ES8401473A1 - Procedimiento para la preparacion de derivados de benzazepina. - Google Patents
Procedimiento para la preparacion de derivados de benzazepina.Info
- Publication number
- ES8401473A1 ES8401473A1 ES517759A ES517759A ES8401473A1 ES 8401473 A1 ES8401473 A1 ES 8401473A1 ES 517759 A ES517759 A ES 517759A ES 517759 A ES517759 A ES 517759A ES 8401473 A1 ES8401473 A1 ES 8401473A1
- Authority
- ES
- Spain
- Prior art keywords
- group
- alkyl
- carbon atoms
- hydroxy
- alkoxy
- 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
- 150000008038 benzoazepines Chemical class 0.000 title abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 50
- 125000004432 carbon atom Chemical group C* 0.000 abstract 31
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 19
- 125000003545 alkoxy group Chemical group 0.000 abstract 17
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 11
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical group CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 abstract 10
- 125000005530 alkylenedioxy group Chemical group 0.000 abstract 10
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 9
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 7
- 239000005977 Ethylene Substances 0.000 abstract 7
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 7
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 abstract 6
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 abstract 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 5
- 125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 abstract 5
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 5
- 125000005843 halogen group Chemical group 0.000 abstract 5
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 abstract 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 5
- -1 CH:CH Chemical group 0.000 abstract 4
- 125000002252 acyl group Chemical group 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 150000003839 salts Chemical class 0.000 abstract 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- 125000005236 alkanoylamino group Chemical group 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 3
- 125000003282 alkyl amino group Chemical group 0.000 abstract 3
- 125000001589 carboacyl group Chemical group 0.000 abstract 3
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 3
- 125000002071 phenylalkoxy group Chemical group 0.000 abstract 3
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 3
- DQFQCHIDRBIESA-UHFFFAOYSA-N 1-benzazepine Chemical compound N1C=CC=CC2=CC=CC=C12 DQFQCHIDRBIESA-UHFFFAOYSA-N 0.000 abstract 2
- 241000699670 Mus sp. Species 0.000 abstract 2
- 208000007888 Sinus Tachycardia Diseases 0.000 abstract 2
- 125000003277 amino group Chemical group 0.000 abstract 2
- 230000001022 anti-muscarinic effect Effects 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 230000000694 effects Effects 0.000 abstract 2
- CCGKOQOJPYTBIH-UHFFFAOYSA-N ethenone Chemical compound C=C=O CCGKOQOJPYTBIH-UHFFFAOYSA-N 0.000 abstract 2
- 208000019622 heart disease Diseases 0.000 abstract 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 2
- 238000001990 intravenous administration Methods 0.000 abstract 2
- 230000000302 ischemic effect Effects 0.000 abstract 2
- 230000005923 long-lasting effect Effects 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 1
- 150000007522 mineralic acids Chemical class 0.000 abstract 1
- 150000007524 organic acids Chemical class 0.000 abstract 1
- 235000005985 organic acids Nutrition 0.000 abstract 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
PROCEDIMIENTO PARA LA OBTENCION DE DERIVADOS DE BENZAZEPINA Y DE SUS SALES DE ADICION DE ACIDOS FISIOLOGICAMENTE COMPATIBLES, DE FORMULA (I), EN LA QUE A, B, E, G, R1, R2, R3, R4, R5 Y R6 PUEDEN SER VARIOS TIPOS DE RADICALES.CONSISTE EN LA REACCION DE HALOGENACION DE UN COMPUESTO DE FORMULA (II), EN LA QUE TODOS LOS SIMBOLOS TIENEN EL MISMO SIGNIFICADO QUE EN LA FORMULA (I); SEGUIDA DE LA EVENTUAL TRANSFORMACION DEL PRODUCTO OBTENIDO EN LAS SALES CON ACIDOS. LA HALOGENACION SE EFECTUA EN UN DISOLVENTE INERTE, CON UN HALOGENO O UN DERIVADO HALOGENADO ADECUADO, ATEMPERATURAS ENTRE 0JC Y 50JC.ESTOS COMPUESTOS TIENEN APLICACIONES FARMACOLOGICAS PARA EL TRATAMIENTO DE TAQUICARDIAS SINUSALES Y DE ENFERMEDADES CARDIACAS ISQUEMICAS.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES517759A ES517759A0 (es) | 1982-11-29 | 1982-11-29 | Procedimiento para la preparacion de derivados de benzazepina. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES517759A ES517759A0 (es) | 1982-11-29 | 1982-11-29 | Procedimiento para la preparacion de derivados de benzazepina. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| ES8401473A1 true ES8401473A1 (es) | 1983-12-16 |
| ES517759A0 ES517759A0 (es) | 1983-12-16 |
Family
ID=8484992
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES517759A Granted ES517759A0 (es) | 1982-11-29 | 1982-11-29 | Procedimiento para la preparacion de derivados de benzazepina. |
Country Status (1)
| Country | Link |
|---|---|
| ES (1) | ES517759A0 (es) |
-
1982
- 1982-11-29 ES ES517759A patent/ES517759A0/es active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| ES517759A0 (es) | 1983-12-16 |
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