CH407133A - Verfahren zur Herstellung eines neuen Oxadiazolinderivates - Google Patents
Verfahren zur Herstellung eines neuen OxadiazolinderivatesInfo
- Publication number
- CH407133A CH407133A CH1503162A CH1503162A CH407133A CH 407133 A CH407133 A CH 407133A CH 1503162 A CH1503162 A CH 1503162A CH 1503162 A CH1503162 A CH 1503162A CH 407133 A CH407133 A CH 407133A
- Authority
- CH
- Switzerland
- Prior art keywords
- salt
- preparation
- new
- aminophenyl
- hydroxy
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 8
- 238000002360 preparation method Methods 0.000 title claims description 6
- JKNSMBZZZFGYCB-UHFFFAOYSA-N 4,5-dihydrooxadiazole Chemical class C1CN=NO1 JKNSMBZZZFGYCB-UHFFFAOYSA-N 0.000 title description 3
- 150000003839 salts Chemical class 0.000 claims description 12
- WUBBRNOQWQTFEX-UHFFFAOYSA-N 4-aminosalicylic acid Chemical compound NC1=CC=C(C(O)=O)C(O)=C1 WUBBRNOQWQTFEX-UHFFFAOYSA-N 0.000 claims description 9
- 229960004909 aminosalicylic acid Drugs 0.000 claims description 9
- 239000000243 solution Substances 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 3
- FVVDKUPCWXUVNP-UHFFFAOYSA-M Aminosalicylate sodium anhydrous Chemical compound [Na+].NC1=CC=C(C([O-])=O)C(O)=C1 FVVDKUPCWXUVNP-UHFFFAOYSA-M 0.000 claims description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 2
- 230000001419 dependent effect Effects 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- FYZGXAKJVDHGDR-UHFFFAOYSA-N aminosalicylic acid hydrazide Chemical compound NNC(=O)C1=CC=C(N)C=C1O FYZGXAKJVDHGDR-UHFFFAOYSA-N 0.000 description 1
- 229950008235 aminosalicylic acid hydrazide Drugs 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- 230000001549 tubercolostatic effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/10—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles
- C07D271/113—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1503162A CH407133A (de) | 1962-12-21 | 1962-12-21 | Verfahren zur Herstellung eines neuen Oxadiazolinderivates |
| AT1019163A AT241458B (de) | 1962-12-21 | 1963-12-18 | Verfahren zur Herstellung eines neuen Oxadiazolinderivates |
| FR967529A FR3262M (fr) | 1962-12-21 | 1964-03-16 | Nouveau médicament présentant notamment des propriétés tuberculostatiques. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1503162A CH407133A (de) | 1962-12-21 | 1962-12-21 | Verfahren zur Herstellung eines neuen Oxadiazolinderivates |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH407133A true CH407133A (de) | 1966-02-15 |
Family
ID=4405727
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH1503162A CH407133A (de) | 1962-12-21 | 1962-12-21 | Verfahren zur Herstellung eines neuen Oxadiazolinderivates |
Country Status (3)
| Country | Link |
|---|---|
| AT (1) | AT241458B (fr) |
| CH (1) | CH407133A (fr) |
| FR (1) | FR3262M (fr) |
-
1962
- 1962-12-21 CH CH1503162A patent/CH407133A/de unknown
-
1963
- 1963-12-18 AT AT1019163A patent/AT241458B/de active
-
1964
- 1964-03-16 FR FR967529A patent/FR3262M/fr active Active
Also Published As
| Publication number | Publication date |
|---|---|
| AT241458B (de) | 1965-07-26 |
| FR3262M (fr) | 1965-04-20 |
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