DE287959C - - Google Patents
Info
- Publication number
- DE287959C DE287959C DENDAT287959D DE287959DA DE287959C DE 287959 C DE287959 C DE 287959C DE NDAT287959 D DENDAT287959 D DE NDAT287959D DE 287959D A DE287959D A DE 287959DA DE 287959 C DE287959 C DE 287959C
- Authority
- DE
- Germany
- Prior art keywords
- phenylquinoline
- isoamyl
- carboxylic acid
- ester
- derivatives
- 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.)
- Active
Links
- YTRMTPPVNRALON-UHFFFAOYSA-N 2-phenyl-4-quinolinecarboxylic acid Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=CC=C1 YTRMTPPVNRALON-UHFFFAOYSA-N 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 2
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims 1
- 238000007796 conventional method Methods 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- -1 isoamyl ester Chemical class 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- CZHLPWNZCJEPJB-UHFFFAOYSA-N 1-chloro-3-methylbutane Chemical compound CC(C)CCCl CZHLPWNZCJEPJB-UHFFFAOYSA-N 0.000 description 1
- SQCZQTSHSZLZIQ-UHFFFAOYSA-N 1-chloropentane Chemical compound CCCCCCl SQCZQTSHSZLZIQ-UHFFFAOYSA-N 0.000 description 1
- ASHDEYOBUFZOND-UHFFFAOYSA-N 8-methoxy-2-phenylquinoline-4-carboxylic acid Chemical compound N1=C2C(OC)=CC=CC2=C(C(O)=O)C=C1C1=CC=CC=C1 ASHDEYOBUFZOND-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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 to ring carbon atoms
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D215/50—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 4
- C07D215/52—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 4 with aryl radicals attached in position 2
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE287959C true DE287959C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
Family
ID=543132
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT287959D Active DE287959C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE287959C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
-
0
- DE DENDAT287959D patent/DE287959C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE287959C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| DE1593315C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| DE1793693B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| DE2124904C3 (de) | Hydroxy- und Alkoxyacetamido-trijodbenzoesäuren, deren Salze mit physiologisch verträglichen Basen, Verfahren zu deren Herstellung und diese Verbindungen enthaltende Röntgenkontrastmittel | |
| DE1082598B (de) | Verfahren zur Herstellung von ª‡-Keto-2, 3, 4, 5-tetrahydro-ª‰-carbolinen | |
| DE825684C (de) | Verfahren zur Herstellung von Carbonsaeureestern | |
| DE1593315B1 (de) | 9-Isopropyliden-9,10-dihydroanthracen-10-carbonsaeure-ss-diaethylamino-aethylester,deren Salze und Verfahren zu deren Herstellung | |
| DE348484C (de) | Verfahren zur Darstellung des wahren Camphenchlorhydrats | |
| DE2120709B2 (de) | Verfahren zur herstellung von, gegebenenfalls durch methyl-, aethyl-, phenyl- und/oder alkoxygruppen mit 1 bis 4 kohlenstoffatomen substituierten, im benzolring eine dimethylaminomethylgruppe enthaltenden chromonen oder cumarinen | |
| AT214437B (de) | Verfahren zur Herstellung von teilhydrierten Anthrazenderivaten | |
| DE513204C (de) | Verfahren zur Darstellung von Kondensationsprodukten aus aromatischen Kohlenwasserstoffen | |
| DE934103C (de) | Verfahren zur Herstellung von cyclooctylierten Alkylessigsaeuren mit stark gallentreibender Wirkung | |
| EP1673363A1 (de) | Verfahren zur herstellung von 1-hydroperoxy-16-oxabicyclo [10.4.0] hexadecan | |
| DE188434C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| DE2560493C2 (de) | 2,9-Dioxatricyclo[4,3,1,0↑3↑↑,↑↑7↑]decane | |
| DE900935C (de) | Verfahren zur Herstellung von 12-Brom-3-acyloxy-5,7,9(11)-pregnatrien-20-on-additionsprodukten | |
| AT227256B (de) | Verfahren zur Herstellung von neuen Aminoindanen und deren Salzen | |
| AT349030B (de) | Verfahren zur herstellung von neuen 8-hydroxy- 3-halogenmethyl-4-acetoxy-10-methylen-2,9- dioxatricyclo(4,3,1,03,7)decanen bzw. der entsprechenden 8-oxo-derivate | |
| DE118351C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| DE736797C (de) | Verfahren zur Herstellung von 5-Acetoxycumaranen oder 6-Acetoxychromanen | |
| AT246931B (de) | Verfahren zur Herstellung von Zwischenverbindungen der Colchicinreihe | |
| DE2415062C3 (de) | Verfahren zur Herstellung von 2-Nitrobenzaldehyd | |
| DE2560594C2 (de) | 2-Oxabicyclo[3,2,1]oct-3-ene | |
| DE921452C (de) | Verfahren zur Herstellung von Furan-ª-carbonsaeuren | |
| DE941062C (de) | Verfahren zur Herstellung von Furan-(2)-carbonsaeurederivaten |