SU486508A3 - Способ получени замещенных гуанидинофенилмочевины - Google Patents
Способ получени замещенных гуанидинофенилмочевиныInfo
- Publication number
- SU486508A3 SU486508A3 SU1962679A SU1962679A SU486508A3 SU 486508 A3 SU486508 A3 SU 486508A3 SU 1962679 A SU1962679 A SU 1962679A SU 1962679 A SU1962679 A SU 1962679A SU 486508 A3 SU486508 A3 SU 486508A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- guanidinophenylureas
- producing substituted
- ethanol
- benzene
- solution
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 13
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 7
- -1 beisoate Chemical compound 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 229920006395 saturated elastomer Polymers 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 125000000068 chlorophenyl group Chemical group 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 229940050410 gluconate Drugs 0.000 description 2
- UKWHYYKOEPRTIC-UHFFFAOYSA-N mercury(ii) oxide Chemical compound [Hg]=O UKWHYYKOEPRTIC-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- PHOQVHQSTUBQQK-SQOUGZDYSA-N D-glucono-1,5-lactone Chemical compound OC[C@H]1OC(=O)[C@H](O)[C@@H](O)[C@@H]1O PHOQVHQSTUBQQK-SQOUGZDYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 125000004799 bromophenyl group Chemical group 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 235000012209 glucono delta-lactone Nutrition 0.000 description 1
- 229960003681 gluconolactone Drugs 0.000 description 1
- 239000011874 heated mixture Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 229940101209 mercuric oxide Drugs 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 125000006501 nitrophenyl group Chemical group 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- POXAIQSXNOEQGM-UHFFFAOYSA-N propan-2-ylthiourea Chemical compound CC(C)NC(N)=S POXAIQSXNOEQGM-UHFFFAOYSA-N 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C277/00—Preparation of guanidine or its derivatives, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
- C07C277/04—Preparation of guanidine or its derivatives, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups of guanidine from ammonium thiocyanate
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C279/00—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
- C07C279/18—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of guanidine groups bound to carbon atoms of six-membered aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB77771 | 1971-01-07 | ||
| AT256273A AT319266B (de) | 1971-01-07 | 1972-01-07 | Verfahren zur Herstellung von neuen Guanidinophenylharnstoffderivaten sowie von deren Säureadditionssalzen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU486508A3 true SU486508A3 (ru) | 1975-09-30 |
Family
ID=59268403
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1962679A SU486508A3 (ru) | 1971-01-07 | 1972-01-06 | Способ получени замещенных гуанидинофенилмочевины |
| SU1737801A SU484685A3 (ru) | 1971-01-07 | 1972-01-06 | Способ получени замещенных гуанидинофенилмочевины |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1737801A SU484685A3 (ru) | 1971-01-07 | 1972-01-06 | Способ получени замещенных гуанидинофенилмочевины |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US4024183A (enExample) |
| AR (3) | AR192732A1 (enExample) |
| AT (3) | AT319266B (enExample) |
| AU (1) | AU452832B2 (enExample) |
| BE (1) | BE777781A (enExample) |
| BR (1) | BR7200100D0 (enExample) |
| CA (1) | CA973891A (enExample) |
| CH (3) | CH572465A5 (enExample) |
| CS (3) | CS171246B2 (enExample) |
| DE (1) | DE2200722A1 (enExample) |
| DK (1) | DK133149C (enExample) |
| ES (4) | ES398676A1 (enExample) |
| FR (1) | FR2121621B1 (enExample) |
| GB (1) | GB1311432A (enExample) |
| HU (1) | HU163287B (enExample) |
| IE (1) | IE35903B1 (enExample) |
| IL (1) | IL38451A (enExample) |
| NL (1) | NL7200239A (enExample) |
| NO (1) | NO136358C (enExample) |
| SE (1) | SE374107B (enExample) |
| SU (2) | SU486508A3 (enExample) |
| ZA (1) | ZA718494B (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4327244A1 (de) * | 1993-08-13 | 1995-02-16 | Hoechst Ag | Harnstoffsubstituierte Benzoylguandine, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament |
| EP1148048B1 (en) * | 1997-04-10 | 2005-06-29 | Pharmacia & Upjohn Company LLC | Polyaromatic compounds for treating herpes viral infections |
| ITTO20010110A1 (it) * | 2001-02-08 | 2002-08-08 | Rotta Research Lab | Nuovi derivati benzamidinici dotati di attivita' anti-infiammatoria ed immunosoppressiva. |
| WO2008156573A1 (en) * | 2007-06-12 | 2008-12-24 | Provid Pharmaceuticals, Inc. | Kinase inhibitors, compositions thereof, and methods of use therewith |
