,11 dibenzo (b,f) azepina. | |
| ES303109A1 (es) | Procedimiento para la preparacion de imidazo quinazolinas y pirimido quinazolinas. | |
| PT82416A (de) | Mehrfach substituierte pyridin-1-oxide verfahren zu ihrer herstellung die sie enthaltenden arzneimittel und ihre verwendung | |
| ES387137A1 (es) | Un procedimiento para la preparacion de nuevas tetrahidro-1,5-benzodiazepin-4-onas. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FD1A | Patent lapsed |
Effective date: 19840402 |