SU517249A3 - Способ получени бензиламинов или их солей - Google Patents
Способ получени бензиламинов или их солейInfo
- Publication number
- SU517249A3 SU517249A3 SU2065437A SU2065437A SU517249A3 SU 517249 A3 SU517249 A3 SU 517249A3 SU 2065437 A SU2065437 A SU 2065437A SU 2065437 A SU2065437 A SU 2065437A SU 517249 A3 SU517249 A3 SU 517249A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- carbon atoms
- general formula
- hydrogen
- alcohol
- dibromo
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 14
- 150000003839 salts Chemical class 0.000 title claims 6
- 150000003939 benzylamines Chemical class 0.000 title claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 17
- 229910052739 hydrogen Inorganic materials 0.000 claims 12
- 239000001257 hydrogen Substances 0.000 claims 11
- 125000000217 alkyl group Chemical group 0.000 claims 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 6
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 claims 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 5
- 229910052794 bromium Inorganic materials 0.000 claims 5
- 125000004429 atom Chemical group 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 4
- 150000002431 hydrogen Chemical group 0.000 claims 4
- 239000000460 chlorine Chemical group 0.000 claims 3
- 229910052801 chlorine Inorganic materials 0.000 claims 3
- 230000003993 interaction Effects 0.000 claims 3
- 239000002904 solvent Substances 0.000 claims 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- 150000001412 amines Chemical class 0.000 claims 2
- 238000006243 chemical reaction Methods 0.000 claims 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims 2
- 238000002955 isolation Methods 0.000 claims 2
- 238000002844 melting Methods 0.000 claims 2
- 230000008018 melting Effects 0.000 claims 2
- -1 morpholino carbonylmethyl Chemical group 0.000 claims 2
- 238000002360 preparation method Methods 0.000 claims 2
- GELMWIVBBPAMIO-UHFFFAOYSA-N 2-methylbutan-2-amine Chemical compound CCC(C)(C)N GELMWIVBBPAMIO-UHFFFAOYSA-N 0.000 claims 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims 1
- 241001506071 Melanitta Species 0.000 claims 1
- XTUVJUMINZSXGF-UHFFFAOYSA-N N-methylcyclohexylamine Chemical compound CNC1CCCCC1 XTUVJUMINZSXGF-UHFFFAOYSA-N 0.000 claims 1
- PAMIQIKDUOTOBW-UHFFFAOYSA-N N-methylcyclohexylamine Natural products CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
- 241000218657 Picea Species 0.000 claims 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims 1
- SYKNUAWMBRIEKB-UHFFFAOYSA-N [Cl].[Br] Chemical group [Cl].[Br] SYKNUAWMBRIEKB-UHFFFAOYSA-N 0.000 claims 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 125000002252 acyl group Chemical group 0.000 claims 1
- 150000001335 aliphatic alkanes Chemical class 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000003710 aryl alkyl group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 238000002425 crystallisation Methods 0.000 claims 1
- 230000008025 crystallization Effects 0.000 claims 1
- 229960004698 dichlorobenzyl alcohol Drugs 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- PSLIMVZEAPALCD-UHFFFAOYSA-N ethanol;ethoxyethane Chemical compound CCO.CCOCC PSLIMVZEAPALCD-UHFFFAOYSA-N 0.000 claims 1
- 235000015110 jellies Nutrition 0.000 claims 1
- 239000008274 jelly Substances 0.000 claims 1
- FBBDOOHMGLLEGJ-UHFFFAOYSA-N methane;hydrochloride Chemical compound C.Cl FBBDOOHMGLLEGJ-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 239000011574 phosphorus Substances 0.000 claims 1
- 239000011780 sodium chloride Substances 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19732337932 DE2337932A1 (de) | 1972-10-23 | 1973-07-26 | Neue verfahren zur herstellung von benzylaminen |
| DE2346743A DE2346743C3 (de) | 1972-10-23 | 1973-09-17 | 2- oder 4-Hydroxy-3,5-dihalogenbenzylamine, deren physiologisch verträgliche Salze, Verfahren zu ihrer Herstellung und diese enthaltende Arzneimittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU517249A3 true SU517249A3 (ru) | 1976-06-05 |
Family
ID=25765548
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU2065437A SU517249A3 (ru) | 1973-07-26 | 1974-10-10 | Способ получени бензиламинов или их солей |
| SU2065405A SU514564A3 (ru) | 1973-07-26 | 1974-10-10 | Способ получени бензиламинов |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU2065405A SU514564A3 (ru) | 1973-07-26 | 1974-10-10 | Способ получени бензиламинов |
Country Status (5)
| Country | Link |
|---|---|
| AT (2) | ATA88475A (enExample) |
| BG (1) | BG22383A3 (enExample) |
| ES (2) | ES423977A1 (enExample) |
| PL (2) | PL91889B1 (enExample) |
| SU (2) | SU517249A3 (enExample) |
-
1973
- 1973-10-17 AT AT8847573A patent/ATA88475A/de not_active IP Right Cessation
- 1973-10-17 AT AT8857573A patent/ATA88575A/de not_active IP Right Cessation
- 1973-10-20 BG BG024799A patent/BG22383A3/xx unknown
- 1973-10-22 PL PL17668073A patent/PL91889B1/pl unknown
- 1973-10-22 PL PL17667973A patent/PL91888B1/pl unknown
-
1974
- 1974-03-06 ES ES423977A patent/ES423977A1/es not_active Expired
- 1974-03-16 ES ES423978A patent/ES423978A1/es not_active Expired
- 1974-10-10 SU SU2065437A patent/SU517249A3/ru active
- 1974-10-10 SU SU2065405A patent/SU514564A3/ru active
Also Published As
| Publication number | Publication date |
|---|---|
| ATA88475A (de) | 1975-07-15 |
| BG22383A3 (bg) | 1977-02-20 |
| SU514564A3 (ru) | 1976-05-15 |
| PL91888B1 (enExample) | 1977-03-31 |
| ATA88575A (de) | 1975-07-15 |
| ES423978A1 (es) | 1976-07-01 |
| PL91889B1 (enExample) | 1977-03-31 |
| ES423977A1 (es) | 1976-06-16 |
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