NO793322L - Nye oksazolderivater og fremgangsmaate for deres fremstilling - Google Patents
Nye oksazolderivater og fremgangsmaate for deres fremstillingInfo
- Publication number
- NO793322L NO793322L NO793322A NO793322A NO793322L NO 793322 L NO793322 L NO 793322L NO 793322 A NO793322 A NO 793322A NO 793322 A NO793322 A NO 793322A NO 793322 L NO793322 L NO 793322L
- Authority
- NO
- Norway
- Prior art keywords
- oxazole
- diphenyl
- amino
- derivatives
- solution
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 6
- 150000007978 oxazole derivatives Chemical class 0.000 claims description 5
- 150000008064 anhydrides Chemical class 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000007858 starting material Substances 0.000 claims description 2
- 125000004149 thio group Chemical group *S* 0.000 claims description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 37
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 31
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 27
- 239000000047 product Substances 0.000 description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 239000000741 silica gel Substances 0.000 description 7
- 229910002027 silica gel Inorganic materials 0.000 description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 5
- 229940093471 ethyl oleate Drugs 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 239000003480 eluent Substances 0.000 description 4
- 238000010828 elution Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- IFABLCIRROMTAN-MDZDMXLPSA-N (e)-1-chlorooctadec-9-ene Chemical compound CCCCCCCC\C=C\CCCCCCCCCl IFABLCIRROMTAN-MDZDMXLPSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 3
- 239000012346 acetyl chloride Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- RZWZRACFZGVKFM-UHFFFAOYSA-N propanoyl chloride Chemical compound CCC(Cl)=O RZWZRACFZGVKFM-UHFFFAOYSA-N 0.000 description 3
- -1 2-ethyl Chemical group 0.000 description 2
- WLAMNBDJUVNPJU-UHFFFAOYSA-N 2-methylbutyric acid Chemical compound CCC(C)C(O)=O WLAMNBDJUVNPJU-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000000921 elemental analysis Methods 0.000 description 2
- 229940093499 ethyl acetate Drugs 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000010898 silica gel chromatography Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 230000003595 spectral effect Effects 0.000 description 2
- 238000010183 spectrum analysis Methods 0.000 description 2
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 2
- LYJAAULCGYJTIU-UHFFFAOYSA-N 2-(2-amino-4,5-diphenyl-3h-1,3-oxazol-2-yl)ethanol Chemical compound O1C(N)(CCO)NC(C=2C=CC=CC=2)=C1C1=CC=CC=C1 LYJAAULCGYJTIU-UHFFFAOYSA-N 0.000 description 1
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 description 1
- ODKHOKLXMBWVOQ-UHFFFAOYSA-N 4,5-diphenyl-1,3-oxazole Chemical class O1C=NC(C=2C=CC=CC=2)=C1C1=CC=CC=C1 ODKHOKLXMBWVOQ-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 235000019439 ethyl acetate Nutrition 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D263/46—Sulfur atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D263/48—Nitrogen atoms not forming part of a nitro radical
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Hematology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Diabetes (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Steroid Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT28825/78A IT1099996B (it) | 1978-10-17 | 1978-10-17 | Derivati del 4,5-difenil-ossazolo 2-ammino o 2-tio sostituiti e procedimento per il loro ottenimento |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO793322L true NO793322L (no) | 1980-04-18 |
Family
ID=11224263
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO793322A NO793322L (no) | 1978-10-17 | 1979-10-15 | Nye oksazolderivater og fremgangsmaate for deres fremstilling |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US4591596A (xx) |
| JP (1) | JPS5589271A (xx) |
| AU (1) | AU533275B2 (xx) |
| BE (1) | BE879440A (xx) |
| CA (1) | CA1122221A (xx) |
| CH (1) | CH645364A5 (xx) |
| CS (1) | CS213305B2 (xx) |
| DD (1) | DD146598A5 (xx) |
| DE (1) | DE2942050C2 (xx) |
| DK (1) | DK151880C (xx) |
| FR (1) | FR2439191A1 (xx) |
| GB (1) | GB2036006B (xx) |
| HU (1) | HU181426B (xx) |
| IL (1) | IL58458A (xx) |
| IT (1) | IT1099996B (xx) |
| LU (1) | LU81788A1 (xx) |
| NL (1) | NL7907661A (xx) |
| NO (1) | NO793322L (xx) |
| SE (1) | SE446533B (xx) |
| SU (1) | SU982540A3 (xx) |
| YU (1) | YU41184B (xx) |
| ZA (1) | ZA795525B (xx) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1099996B (it) * | 1978-10-17 | 1985-09-28 | Anic Spa | Derivati del 4,5-difenil-ossazolo 2-ammino o 2-tio sostituiti e procedimento per il loro ottenimento |
| WO2005039590A1 (en) * | 2003-10-21 | 2005-05-06 | Inspire Pharmaceuticals, Inc. | Non-nucleotide compositions and method for treating pain |
| US20220279810A1 (en) | 2019-08-09 | 2022-09-08 | Zuru (Singapore) Pte. Ltd. | Gummy confectionery-coated non-edible container |
| USD1012421S1 (en) | 2020-08-07 | 2024-01-30 | Zuru (Singapore) Pte. Ltd. | Confectionery |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH506548A (de) * | 1966-08-10 | 1971-04-30 | Serono Ist Farm | Verfahren zur Herstellung von 2-aminsubstituiertem 4,5-Diphenyl-Oxazol |
| FR1538009A (fr) * | 1966-08-10 | 1968-08-30 | Serono Ist Farm | 4, 5-diphényl-oxazols 2-amino-substitués et les procédés de préparation par synthèse propres à les obtenir |
| DE2129012A1 (de) * | 1971-06-11 | 1973-01-04 | Merck Patent Gmbh | Azol-derivate |
| DE2428249C3 (de) * | 1973-07-09 | 1978-12-14 | Serna Ag, Glarus (Schweiz) | Verfahren zur Herstellung von |
| GB1497536A (en) * | 1973-12-17 | 1978-01-12 | Lilly Industries Ltd | 2-acylaminooxazoles methods for their preparation and their use |
| GB1507032A (en) * | 1974-08-06 | 1978-04-12 | Serono Lab | 2-thiol-4,5-diphenyloxazole s-derivatives |
| IT1085524B (it) * | 1977-03-22 | 1985-05-28 | Snam Progetti | Materiali e fibre porose biocompatibili in grado di inglobare sostanze di interesse biologico e metodi per il loro ottenimento |
| IT1099996B (it) * | 1978-10-17 | 1985-09-28 | Anic Spa | Derivati del 4,5-difenil-ossazolo 2-ammino o 2-tio sostituiti e procedimento per il loro ottenimento |
-
1978
- 1978-10-17 IT IT28825/78A patent/IT1099996B/it active
-
1979
- 1979-10-11 AU AU51712/79A patent/AU533275B2/en not_active Ceased
- 1979-10-12 GB GB7935584A patent/GB2036006B/en not_active Expired
- 1979-10-15 LU LU81788A patent/LU81788A1/fr unknown
- 1979-10-15 YU YU2503/79A patent/YU41184B/xx unknown
- 1979-10-15 SE SE7908532A patent/SE446533B/sv not_active IP Right Cessation
- 1979-10-15 NO NO793322A patent/NO793322L/no unknown
- 1979-10-16 ZA ZA00795525A patent/ZA795525B/xx unknown
- 1979-10-16 BE BE0/197669A patent/BE879440A/fr not_active IP Right Cessation
- 1979-10-16 HU HU79EE2699A patent/HU181426B/hu not_active IP Right Cessation
- 1979-10-16 IL IL58458A patent/IL58458A/xx unknown
- 1979-10-16 DD DD79216260A patent/DD146598A5/de not_active IP Right Cessation
- 1979-10-16 CH CH930179A patent/CH645364A5/it not_active IP Right Cessation
- 1979-10-16 FR FR7925705A patent/FR2439191A1/fr active Granted
