GB1272974A - 02-SUBSTITUTED-11,12-DIHYDRO-6H-DIBENZ [b,f][1,4] OXAZOCINES - Google Patents
02-SUBSTITUTED-11,12-DIHYDRO-6H-DIBENZ [b,f][1,4] OXAZOCINESInfo
- Publication number
- GB1272974A GB1272974A GB2199369A GB2199369A GB1272974A GB 1272974 A GB1272974 A GB 1272974A GB 2199369 A GB2199369 A GB 2199369A GB 2199369 A GB2199369 A GB 2199369A GB 1272974 A GB1272974 A GB 1272974A
- Authority
- GB
- United Kingdom
- Prior art keywords
- compound
- afford
- alkyl
- substituted
- halide
- 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
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 6
- 150000001875 compounds Chemical class 0.000 abstract 5
- -1 12 - Substituted 11,12 - dihydro- 6H -dibenz[b,f][1,4]oxazocines Chemical class 0.000 abstract 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- 150000001412 amines Chemical class 0.000 abstract 3
- 229910021529 ammonia Inorganic materials 0.000 abstract 3
- 230000003993 interaction Effects 0.000 abstract 3
- 239000012280 lithium aluminium hydride Substances 0.000 abstract 3
- 229910000033 sodium borohydride Inorganic materials 0.000 abstract 3
- 239000012279 sodium borohydride Substances 0.000 abstract 3
- FCSKOFQQCWLGMV-UHFFFAOYSA-N 5-{5-[2-chloro-4-(4,5-dihydro-1,3-oxazol-2-yl)phenoxy]pentyl}-3-methylisoxazole Chemical compound O1N=C(C)C=C1CCCCCOC1=CC=C(C=2OCCN=2)C=C1Cl FCSKOFQQCWLGMV-UHFFFAOYSA-N 0.000 abstract 2
- FKLJPTJMIBLJAV-UHFFFAOYSA-N Compound IV Chemical compound O1N=C(C)C=C1CCCCCCCOC1=CC=C(C=2OCCN=2)C=C1 FKLJPTJMIBLJAV-UHFFFAOYSA-N 0.000 abstract 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 239000000010 aprotic solvent Substances 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- VDWGTBWAWJNNQM-UHFFFAOYSA-N 2-[(2-aminophenoxy)methyl]benzoic acid Chemical compound NC1=CC=CC=C1OCC1=CC=CC=C1C(O)=O VDWGTBWAWJNNQM-UHFFFAOYSA-N 0.000 abstract 1
- DRSHXJFUUPIBHX-UHFFFAOYSA-N COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 Chemical compound COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 DRSHXJFUUPIBHX-UHFFFAOYSA-N 0.000 abstract 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 206010020751 Hypersensitivity Diseases 0.000 abstract 1
- 239000005991 Sodium o-nitrophenolate Substances 0.000 abstract 1
- GUGOEEXESWIERI-UHFFFAOYSA-N Terfenadine Chemical compound C1=CC(C(C)(C)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 GUGOEEXESWIERI-UHFFFAOYSA-N 0.000 abstract 1
- 206010047281 Ventricular arrhythmia Diseases 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 150000001266 acyl halides Chemical class 0.000 abstract 1
- 239000003513 alkali Substances 0.000 abstract 1
- 150000001342 alkaline earth metals Chemical class 0.000 abstract 1
- 230000029936 alkylation Effects 0.000 abstract 1
- 238000005804 alkylation reaction Methods 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 230000007815 allergy Effects 0.000 abstract 1
- 230000001387 anti-histamine Effects 0.000 abstract 1
- 239000000739 antihistaminic agent Substances 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- AAHZCIWUDPKSJP-UHFFFAOYSA-N methyl 2-(chloromethyl)benzoate Chemical compound COC(=O)C1=CC=CC=C1CCl AAHZCIWUDPKSJP-UHFFFAOYSA-N 0.000 abstract 1
- 150000004702 methyl esters Chemical class 0.000 abstract 1
- 150000002828 nitro derivatives Chemical class 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 238000007363 ring formation reaction Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- AXKBOWBNOCUNJL-UHFFFAOYSA-M sodium;2-nitrophenolate Chemical compound [Na+].[O-]C1=CC=CC=C1[N+]([O-])=O AXKBOWBNOCUNJL-UHFFFAOYSA-M 0.000 abstract 1
- 125000004951 trihalomethoxy group Chemical group 0.000 abstract 1
