GB1153647A - 2-Anilino Benzoxazole Basic Ethers - Google Patents
2-Anilino Benzoxazole Basic EthersInfo
- Publication number
- GB1153647A GB1153647A GB02843/67A GB1284367A GB1153647A GB 1153647 A GB1153647 A GB 1153647A GB 02843/67 A GB02843/67 A GB 02843/67A GB 1284367 A GB1284367 A GB 1284367A GB 1153647 A GB1153647 A GB 1153647A
- Authority
- GB
- United Kingdom
- Prior art keywords
- benzoxazole
- anilino
- aniline
- chloroethoxy
- mercapto
- 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
- 150000002170 ethers Chemical class 0.000 title 1
- BFLIOKCEGCUTNH-UHFFFAOYSA-N n-phenyl-1,3-benzoxazol-2-amine Chemical compound N=1C2=CC=CC=C2OC=1NC1=CC=CC=C1 BFLIOKCEGCUTNH-UHFFFAOYSA-N 0.000 title 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 5
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical class C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- DNXIKVLOVZVMQF-UHFFFAOYSA-N (3beta,16beta,17alpha,18beta,20alpha)-17-hydroxy-11-methoxy-18-[(3,4,5-trimethoxybenzoyl)oxy]-yohimban-16-carboxylic acid, methyl ester Natural products C1C2CN3CCC(C4=CC=C(OC)C=C4N4)=C4C3CC2C(C(=O)OC)C(O)C1OC(=O)C1=CC(OC)=C(OC)C(OC)=C1 DNXIKVLOVZVMQF-UHFFFAOYSA-N 0.000 abstract 1
- KWTSXDURSIMDCE-QMMMGPOBSA-N (S)-amphetamine Chemical compound C[C@H](N)CC1=CC=CC=C1 KWTSXDURSIMDCE-QMMMGPOBSA-N 0.000 abstract 1
- NUMDWMDMUXZMHA-UHFFFAOYSA-N 6-methyl-3h-1,3-benzoxazole-2-thione Chemical compound CC1=CC=C2NC(=S)OC2=C1 NUMDWMDMUXZMHA-UHFFFAOYSA-N 0.000 abstract 1
- 229940121948 Muscarinic receptor antagonist Drugs 0.000 abstract 1
- LCQMZZCPPSWADO-UHFFFAOYSA-N Reserpilin Natural products COC(=O)C1COCC2CN3CCc4c([nH]c5cc(OC)c(OC)cc45)C3CC12 LCQMZZCPPSWADO-UHFFFAOYSA-N 0.000 abstract 1
- QEVHRUUCFGRFIF-SFWBKIHZSA-N Reserpine Natural products O=C(OC)[C@@H]1[C@H](OC)[C@H](OC(=O)c2cc(OC)c(OC)c(OC)c2)C[C@H]2[C@@H]1C[C@H]1N(C2)CCc2c3c([nH]c12)cc(OC)cc3 QEVHRUUCFGRFIF-SFWBKIHZSA-N 0.000 abstract 1
- 229940025084 amphetamine Drugs 0.000 abstract 1
- 150000001448 anilines Chemical class 0.000 abstract 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 229940125681 anticonvulsant agent Drugs 0.000 abstract 1
- 239000001961 anticonvulsive agent Substances 0.000 abstract 1
- 239000000935 antidepressant agent Substances 0.000 abstract 1
- 229940005513 antidepressants Drugs 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 239000000812 cholinergic antagonist Substances 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 230000003389 potentiating effect Effects 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- BJOIZNZVOZKDIG-MDEJGZGSSA-N reserpine Chemical compound O([C@H]1[C@@H]([C@H]([C@H]2C[C@@H]3C4=C([C]5C=CC(OC)=CC5=N4)CCN3C[C@H]2C1)C(=O)OC)OC)C(=O)C1=CC(OC)=C(OC)C(OC)=C1 BJOIZNZVOZKDIG-MDEJGZGSSA-N 0.000 abstract 1
- 229960003147 reserpine Drugs 0.000 abstract 1
- MDMGHDFNKNZPAU-UHFFFAOYSA-N roserpine Natural products C1C2CN3CCC(C4=CC=C(OC)C=C4N4)=C4C3CC2C(OC(C)=O)C(OC)C1OC(=O)C1=CC(OC)=C(OC)C(OC)=C1 MDMGHDFNKNZPAU-UHFFFAOYSA-N 0.000 abstract 1
- 125000000467 secondary amino group Chemical class [H]N([*:1])[*:2] 0.000 abstract 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 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
