SU468424A3 - "Способ получени производных оксазолидина - Google Patents
"Способ получени производных оксазолидинаInfo
- Publication number
- SU468424A3 SU468424A3 SU1893863A SU1893863A SU468424A3 SU 468424 A3 SU468424 A3 SU 468424A3 SU 1893863 A SU1893863 A SU 1893863A SU 1893863 A SU1893863 A SU 1893863A SU 468424 A3 SU468424 A3 SU 468424A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- amino
- tert
- dichlorophenyl
- reaction
- oxazolidine derivatives
- Prior art date
Links
- 229940053194 antiepileptics oxazolidine derivative Drugs 0.000 title description 3
- 238000000034 method Methods 0.000 title description 3
- 150000002917 oxazolidines Chemical class 0.000 title description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 14
- -1 alkenyl radical Chemical class 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 238000000354 decomposition reaction Methods 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 150000001299 aldehydes Chemical class 0.000 description 3
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- 125000000068 chlorophenyl group Chemical group 0.000 description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Substances OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 2
- 239000008098 formaldehyde solution Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- PXRKCOCTEMYUEG-UHFFFAOYSA-N 5-aminoisoindole-1,3-dione Chemical compound NC1=CC=C2C(=O)NC(=O)C2=C1 PXRKCOCTEMYUEG-UHFFFAOYSA-N 0.000 description 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N N-butylamine Natural products CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
- 241001585714 Nola Species 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/04—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19722213271 DE2213271C3 (de) | 1972-03-18 | 1972-03-18 | Neue oxazolidine |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU468424A3 true SU468424A3 (ru) | 1975-04-25 |
Family
ID=5839379
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1893863A SU468424A3 (ru) | 1972-03-18 | 1973-03-13 | "Способ получени производных оксазолидина |
Country Status (29)
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4754047A (en) * | 1979-08-16 | 1988-06-28 | American Cyanamid Company | Phenylethanolamine derivatives and acid addition salts thereof for enhancing the growth rate of meat-producing animals and/or improving the efficiency of feed utilization thereby |
| JPS57161479A (en) * | 1981-03-29 | 1982-10-05 | Kankiyou Souken Consultant Kk | Improvement in melting furnace with preheating column utilizing exhaust gas |
| US4603422A (en) * | 1984-09-26 | 1986-07-29 | The United States Of America As Represented By The Secretary Of The Navy | Long-lived laser dye |
| US5149821A (en) * | 1990-10-11 | 1992-09-22 | Pfizer Inc | Process and intermediates for optically active 3-formyltetrahydropyrans |
-
1972
- 1972-03-18 DE DE19722213271 patent/DE2213271C3/de not_active Expired
-
1973
- 1973-02-27 DD DD169086A patent/DD108276A5/xx unknown
- 1973-03-06 AT AT194673A patent/AT321907B/de not_active IP Right Cessation
- 1973-03-08 US US339389A patent/US3896141A/en not_active Expired - Lifetime
- 1973-03-09 PH PH14412*A patent/PH9990A/en unknown
- 1973-03-13 SU SU1893863A patent/SU468424A3/ru active
- 1973-03-14 CS CS7300001852A patent/CS179981B2/cs unknown
- 1973-03-14 CH CH373073A patent/CH577491A5/xx not_active IP Right Cessation
- 1973-03-15 JP JP48030473A patent/JPS5123504B2/ja not_active Expired
- 1973-03-15 YU YU693/73A patent/YU35008B/xx unknown
- 1973-03-15 SE SE7303640A patent/SE381660B/xx unknown
- 1973-03-16 BE BE128942A patent/BE796941A/xx not_active IP Right Cessation
- 1973-03-16 IL IL41795A patent/IL41795A/xx unknown
- 1973-03-16 AU AU53394/73A patent/AU470947B2/en not_active Expired
- 1973-03-16 IE IE439/73A patent/IE37419B1/xx unknown
- 1973-03-16 FI FI823/73A patent/FI55655C/fi active
- 1973-03-16 ES ES412734A patent/ES412734A1/es not_active Expired
- 1973-03-16 HU HUTO901A patent/HU165157B/hu unknown
- 1973-03-16 GB GB1284173A patent/GB1386751A/en not_active Expired
- 1973-03-16 CA CA166,241A patent/CA996554A/en not_active Expired
- 1973-03-16 BG BG023014A patent/BG22825A3/xx unknown
- 1973-03-16 FR FR7309578A patent/FR2181829B1/fr not_active Expired
- 1973-03-16 NO NO1060/73A patent/NO136977C/no unknown
- 1973-03-16 DK DK144673A patent/DK133431C/da not_active IP Right Cessation
- 1973-03-16 ZA ZA00731832A patent/ZA731832B/xx unknown
- 1973-03-16 NL NLAANVRAGE7303685,A patent/NL173640C/xx not_active IP Right Cessation
- 1973-03-17 KR KR7300430A patent/KR780000135B1/ko not_active Expired
- 1973-03-17 PL PL1973161336A patent/PL89285B1/pl unknown
- 1973-03-19 RO RO7300074211A patent/RO62878A/ro unknown
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