SU510146A3 - Способ получени производныхфенилэтиламина - Google Patents
Способ получени производныхфенилэтиламинаInfo
- Publication number
- SU510146A3 SU510146A3 SU1749281A SU1749281A SU510146A3 SU 510146 A3 SU510146 A3 SU 510146A3 SU 1749281 A SU1749281 A SU 1749281A SU 1749281 A SU1749281 A SU 1749281A SU 510146 A3 SU510146 A3 SU 510146A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- water
- salt
- methanol
- amino
- dissolved
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 4
- 150000007925 phenylethylamine derivatives Chemical class 0.000 title claims 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 18
- 150000003839 salts Chemical class 0.000 claims 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 8
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 6
- 150000001875 compounds Chemical class 0.000 claims 4
- 229910052987 metal hydride Inorganic materials 0.000 claims 4
- 150000004681 metal hydrides Chemical class 0.000 claims 4
- 150000007524 organic acids Chemical class 0.000 claims 4
- 235000005985 organic acids Nutrition 0.000 claims 4
- 239000000047 product Substances 0.000 claims 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 3
- 239000000203 mixture Substances 0.000 claims 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 2
- 150000001298 alcohols Chemical class 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 239000003153 chemical reaction reagent Substances 0.000 claims 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 2
- 150000002148 esters Chemical class 0.000 claims 2
- 150000007522 mineralic acids Chemical class 0.000 claims 2
- 238000002360 preparation method Methods 0.000 claims 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims 2
- 229910000033 sodium borohydride Inorganic materials 0.000 claims 2
- 239000012279 sodium borohydride Substances 0.000 claims 2
- SDQHHIMPZYXBMS-UHFFFAOYSA-N 2-amino-3-(3,4-dichlorophenyl)propan-1-ol Chemical class OCC(N)CC1=CC=C(Cl)C(Cl)=C1 SDQHHIMPZYXBMS-UHFFFAOYSA-N 0.000 claims 1
- SDYWXFYBZPNOFX-UHFFFAOYSA-N 3,4-dichloroaniline Chemical compound NC1=CC=C(Cl)C(Cl)=C1 SDYWXFYBZPNOFX-UHFFFAOYSA-N 0.000 claims 1
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 claims 1
- GCBCWTWQAFLKJG-UHFFFAOYSA-N [3-(4-chlorophenyl)-1-methoxy-1-oxopropan-2-yl]azanium;chloride Chemical compound [Cl-].COC(=O)C([NH3+])CC1=CC=C(Cl)C=C1 GCBCWTWQAFLKJG-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 238000009835 boiling Methods 0.000 claims 1
- 230000000694 effects Effects 0.000 claims 1
- 239000000284 extract Substances 0.000 claims 1
- -1 methanol or ethanol Chemical compound 0.000 claims 1
- GBMDVOWEEQVZKZ-UHFFFAOYSA-N methanol;hydrate Chemical compound O.OC GBMDVOWEEQVZKZ-UHFFFAOYSA-N 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 239000003208 petroleum Substances 0.000 claims 1
- 230000000144 pharmacologic effect Effects 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 239000002244 precipitate Substances 0.000 claims 1
- 239000001294 propane Substances 0.000 claims 1
- 238000011084 recovery Methods 0.000 claims 1
- 239000011780 sodium chloride Substances 0.000 claims 1
- 229910052938 sodium sulfate Inorganic materials 0.000 claims 1
- 235000011152 sodium sulphate Nutrition 0.000 claims 1
- 239000011975 tartaric acid Substances 0.000 claims 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH231671A CH550136A (de) | 1971-02-17 | 1971-02-17 | Verfahren zur herstellung neuer phenylpropanolamine. |
| CH1861771A CH565136A5 (en) | 1971-12-21 | 1971-12-21 | 2-amino-3-(halo phenyl) - propanols - as anorexic agents and anti depressants |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU510146A3 true SU510146A3 (ru) | 1976-04-05 |
Family
ID=25690113
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1749281A SU510146A3 (ru) | 1971-02-17 | 1972-02-16 | Способ получени производныхфенилэтиламина |
Country Status (9)
| Country | Link |
|---|---|
| BE (1) | BE779402A (enExample) |
| DE (1) | DE2206961A1 (enExample) |
| ES (1) | ES399820A1 (enExample) |
| FR (1) | FR2125484B1 (enExample) |
| GB (1) | GB1377787A (enExample) |
| HU (1) | HU163932B (enExample) |
| NL (1) | NL7201809A (enExample) |
| PL (1) | PL83310B1 (enExample) |
| SU (1) | SU510146A3 (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4788010A (en) * | 1985-04-24 | 1988-11-29 | E. R. Squibb & Sons, Inc. | Amino substituted benzenepropanols |
| FR2593499B1 (fr) * | 1986-01-30 | 1988-08-12 | Jouveinal Sa | Aminoalcools, leur procede de preparation et leurs applications, notamment en therapeutique |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3062839A (en) * | 1959-06-11 | 1962-11-06 | American Home Prod | Dihydroxy-tertiary-butylamines |
-
1972
- 1972-02-05 ES ES399820A patent/ES399820A1/es not_active Expired
- 1972-02-11 NL NL7201809A patent/NL7201809A/xx unknown
- 1972-02-14 DE DE19722206961 patent/DE2206961A1/de active Pending
- 1972-02-15 HU HUSA002314 patent/HU163932B/hu unknown
- 1972-02-15 FR FR7205050A patent/FR2125484B1/fr not_active Expired
- 1972-02-15 GB GB692572A patent/GB1377787A/en not_active Expired
- 1972-02-15 BE BE779402A patent/BE779402A/xx unknown
- 1972-02-15 PL PL15350272A patent/PL83310B1/pl unknown
- 1972-02-16 SU SU1749281A patent/SU510146A3/ru active
Also Published As
| Publication number | Publication date |
|---|---|
| FR2125484A1 (enExample) | 1972-09-29 |
| DE2206961A1 (de) | 1972-08-31 |
| PL83310B1 (en) | 1975-12-31 |
| BE779402A (fr) | 1972-08-16 |
| FR2125484B1 (enExample) | 1975-04-25 |
| NL7201809A (enExample) | 1972-08-21 |
| HU163932B (enExample) | 1973-11-28 |
| ES399820A1 (es) | 1975-07-01 |
| GB1377787A (en) | 1974-12-18 |
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