PL92546B1 - Method of producing new 2,4,5-substituted derivatives of imidazole[cs181711b2] - Google Patents
Method of producing new 2,4,5-substituted derivatives of imidazole[cs181711b2] Download PDFInfo
- Publication number
- PL92546B1 PL92546B1 PL17651272A PL17651272A PL92546B1 PL 92546 B1 PL92546 B1 PL 92546B1 PL 17651272 A PL17651272 A PL 17651272A PL 17651272 A PL17651272 A PL 17651272A PL 92546 B1 PL92546 B1 PL 92546B1
- Authority
- PL
- Poland
- Prior art keywords
- radical
- pyridyl
- formula
- oxazole
- phenyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 19
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 title claims description 14
- 150000002460 imidazoles Chemical class 0.000 title description 3
- -1 alkyl radical Chemical class 0.000 claims description 24
- 239000002253 acid Substances 0.000 claims description 18
- 150000001875 compounds Chemical class 0.000 claims description 18
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 17
- 150000003839 salts Chemical class 0.000 claims description 13
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims description 12
- 150000003254 radicals Chemical class 0.000 claims description 12
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 10
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 9
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 8
- 229910021529 ammonia Inorganic materials 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 239000000460 chlorine Substances 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- HNUALPPJLMYHDK-UHFFFAOYSA-N C[CH]C Chemical group C[CH]C HNUALPPJLMYHDK-UHFFFAOYSA-N 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 239000007858 starting material Substances 0.000 claims 4
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- IIVWHGMLFGNMOW-UHFFFAOYSA-N 2-methylpropane Chemical group C[C](C)C IIVWHGMLFGNMOW-UHFFFAOYSA-N 0.000 claims 1
- 125000004861 4-isopropyl phenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
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- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 claims 1
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical group C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 claims 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 17
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- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 3
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- 235000011152 sodium sulphate Nutrition 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
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- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000008183 oral pharmaceutical preparation Substances 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- NCAIGTHBQTXTLR-UHFFFAOYSA-N phentermine hydrochloride Chemical compound [Cl-].CC(C)([NH3+])CC1=CC=CC=C1 NCAIGTHBQTXTLR-UHFFFAOYSA-N 0.000 description 1
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 239000012451 post-reaction mixture Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000000552 rheumatic effect Effects 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 230000003248 secreting effect Effects 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 239000003930 superacid Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 210000000515 tooth Anatomy 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 230000008673 vomiting Effects 0.000 description 1
- 235000012431 wafers Nutrition 0.000 description 1
Landscapes
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH696771A CH561202A5 (OSRAM) | 1971-05-10 | 1971-05-11 | |
| CH425072A CH579072A5 (OSRAM) | 1971-05-10 | 1972-03-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL92546B1 true PL92546B1 (en) | 1977-04-30 |
Family
ID=25695022