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
- C07D263/58—Benzoxazoles; Hydrogenated benzoxazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
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)
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB02843/67A GB1153647A (en) | 1967-03-20 | 1967-03-20 | 2-Anilino Benzoxazole Basic Ethers |
| US711866A US3594373A (en) | 1967-03-20 | 1968-03-11 | Bases of 2-anilinobenzoxazoles and process for making them |
| FR1556798D FR1556798A (https=) | 1967-03-20 | 1968-03-19 | |
| BE712475D BE712475A (https=) | 1967-03-20 | 1968-03-20 | |
| SE3670/68A SE323378B (https=) | 1967-03-20 | 1968-03-20 | |
| DE19681770005 DE1770005A1 (de) | 1967-03-20 | 1968-03-20 | Substituierte Anilinbenzoxazole |
| NL6803959A NL6803959A (https=) | 1967-03-20 | 1968-03-20 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB02843/67A GB1153647A (en) | 1967-03-20 | 1967-03-20 | 2-Anilino Benzoxazole Basic Ethers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1153647A true GB1153647A (en) | 1969-05-29 |
Family
ID=10012151
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB02843/67A Expired GB1153647A (en) | 1967-03-20 | 1967-03-20 | 2-Anilino Benzoxazole Basic Ethers |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3594373A (https=) |
| BE (1) | BE712475A (https=) |
| DE (1) | DE1770005A1 (https=) |
| FR (1) | FR1556798A (https=) |
| GB (1) | GB1153647A (https=) |
| NL (1) | NL6803959A (https=) |
| SE (1) | SE323378B (https=) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4275210A (en) * | 1971-05-04 | 1981-06-23 | Eli Lilly And Company | Substituted 2-anilinobenzoxazoles |
| US4314065A (en) | 1979-03-19 | 1982-02-02 | Ici Australia Limited | Phenylamine substituted on amine with a benzo(oxa, thia or di) azole group |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4594425A (en) * | 1984-02-09 | 1986-06-10 | American Home Products Corporation | Heterocyclic compounds as antiallergic agents |
-
1967
- 1967-03-20 GB GB02843/67A patent/GB1153647A/en not_active Expired
-
1968
- 1968-03-11 US US711866A patent/US3594373A/en not_active Expired - Lifetime
- 1968-03-19 FR FR1556798D patent/FR1556798A/fr not_active Expired
- 1968-03-20 SE SE3670/68A patent/SE323378B/xx unknown
- 1968-03-20 BE BE712475D patent/BE712475A/xx unknown
- 1968-03-20 DE DE19681770005 patent/DE1770005A1/de active Pending
- 1968-03-20 NL NL6803959A patent/NL6803959A/xx unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4275210A (en) * | 1971-05-04 | 1981-06-23 | Eli Lilly And Company | Substituted 2-anilinobenzoxazoles |
| US4314065A (en) | 1979-03-19 | 1982-02-02 | Ici Australia Limited | Phenylamine substituted on amine with a benzo(oxa, thia or di) azole group |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1770005A1 (de) | 1971-09-16 |
| BE712475A (https=) | 1968-07-31 |
| NL6803959A (https=) | 1968-09-23 |
| FR1556798A (https=) | 1969-02-07 |
| SE323378B (https=) | 1970-05-04 |
| US3594373A (en) | 1971-07-20 |
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