IE37419B1 - 5-(4-amino-3,5-dichlorophenyl)-3-t.-butyl-oxazolidines,methods for their preparation and compositions containing them - Google Patents
5-(4-amino-3,5-dichlorophenyl)-3-t.-butyl-oxazolidines,methods for their preparation and compositions containing themInfo
- Publication number
- IE37419B1 IE37419B1 IE439/73A IE43973A IE37419B1 IE 37419 B1 IE37419 B1 IE 37419B1 IE 439/73 A IE439/73 A IE 439/73A IE 43973 A IE43973 A IE 43973A IE 37419 B1 IE37419 B1 IE 37419B1
- Authority
- IE
- Ireland
- Prior art keywords
- amino
- oxazolidines
- compounds
- march
- aryl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 150000002431 hydrogen Chemical group 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 abstract 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 abstract 1
- YEEBZSXTYHJGIV-UHFFFAOYSA-N NC1=C(C=C(C=C1Cl)C1CNCO1)Cl Chemical class NC1=C(C=C(C=C1Cl)C1CNCO1)Cl YEEBZSXTYHJGIV-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 230000001813 broncholytic effect Effects 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000005504 styryl group Chemical group 0.000 abstract 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 (2)
| Publication Number | Publication Date |
|---|---|
| IE37419L IE37419L (en) | 1973-09-18 |
| IE37419B1 true IE37419B1 (en) | 1977-07-20 |
Family
ID=5839379
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IE439/73A IE37419B1 (en) | 1972-03-18 | 1973-03-16 | 5-(4-amino-3,5-dichlorophenyl)-3-t.-butyl-oxazolidines,methods for their preparation and compositions containing them |
Country Status (29)
| Country | Link |
|---|---|
| US (1) | US3896141A (enExample) |
| JP (1) | JPS5123504B2 (enExample) |
| KR (1) | KR780000135B1 (enExample) |
| AT (1) | AT321907B (enExample) |
| AU (1) | AU470947B2 (enExample) |
| BE (1) | BE796941A (enExample) |
| BG (1) | BG22825A3 (enExample) |
| CA (1) | CA996554A (enExample) |
| CH (1) | CH577491A5 (enExample) |
| CS (1) | CS179981B2 (enExample) |
| DD (1) | DD108276A5 (enExample) |
| DE (1) | DE2213271C3 (enExample) |
| DK (1) | DK133431C (enExample) |
| ES (1) | ES412734A1 (enExample) |
| FI (1) | FI55655C (enExample) |
| FR (1) | FR2181829B1 (enExample) |
| GB (1) | GB1386751A (enExample) |
| HU (1) | HU165157B (enExample) |
| IE (1) | IE37419B1 (enExample) |
| IL (1) | IL41795A (enExample) |
| NL (1) | NL173640C (enExample) |
| NO (1) | NO136977C (enExample) |
| PH (1) | PH9990A (enExample) |
| PL (1) | PL89285B1 (enExample) |
| RO (1) | RO62878A (enExample) |
| SE (1) | SE381660B (enExample) |
| SU (1) | SU468424A3 (enExample) |
| YU (1) | YU35008B (enExample) |
| ZA (1) | ZA731832B (enExample) |
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
Also Published As
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