DE297243C - - Google Patents
Info
- Publication number
- DE297243C DE297243C DENDAT297243D DE297243DA DE297243C DE 297243 C DE297243 C DE 297243C DE NDAT297243 D DENDAT297243 D DE NDAT297243D DE 297243D A DE297243D A DE 297243DA DE 297243 C DE297243 C DE 297243C
- Authority
- DE
- Germany
- Prior art keywords
- aminophenyl ester
- salicylic acid
- bromo
- acid
- aminophenyl
- 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
- CSWNCAHMIZQPOZ-UHFFFAOYSA-N (4-aminophenyl) 2-hydroxybenzoate Chemical class C1=CC(N)=CC=C1OC(=O)C1=CC=CC=C1O CSWNCAHMIZQPOZ-UHFFFAOYSA-N 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- -1 α-bromoisovalerianyl Chemical group 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- DNVVZWSVACQWJE-UHFFFAOYSA-N 4-amino-2-hydroxybenzoic acid phenyl ester Chemical compound OC1=CC(N)=CC=C1C(=O)OC1=CC=CC=C1 DNVVZWSVACQWJE-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 230000003356 anti-rheumatic effect Effects 0.000 description 1
- 239000003435 antirheumatic agent Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000000932 sedative agent Substances 0.000 description 1
- 230000001624 sedative effect Effects 0.000 description 1
- 230000007958 sleep Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 230000009967 tasteless effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/16—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE297243C true DE297243C (enrdf_load_stackoverflow) |
Family
ID=551555
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT297243D Active DE297243C (enrdf_load_stackoverflow) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE297243C (enrdf_load_stackoverflow) |
-
0
- DE DENDAT297243D patent/DE297243C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1620024C3 (de) | 3'-Pyridylmethyl-2-(4-chlorphenoxy)-2-methylpropionat | |
| DE1518019A1 (de) | 2-(4-Chlorphenoxy)-2-methylpropionaldehyd und Verfahren zu dessen Herstellung | |
| DE69502572T2 (de) | Verfahren zur Herstellung von Geranylgeraniol | |
| DE297243C (enrdf_load_stackoverflow) | ||
| AT139454B (de) | Verfahren zur Darstellung von Alkaminestern. | |
| DE708513C (de) | Verfahren zur Herstellung von Oxymethylencarbonsaeureestern durch Kondensation von Ameisensaeureestern mit aliphatischen Carbonsaeureestern | |
| DE2617746A1 (de) | Oberflaechenaktives mittel mit hoher ausbreitgeschwindigkeit auf kohlenwasserstoffen | |
| DE544087C (de) | Verfahren zur Darstellung aromatischer N-Dialkylaminoalkylaminoaldehyde und ihrer Derivate | |
| DE276809C (enrdf_load_stackoverflow) | ||
| DE724757C (de) | Verfahren zur Herstellung von Diazoketonen | |
| DE879840C (de) | Verfahren zur Herstellung von Estern von Aminopropandiolen | |
| EP0061641B1 (de) | Verfahren zur Herstellung von Caronaldehydsäure und deren Derivaten | |
| DE2044251C3 (de) | und | |
| DE511093C (de) | Verfahren zur Darstellung eines Salicylsaeuredihalogenalkylesters | |
| DE230172C (enrdf_load_stackoverflow) | ||
| DE442414C (de) | Verfahren zur Darstellung einer Amino-3-chlor-4-oxybenzol-1-arsinsaeure | |
| DE715267C (de) | Verfahren zur Herstellung von neutralen, oelloeslichen und sterilisierbaren organischen Wismutsalzen | |
| DE291878C (enrdf_load_stackoverflow) | ||
| DE1802656B2 (de) | 3,3-Diphenylpropylaminoalkanolester, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Arzneimittel | |
| DE638418C (de) | Verfahren zur Gewinnung von Abkoemmlingen der Nucleotide | |
| DE80216C (enrdf_load_stackoverflow) | ||
| DE729851C (de) | Verfahren zur Herstellung von 5, 5-Diphenyl-2, 4-dioxooxazolidin | |
| AT218509B (de) | Verfahren zur Herstellung von basisch substituierten Carbinolen, sowie von ihren sterisch einheitlichen Razematen und deren optisch aktiven Komponenten und/oder ihren Säureadditionssalzen | |
| DE1814649A1 (de) | Verfahren zur Herstellung von 1,2-Diphenyl-3,5-dioxopyrazolidin und dessen Substitutionsprodukten | |
| DE1003744B (de) | Verfahren zur Herstellung parasympathicolytisch aktiver ª‡, ª‡-Diphenyl-ª†-dialkylaminobutyramide |