| CN107652210B (zh) * | 2017-09-30 | 2021-01-01 | 瑞阳（上海）新药研发有限公司 | 一种胍类化合物或其药学上可接受的盐、其制备方法和应用 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH474486A (de) * | 1965-11-19 | 1969-06-30 | Ciba Geigy | Verfahren zur Herstellung neuer Diphenylharnstoffe |
| US3673241A (en) * | 1968-04-04 | 1972-06-27 | Ciba Geigy Corp | Substituted benzaldehyde guanylhydrazones |
-
1971
- 1971-01-07 GB GB77771A patent/GB1311432A/en not_active Expired
- 1971-12-16 IE IE1594/71A patent/IE35903B1/xx unknown
- 1971-12-20 CA CA130,595A patent/CA973891A/en not_active Expired
- 1971-12-20 ZA ZA718494A patent/ZA718494B/xx unknown
- 1971-12-26 IL IL38451A patent/IL38451A/en unknown
- 1971-12-27 NO NO4851/71A patent/NO136358C/no unknown
- 1971-12-28 SE SE7116738A patent/SE374107B/xx unknown
- 1971-12-30 AR AR239892A patent/AR192732A1/es active
- 1971-12-30 AU AU37454/71A patent/AU452832B2/en not_active Expired
-
1972
- 1972-01-05 DK DK5072*#A patent/DK133149C/da active
- 1972-01-06 CH CH862975A patent/CH572465A5/xx not_active IP Right Cessation
- 1972-01-06 CS CS73*BA patent/CS171246B2/cs unknown
- 1972-01-06 CH CH863075A patent/CH577962A5/xx not_active IP Right Cessation
- 1972-01-06 CH CH19072A patent/CH568280A5/xx not_active IP Right Cessation
- 1972-01-06 BE BE777781A patent/BE777781A/xx unknown
- 1972-01-06 SU SU1962679A patent/SU486508A3/ru active
- 1972-01-06 SU SU1737801A patent/SU484685A3/ru active
- 1972-01-06 CS CS3313*A patent/CS171248B2/cs unknown
- 1972-01-06 CS CS3312*A patent/CS171247B2/cs unknown
- 1972-01-06 FR FR7200312A patent/FR2121621B1/fr not_active Expired
- 1972-01-07 AT AT256273A patent/AT319266B/de not_active IP Right Cessation
- 1972-01-07 ES ES398676A patent/ES398676A1/es not_active Expired
- 1972-01-07 AT AT10572A patent/AT313300B/de not_active IP Right Cessation
- 1972-01-07 BR BR000100/72A patent/BR7200100D0/pt unknown
- 1972-01-07 NL NL7200239A patent/NL7200239A/xx unknown
- 1972-01-07 HU HUIE486A patent/HU163287B/hu unknown
- 1972-01-07 AT AT256373A patent/AT322568B/de not_active IP Right Cessation
- 1972-01-07 DE DE19722200722 patent/DE2200722A1/de active Pending
- 1972-08-11 AR AR243553A patent/AR192969A1/es active
- 1972-08-11 AR AR243554A patent/AR192970A1/es active
-
1974
- 1974-04-30 ES ES0425831A patent/ES425831A1/es not_active Expired
- 1974-04-30 ES ES425830A patent/ES425830A1/es not_active Expired
-
1975
- 1975-10-06 US US05/620,049 patent/US4024183A/en not_active Expired - Lifetime
-
1976
- 1976-01-22 ES ES444526A patent/ES444526A1/es not_active Expired
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SU873873A3 (ru) | Способ получени производных пропанона или их солей | |
| SU674669A3 (ru) | Способ получени производных этанола или их солей | |
| SU486508A3 (ru) | Способ получени замещенных гуанидинофенилмочевины | |
| SU574146A3 (ru) | Способ получени замещенных производных гидразидов -аминооксикарбоновых кислот или их солей | |
| SU686616A3 (ru) | Способ получени производных 3-фтор-6-пиперазинил-морфантридина или их солей | |
| SU502606A3 (ru) | Способ получени бензимидазолов | |
| SU718009A3 (ru) | Способ получени 1-нитро-9-алкиламиноалкиламинакридинов или их солей | |
| IL24007A (en) | Substituted benzimidazoles | |
| US4450292A (en) | Derivatives of phenyl aliphatic carboxylic acids, and use thereof in treating gastric and gastro-duodenal ailments | |
| US3000888A (en) | Process for the production of amino acids | |
| US4450274A (en) | Preparation of ethambutol-diisoniazide methane sulfonic acid salt | |
| IWAMOTO et al. | AMINO ALCOHOLS. XIV. METHOXYL DERIVATIVES OF PHENYLPROPANOLAMINE AND 3, 5-DIHYDROXYPHENYLPROPANOLAMINE (1) | |
| US2827457A (en) | department of commerce | |
| SU501668A3 (ru) | Способ получени производных 2-аминобензиламина | |
| SU509239A3 (ru) | Способ получени -(гетероарил-метил)- 7-дезокси-норморфиновили -норкодеинов | |
| SU482945A3 (ru) | Способ получени 3-(4"бром)или 3,"4"дибром(фенил)-3-(3"-пиридил)-1-(диметиламино)-пропана или его солей | |
| US2691039A (en) | Stilbene-alpha-ketol compounds and process for making the same | |
| SU143810A1 (ru) | Способ получени n-алкоксипроизводных n'-бис-(бета-хлорэтил)-аминометилазобензола | |
| SU455954A1 (ru) | Способ получени 6-метокси-7-оксикумаринов | |
| Cohen et al. | Some Derivatives of 2, 2'-(Phenylimino) diethanol | |
| US2654753A (en) | 2-sulfanilamido-5-aminopyrimidine and salts thereof | |
| US3584044A (en) | 2-substituted tetracyclines | |
| SU449052A1 (ru) | Способ получени 2-р-1,4-диоксо-3замещенных-1,2,3,4-тетрагидроизохинолинов | |
| SU334689A1 (enExample) | ||
| SU436057A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ ИЗОПРОПИЛИДЕНОВЫХ ПРОИЗВОДНЫХ ПИРИДОКСИНАВ ПТ5ФОНЯ mmim |