- 125000004953 trihalomethyl group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D267/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D267/22—Eight-membered rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US72990268A | 1968-05-17 | 1968-05-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1272974A true GB1272974A (en) | 1972-05-03 |
Family
ID=24933083
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2199369A Expired GB1272974A (en) | 1968-05-17 | 1969-04-30 | 02-SUBSTITUTED-11,12-DIHYDRO-6H-DIBENZ [b,f][1,4] OXAZOCINES |
Country Status (4)
| Country | Link |
|---|---|
| CH (1) | CH514617A (enExample) |
| DE (1) | DE1923965A1 (enExample) |
| FR (1) | FR2008758A1 (enExample) |
| GB (1) | GB1272974A (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005040314A3 (en) * | 2003-10-17 | 2005-07-21 | Gillette Co | Fuel composition in fuel cartridges for dmfcs |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE616983A (enExample) * | 1961-04-27 |
-
1969
- 1969-04-30 GB GB2199369A patent/GB1272974A/en not_active Expired
- 1969-05-10 DE DE19691923965 patent/DE1923965A1/de active Pending
- 1969-05-14 CH CH738069A patent/CH514617A/de not_active IP Right Cessation
- 1969-05-14 FR FR6915759A patent/FR2008758A1/fr not_active Withdrawn
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005040314A3 (en) * | 2003-10-17 | 2005-07-21 | Gillette Co | Fuel composition in fuel cartridges for dmfcs |
| US7314493B2 (en) | 2003-10-17 | 2008-01-01 | The Gillette Company | Fuel composition in fuel cartridges for DMFCs |
Also Published As
| Publication number | Publication date |
|---|---|
| CH514617A (de) | 1971-10-31 |
| DE1923965A1 (de) | 1969-11-27 |
| FR2008758A1 (enExample) | 1970-01-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES8107185A1 (es) | Procedimiento para preparar piperidinas y pirrolidinas sus- tituidas | |
| DE3362784D1 (en) | Process for preparing free-flowing ethylcellulose microcapsules | |
| GB1087242A (en) | Improvements in or relating to naphthalene derivatives and the manufacture thereof | |
| ES420630A1 (es) | Procedimiento para la preparacion de n-(furil-metil)-morfi-nanos. | |
| ES457001A1 (es) | Un procedimiento de preparacion de derivados de fenetilamina. | |
| GB1173227A (en) | Amino-Isoquinolines | |
| GB1272974A (en) | 02-SUBSTITUTED-11,12-DIHYDRO-6H-DIBENZ [b,f][1,4] OXAZOCINES | |
| GB1043510A (en) | D-(--)-n-alkyl-1-phenyl-2-aminoethanols | |
| Marshall et al. | The Synthesis of Alkenes via Reduction-Elimination of 1, 2-Diol Cyclic Phosphate Derivatives | |
| ES8104241A1 (es) | Un procedimiento para la preparacion de compuestos derivadosde 1-((naftil substituido)etil)imidazol | |
| GB1265631A (enExample) | ||
| ES338709A1 (es) | Un procedimiento de preparar derivados de isoquinoleina. | |
| ES405479A1 (es) | Un procedimiento para la preparacion de derivados de benzo-diacepina. | |
| GB997637A (en) | Substituted 2-cyclopropylmethyl-6,7-benzmorphans | |
| ES397453A1 (es) | Procedimiento para la preparacion de derivados de imidazo- lina. | |
| ES461758A1 (es) | Nuevo procedimiento de obtencion de derivados tiocromanicos. | |
| GB1181295A (en) | Improvements in or relating to Naphthalene Derivatives and the Manufacture Thereof | |
| GB1063572A (en) | A process for preparing new triamcinolone esters | |
| GB1387783A (en) | Thiophene derivatives, method for their preparation and pharmaceutical composition thereof | |
| JPS5283436A (en) | Preparation of intermediates for synthesis of prostaglandin | |
| JPS51113882A (en) | Method for preparing 1-(alpha -alkoxyalkyl)-uracil derivatives | |
| JPS5479201A (en) | Preparation of aldehydes | |
| GB1141530A (en) | Salicylic acid derivatives | |
| GB1193521A (en) | Novel Esters of 1-Phenyl-1-Benzyl-2-Methyl-3-Dimethylaminopropanol, the preparation thereof and Compositions containing the same | |
| GB1197707A (en) | Diarylacylophenones and Process for their Preparation |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |