SU489315A3 - Способ получени производных фенилгуанидина - Google Patents
Способ получени производных фенилгуанидинаInfo
- Publication number
- SU489315A3 SU489315A3 SU1963844A SU1963844A SU489315A3 SU 489315 A3 SU489315 A3 SU 489315A3 SU 1963844 A SU1963844 A SU 1963844A SU 1963844 A SU1963844 A SU 1963844A SU 489315 A3 SU489315 A3 SU 489315A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- phenylguanidine
- obtaining derivatives
- coax
- butyl
- compounds
- Prior art date
Links
- 238000000034 method Methods 0.000 title description 6
- QRJZGVVKGFIGLI-UHFFFAOYSA-N 2-phenylguanidine Chemical class NC(=N)NC1=CC=CC=C1 QRJZGVVKGFIGLI-UHFFFAOYSA-N 0.000 title 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
- 125000000066 S-methyl group Chemical group [H]C([H])([H])S* 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C281/00—Derivatives of carbonic acid containing functional groups covered by groups C07C269/00 - C07C279/00 in which at least one nitrogen atom of these functional groups is further bound to another nitrogen atom not being part of a nitro or nitroso group
- C07C281/16—Compounds containing any of the groups, e.g. aminoguanidine
-
- 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
-
- 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
- C07C279/20—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylguanidines
- C07C279/24—Y being a hetero atom
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)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Furan Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2250911A DE2250911A1 (de) | 1972-10-18 | 1972-10-18 | Phenylguanidin-derivate, ein verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel |
Publications (1)
Publication Number | Publication Date |
---|---|
SU489315A3 true SU489315A3 (ru) | 1975-10-25 |
Family
ID=5859304
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU1963844A SU489315A3 (ru) | 1972-10-18 | 1973-10-12 | Способ получени производных фенилгуанидина |
Country Status (23)
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2651467A1 (de) * | 1976-11-11 | 1978-05-18 | Bayer Ag | Substituierte o-phenylendiaminderivate, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel |
US6593466B1 (en) | 1999-07-07 | 2003-07-15 | Isis Pharmaceuticals, Inc. | Guanidinium functionalized nucleotides and precursors thereof |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2108835A1 (en) * | 1970-10-09 | 1972-05-26 | Rhone Poulenc Sa | Fungicidal guanidines from o phenylenediamine |
DE2109454A1 (en) * | 1971-02-27 | 1972-09-14 | Farbenfabriken Bayer Ag, 5090 Leverkusen | Fungicidal n-(2-acylaminophenyl)-n,n-bis(alkoxycarbonyl)-guanidines - from 2-acrylaminoanilines and s-alkyl n,n-bis(alkoxycarbonyl) isothiazole |
-
1972
- 1972-10-18 DE DE2250911A patent/DE2250911A1/de active Pending
-
1973
- 1973-10-12 SU SU1963844A patent/SU489315A3/ru active
- 1973-10-15 NL NL7314183A patent/NL7314183A/xx not_active Application Discontinuation
- 1973-10-16 IL IL43431A patent/IL43431A/en unknown
- 1973-10-16 AT AT878973A patent/AT338818B/de not_active IP Right Cessation
- 1973-10-16 LU LU68627A patent/LU68627A1/xx unknown
- 1973-10-16 EG EG403A patent/EG11195A/xx active
- 1973-10-16 JP JP48115397A patent/JPS4971123A/ja active Pending
- 1973-10-16 AR AR250542A patent/AR199121A1/es active
- 1973-10-16 CS CS7129A patent/CS168049B2/cs unknown
- 1973-10-16 CH CH1465073A patent/CH586195A5/xx not_active IP Right Cessation
- 1973-10-16 JP JP48115396A patent/JPS4986341A/ja active Pending
- 1973-10-17 ZA ZA738075*A patent/ZA738075B/xx unknown
- 1973-10-17 CA CA183,615A patent/CA992554A/en not_active Expired