Family Applications (4)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL17651272A PL92546B1 (en) | 1971-05-11 | 1972-05-09 | Method of producing new 2,4,5-substituted derivatives of imidazole[cs181711b2] |
| PL15526372A PL84726B1 (en) | 1971-05-11 | 1972-05-09 | Method of producing new 2,4,5-substituted derivatives of imidazole[cs181711b2] |
| PL17651072A PL92549B1 (en) | 1971-05-11 | 1972-05-09 | Method of producing new 2,4,5-substituted derivatives of imidazole[cs181711b2] |
| PL17650972A PL92552B1 (en) | 1971-05-11 | 1972-05-09 | Method of producing new 2,4,5-substituted derivatives of imidazole[cs181711b2] |
Family Applications After (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL15526372A PL84726B1 (en) | 1971-05-11 | 1972-05-09 | Method of producing new 2,4,5-substituted derivatives of imidazole[cs181711b2] |
| PL17651072A PL92549B1 (en) | 1971-05-11 | 1972-05-09 | Method of producing new 2,4,5-substituted derivatives of imidazole[cs181711b2] |
| PL17650972A PL92552B1 (en) | 1971-05-11 | 1972-05-09 | Method of producing new 2,4,5-substituted derivatives of imidazole[cs181711b2] |
Country Status (17)
| Country | Link |
|---|---|
| JP (1) | JPS5630352B1 (OSRAM) |
| AR (4) | AR194594A1 (OSRAM) |
| CS (4) | CS181711B2 (OSRAM) |
| CY (1) | CY936A (OSRAM) |
| DD (1) | DD97654A5 (OSRAM) |
| ES (1) | ES402563A1 (OSRAM) |
| FI (1) | FI57407C (OSRAM) |
| HK (1) | HK61477A (OSRAM) |
| HU (1) | HU164884B (OSRAM) |
| IE (1) | IE36319B1 (OSRAM) |
| IL (1) | IL39285A (OSRAM) |
| KE (1) | KE2796A (OSRAM) |
| MY (1) | MY7800118A (OSRAM) |
| NO (1) | NO137445C (OSRAM) |
| PL (4) | PL92546B1 (OSRAM) |
| SU (4) | SU456409A3 (OSRAM) |
| YU (6) | YU35878B (OSRAM) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HUE028840T2 (en) * | 2009-02-04 | 2017-01-30 | Otsuka Pharma Factory Inc | Phenylimidazole compounds |
-
1972
- 1972-04-18 FI FI108772A patent/FI57407C/fi active
- 1972-04-24 IL IL39285A patent/IL39285A/xx unknown
- 1972-04-24 IE IE53772A patent/IE36319B1/xx unknown
- 1972-04-28 CY CY93672A patent/CY936A/xx unknown
- 1972-05-09 PL PL17651272A patent/PL92546B1/pl unknown
- 1972-05-09 PL PL15526372A patent/PL84726B1/pl unknown
- 1972-05-09 PL PL17651072A patent/PL92549B1/pl unknown
- 1972-05-09 ES ES402563A patent/ES402563A1/es not_active Expired
- 1972-05-09 PL PL17650972A patent/PL92552B1/pl unknown
- 1972-05-10 NO NO166072A patent/NO137445C/no unknown
- 1972-05-10 SU SU1783894A patent/SU456409A3/ru active
- 1972-05-10 JP JP4555472A patent/JPS5630352B1/ja active Pending
- 1972-05-10 HU HUCI001235 patent/HU164884B/hu unknown
- 1972-05-10 YU YU123372A patent/YU35878B/xx unknown
- 1972-05-10 DD DD16286072A patent/DD97654A5/xx unknown
- 1972-05-11 CS CS316372A patent/CS181711B2/cs unknown
- 1972-05-11 CS CS596176A patent/CS181746B2/cs unknown
- 1972-05-11 CS CS596076A patent/CS181745B2/cs unknown
- 1972-05-11 CS CS596276A patent/CS181747B2/cs unknown
- 1972-05-11 AR AR24195372A patent/AR194594A1/es active
-
1973
- 1973-03-20 AR AR24713273A patent/AR198820A1/es active
- 1973-03-20 AR AR24713473A patent/AR195910A1/es active
- 1973-03-20 AR AR24713373A patent/AR198658A1/es active
- 1973-11-27 SU SU1971712A patent/SU489329A3/ru active
- 1973-11-27 SU SU1971713A patent/SU489330A3/ru active
- 1973-11-27 SU SU1971711A patent/SU502605A3/ru active
-
1977
- 1977-11-15 KE KE279677A patent/KE2796A/xx unknown
- 1977-12-08 HK HK61477A patent/HK61477A/xx unknown
-
1978
- 1978-11-14 YU YU264478A patent/YU35879B/xx unknown
- 1978-11-14 YU YU264578A patent/YU35880B/xx unknown
- 1978-11-14 YU YU264678A patent/YU35881B/xx unknown
- 1978-12-30 MY MY7800118A patent/MY7800118A/xx unknown
-
1979
- 1979-04-09 YU YU83779A patent/YU35883B/xx unknown
-
1980
- 1980-01-23 YU YU17680A patent/YU36165B/xx unknown
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