SU461100A1 - Способ получени производных имидазола - Google Patents
Способ получени производных имидазолаInfo
- Publication number
- SU461100A1 SU461100A1 SU1755711A SU1755711A SU461100A1 SU 461100 A1 SU461100 A1 SU 461100A1 SU 1755711 A SU1755711 A SU 1755711A SU 1755711 A SU1755711 A SU 1755711A SU 461100 A1 SU461100 A1 SU 461100A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- general formula
- compound
- imidazole derivatives
- salts
- acylation
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 5
- 150000002460 imidazoles Chemical class 0.000 title claims 2
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 title claims 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 4
- 238000002955 isolation Methods 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims 3
- 230000010933 acylation Effects 0.000 claims 2
- 238000005917 acylation reaction Methods 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 150000001244 carboxylic acid anhydrides Chemical group 0.000 claims 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- -1 1-butyl-4- (acetoxyphenyl) imidazole Chemical compound 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- QREBDEBQNVOXGD-UHFFFAOYSA-N 1-methyl-4-(4-phenylmethoxyphenyl)imidazole Chemical compound CN1C=NC(C=2C=CC(OCC=3C=CC=CC=3)=CC=2)=C1 QREBDEBQNVOXGD-UHFFFAOYSA-N 0.000 description 1
- XEDHZECGVVASLU-UHFFFAOYSA-N 1-methyl-4-(4-phenylmethoxyphenyl)imidazole;hydrochloride Chemical compound Cl.CN1C=NC(C=2C=CC(OCC=3C=CC=CC=3)=CC=2)=C1 XEDHZECGVVASLU-UHFFFAOYSA-N 0.000 description 1
- WYLMHEXTYHPVRI-UHFFFAOYSA-N 4-(1-butylimidazol-4-yl)phenol Chemical compound CCCCN1C=NC(C=2C=CC(O)=CC=2)=C1 WYLMHEXTYHPVRI-UHFFFAOYSA-N 0.000 description 1
- HREKPCHZCTXQJZ-UHFFFAOYSA-N [4-(1-butylimidazol-4-yl)phenyl] acetate;hydrochloride Chemical compound Cl.CCCCN1C=NC(C=2C=CC(OC(C)=O)=CC=2)=C1 HREKPCHZCTXQJZ-UHFFFAOYSA-N 0.000 description 1
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DD15371371 | 1971-03-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU461100A1 true SU461100A1 (ru) | 1975-02-25 |
Family
ID=5483591
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1755711A SU461100A1 (ru) | 1971-03-12 | 1972-03-06 | Способ получени производных имидазола |
Country Status (3)
| Country | Link |
|---|---|
| CH (1) | CH566997A5 (enExample) |
| FR (1) | FR2128292A1 (enExample) |
| SU (1) | SU461100A1 (enExample) |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3558641A (en) * | 1967-10-06 | 1971-01-26 | Merck & Co Inc | Certain pyridyl salicylic acid derivatives |
-
1972
- 1972-01-03 FR FR7200032A patent/FR2128292A1/fr active Granted
- 1972-03-06 SU SU1755711A patent/SU461100A1/ru active
- 1972-03-07 CH CH332272A patent/CH566997A5/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| FR2128292A1 (en) | 1972-10-20 |
| FR2128292B1 (enExample) | 1976-04-16 |
| CH566997A5 (enExample) | 1975-09-30 |
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