NO133801B - - Google Patents
Download PDFInfo
- Publication number
- NO133801B NO133801B NO1612/68A NO161268A NO133801B NO 133801 B NO133801 B NO 133801B NO 1612/68 A NO1612/68 A NO 1612/68A NO 161268 A NO161268 A NO 161268A NO 133801 B NO133801 B NO 133801B
- Authority
- NO
- Norway
- Prior art keywords
- lower alkyl
- alkyl radicals
- general formula
- denote
- compounds
- Prior art date
Links
- -1 1-piperidyl Chemical group 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 7
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- 239000007858 starting material Substances 0.000 claims description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 150000008508 dibenzocycloheptenes Chemical class 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 15
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 5
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 4
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000001953 recrystallisation Methods 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- UQSQSQZYBQSBJZ-UHFFFAOYSA-N fluorosulfonic acid Chemical compound OS(F)(=O)=O UQSQSQZYBQSBJZ-UHFFFAOYSA-N 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 2
- SFHGZGMYSAGHBK-UHFFFAOYSA-N 2-bromo-11-oxo-5,6-dihydrodibenzo[3,1-b:3',1'-f][7]annulene-9-sulfonyl fluoride Chemical compound C1CC2=CC=C(Br)C=C2C(=O)C2=CC(S(=O)(=O)F)=CC=C21 SFHGZGMYSAGHBK-UHFFFAOYSA-N 0.000 description 1
- HYKKSGGCBKGVQG-UHFFFAOYSA-N 2-bromo-5,6-dihydrodibenzo[3,1-[7]annulen-11-one Chemical compound C1CC2=CC=CC=C2C(=O)C2=CC(Br)=CC=C21 HYKKSGGCBKGVQG-UHFFFAOYSA-N 0.000 description 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 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000001430 anti-depressive effect Effects 0.000 description 1
- 230000001387 anti-histamine Effects 0.000 description 1
- 239000000739 antihistaminic agent Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000001624 sedative effect Effects 0.000 description 1
- 239000011775 sodium fluoride Substances 0.000 description 1
- 235000013024 sodium fluoride Nutrition 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NO1612/68A NO133801C (enrdf_load_html_response) | 1962-09-24 | 1968-04-26 |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US225864A US3306934A (en) | 1962-09-24 | 1962-09-24 | 5-(aminopropylidene)-and 5-hydroxy-5-(aminopropyl)-3-dialkylsulfamoyl-5h-dibenzo[a,d] cycloheptenes |
| NO150187A NO115799B (enrdf_load_html_response) | 1962-09-24 | 1963-09-21 | |
| NO1612/68A NO133801C (enrdf_load_html_response) | 1962-09-24 | 1968-04-26 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO133801B true NO133801B (enrdf_load_html_response) | 1976-03-22 |
| NO133801C NO133801C (enrdf_load_html_response) | 1976-06-30 |
Family
ID=27352564
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO1612/68A NO133801C (enrdf_load_html_response) | 1962-09-24 | 1968-04-26 |
Country Status (1)
| Country | Link |
|---|---|
| NO (1) | NO133801C (enrdf_load_html_response) |
-
1968
- 1968-04-26 NO NO1612/68A patent/NO133801C/no unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NO133801C (enrdf_load_html_response) | 1976-06-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CH650245A5 (de) | Substituierte propanolamin- und morpholinderivate und verfahren zu deren herstellung. | |
| DE2711655C2 (enrdf_load_html_response) | ||
| DE2716943A1 (de) | Organische verbindungen, ihre verwendung und herstellung | |
| US2768207A (en) | Unitary process for the production of 2-benzylphenyl beta-dimethylaminoethyl ether dihydrogen citrate | |
| NO133801B (enrdf_load_html_response) | ||
| CH631454A5 (de) | Verfahren zur herstellung von basisch substituierten xanthinderivaten. | |
| DE3424586A1 (de) | 3-aminocarbonylmethoxy-5-phenyl-pyrazol-verbindungen sowie verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel | |
| US4020104A (en) | Process for isomerizing cis,cis- and cis,trans-isomers of di-(p-aminocyclohexyl)methane to the corresponding trans,trans-isomer | |
| US3042684A (en) | J-ethtl-jj-nitrovinylindole | |
| EP0024560B1 (de) | Neue 3-Amino-1-benzoxepin-Derivate und ihre Salze; Verfahren zu deren Herstellung und diese Verbindungen enthaltende Arzneimittel | |
| PL84351B1 (enrdf_load_html_response) | ||
| EP0025501B1 (de) | Neue N-Aminoalkylindol-Derivate und ihre Salze; Verfahren zu deren Herstellung und diese Verbindungen enthaltende Arzneimittel | |
| DE3300522A1 (de) | 3,3-dialkyl- und 3,3-alkylen-indolinderivate, verfahren zu ihrer herstellung und pharmazeutische praeparate sie enthaltend | |
| DE2121996C3 (de) | Dibasische Äther des 2,6- und 2,7-Dihydroxyanthrachinons der Herstellung und pharmazeutische Zubereitung | |
| US3504031A (en) | 1-aminoalkyl-1-phenylindene process and intermediate therefor | |
| AT259553B (de) | Verfahren zur Herstellung von Indolderivaten | |
| DE2711656A1 (de) | Neue pyridin-3-ole | |
| NO144099B (no) | Dyse for maskinell flammehoevling av enkelte defekter paa overflaten til et metallegeme | |
| DE1620724A1 (de) | Naphthoxasinone und Verfahren zu ihrer Herstellung | |
| DE1802208A1 (de) | Verfahren zur Herstellung salidiuretisch wirksamer Sulfamylanthranilsaeuren | |
| CH634559A5 (de) | Verfahren zur herstellung von 3-halogen-3-kohlenwasserstoffthio-oxindolen und verfahren zur herstellung von isatinen. | |
| AT239241B (de) | Verfahren zur Herstellung von neuen Thiaxanthenderivaten | |
| SU1049474A1 (ru) | Способ получени @ -(3-фенилаллил) бензамидов | |
| AT376964B (de) | Verfahren zum herstellen von neuen substituierten morpholinderivaten und von deren isomeren und salzen | |
| AT226692B (de) | Verfahren zur Herstellung von neuen α-Pyrrolidino-valerophenonen |