- 1979-10-16 JP JP13248079A patent/JPS5589271A/ja active Granted
- 1979-10-16 CA CA000337867A patent/CA1122221A/en not_active Expired
- 1979-10-16 DK DK436879A patent/DK151880C/da active
- 1979-10-16 SU SU792834908A patent/SU982540A3/ru active
- 1979-10-17 CS CS797044A patent/CS213305B2/cs unknown
- 1979-10-17 DE DE2942050A patent/DE2942050C2/de not_active Expired
- 1979-10-17 NL NL7907661A patent/NL7907661A/nl not_active Application Discontinuation
-
1983
- 1983-11-17 US US06/552,987 patent/US4591596A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| YU41184B (en) | 1986-12-31 |
| AU533275B2 (en) | 1983-11-17 |
| ZA795525B (en) | 1980-10-29 |
| IL58458A (en) | 1983-06-15 |
| CH645364A5 (it) | 1984-09-28 |
| DK436879A (da) | 1980-04-18 |
| HU181426B (en) | 1983-07-28 |
| JPH0231072B2 (xx) | 1990-07-11 |
| FR2439191B1 (xx) | 1982-06-18 |
| DE2942050C2 (de) | 1986-12-04 |
| DK151880C (da) | 1988-06-06 |
| IT7828825A0 (it) | 1978-10-17 |
| CS213305B2 (en) | 1982-04-09 |
| IT1099996B (it) | 1985-09-28 |
| FR2439191A1 (fr) | 1980-05-16 |
| YU250379A (en) | 1983-04-30 |
| JPS5589271A (en) | 1980-07-05 |
| AU5171279A (en) | 1980-04-24 |
| CA1122221A (en) | 1982-04-20 |
| BE879440A (fr) | 1980-04-16 |
| NL7907661A (nl) | 1980-04-21 |
| GB2036006B (en) | 1983-01-06 |
| SE7908532L (sv) | 1980-04-18 |
| DK151880B (da) | 1988-01-11 |
| SU982540A3 (ru) | 1982-12-15 |
| DD146598A5 (de) | 1981-02-18 |
| DE2942050A1 (de) | 1980-04-24 |
| LU81788A1 (fr) | 1980-01-24 |
| IL58458A0 (en) | 1980-01-31 |
| GB2036006A (en) | 1980-06-25 |
| US4591596A (en) | 1986-05-27 |
| SE446533B (sv) | 1986-09-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SU613724A3 (ru) | Способ получени 8-тиометил-эрголинов или их солей | |
| SU652896A3 (ru) | Способ производства лейрокристина | |
| SE454273B (sv) | Cykliska hydroxiimider till anvendning vid framstellning av cykliska aminosyror samt forfaranden for deras framstellning | |
| CA1058169A (en) | Process for the preparation of adenine derivatives made functional and products obtained therefrom | |
| NO793322L (no) | Nye oksazolderivater og fremgangsmaate for deres fremstilling | |
| US3740411A (en) | Water-soluble antibacterial compounds | |
| JPH01249777A (ja) | 新規なカンプトテシン誘導体及びその製造法 | |
| SU423292A3 (ru) | Способ получения пептидсодержащих эргоалкалоидов | |
| IE47109B1 (en) | Process for preparing auranofin | |
| US4254259A (en) | 2-Amino-5-ethylovalyl-6H-1,3,4-thiadiazine oxime | |
| KR900000266B1 (ko) | 아포빈캐미닉산(apovincaminic-acid)의 에틸에스테르의 제조방법 | |
| US2431967A (en) | Alkyl esters of alpha-acylamino, beta-carboalkoxymethyl mercapto suberic acid | |
| SU455545A3 (ru) | Способ получени пироно-рифамицинов | |
| SU398542A1 (ru) | Способ получения производных 3,3'-дитиенилдисульфида | |
| US3255180A (en) | N-acetyl-7-dehydro-1-deoxy-3, 4-o-isopropylidenelincosamine | |
| SU432719A3 (ru) | Способ получения производных 8-триазол- | |
| Ganapathi et al. | Chemistry of the thiazoles: Part II. Synthesis of 4-aminothiazole derivatives | |
| US2810723A (en) | lysergic acid derivatives acylated at | |
| US4289894A (en) | Pentachlorophenyl-phenyl malonate compound suitable for use as acylating agents | |
| KR800001451B1 (ko) | 1, 3, 5-트리치환 벤젠 유도체의 제법 | |
| Kinoshita et al. | An Acyl Migration with Oxalic Acid | |
| SU253801A1 (ru) | Способ получения метилтио- или метилдитиофосфонатов | |
| US3190895A (en) | Substituted androstan-16alpha-ylacetic acids | |
| SU632693A1 (ru) | Способ получени 3,3"-дизамещенных , "-диметил-2,2"-дииндолилдисульфидов | |
| JPH0219356A (ja) | アミノアセトニトリル誘導体及びその製造方法 |