- 1973-10-17 PH PH15116A patent/PH10760A/en unknown
- 1973-10-17 BE BE136796A patent/BE806201A/xx unknown
- 1973-10-17 ES ES419721A patent/ES419721A1/es not_active Expired
- 1973-10-17 GB GB4838673A patent/GB1414244A/en not_active Expired
- 1973-10-17 IE IE1854/73A patent/IE38387B1/xx unknown
- 1973-10-17 AU AU61505/73A patent/AU475701B2/en not_active Expired
- 1973-10-17 SE SE7314109A patent/SE386436B/xx unknown
- 1973-10-18 FR FR7337211A patent/FR2203631B1/fr not_active Expired
- 1973-10-18 HU HUBA2987A patent/HU166358B/hu unknown
-
1976
- 1976-05-18 KE KE2628*UA patent/KE2628A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
FR2203631B1 (enrdf_load_stackoverflow) | 1977-09-09 |
EG11195A (en) | 1977-11-30 |
NL7314183A (enrdf_load_stackoverflow) | 1974-04-22 |
ES419721A1 (es) | 1976-03-01 |
IE38387L (en) | 1974-04-18 |
SE386436B (sv) | 1976-08-09 |
LU68627A1 (enrdf_load_stackoverflow) | 1973-12-27 |
KE2628A (en) | 1976-05-28 |
IL43431A (en) | 1976-04-30 |
ZA738075B (en) | 1974-08-28 |
GB1414244A (en) | 1975-11-19 |
CA992554A (en) | 1976-07-06 |
JPS4971123A (enrdf_load_stackoverflow) | 1974-07-10 |
AT338818B (de) | 1977-09-12 |
CH586195A5 (enrdf_load_stackoverflow) | 1977-03-31 |
AR199121A1 (es) | 1974-08-08 |
BE806201A (fr) | 1974-04-17 |
IE38387B1 (en) | 1978-03-01 |
DE2250911A1 (de) | 1974-04-25 |
AU6150573A (en) | 1975-04-17 |
JPS4986341A (enrdf_load_stackoverflow) | 1974-08-19 |
CS168049B2 (enrdf_load_stackoverflow) | 1976-05-28 |
HU166358B (enrdf_load_stackoverflow) | 1975-03-28 |
IL43431A0 (en) | 1974-01-14 |
AU475701B2 (en) | 1976-09-02 |
ATA878973A (de) | 1977-01-15 |
FR2203631A1 (enrdf_load_stackoverflow) | 1974-05-17 |
PH10760A (en) | 1977-09-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
SU489315A3 (ru) | Способ получени производных фенилгуанидина | |
SU498903A3 (ru) | Способ получени замещенных бензоилфенилгуанидина | |
DE1745624C3 (de) | Verfahren zur Herstellung von Derivaten des Cephalosporin C | |
US2959614A (en) | 2-amino-3 (beta-aminoethyoxy)-propionic acid and its dihydrochloride salt | |
SU607549A3 (ru) | Способ получени производных карбалкокситиоуреидобензола | |
SU334806A1 (ru) | Способ получени 3-оксиметилроданинов | |
Tauber | Phenylalanylphenylalanine ethyl ester synthesis by chymotrypsin | |
SU558639A3 (ru) | Способ получени производных аминооксигидроксамовой кислоты или их солей | |
SU539529A3 (ru) | Способ получени амидов бензимидазол1-карбоновой кислоты | |
GB1501527A (en) | Process for the preparation of 3-(3,5-dichlorophenyl)-hydantoin | |
SU591140A3 (ru) | Способ получени 2-(3"-метокси4"-гидроксифенил)-индола | |
SU422735A1 (ru) | Способ получения амидов 2-окси-1,6-дигидро-5- пиримидинкарбоновой кислоты | |
SU92204A1 (ru) | Способ сенсибилизации галоидосеребр ных фотоэмульсий | |
SU502896A1 (ru) | Способ получени бис(приорганилсилил) сульфатов | |
SU436055A1 (ru) | Способ получения 1-фенил-4,5- дихлорпиридазона-6 | |
Frankel et al. | 82. Syntheses of some polymeric polypeptides of lanthionine | |
SU458557A1 (ru) | Способ получени 2-(ацетилметил)бензо-1,3-оксатиолов | |
SU513028A1 (ru) | Этиловый эфир п-толилсульфонилпировиноградной кислоты,про вл ющий анальгетическую активность | |
SU493470A1 (ru) | Способ получени производных 12-аминоиндоло -(1,2 с) хиназолина или их солей | |
SU436057A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ ИЗОПРОПИЛИДЕНОВЫХ ПРОИЗВОДНЫХ ПИРИДОКСИНАВ ПТ5ФОНЯ mmim | |
SU106839A1 (ru) | Способ получени альфа, бета-непредельных эфиров арилсульфокислот | |
SU529171A1 (ru) | Способ получени производных 1,8-оксазадекалонов-4 | |
SU771101A1 (ru) | 1- / - / -Метакрилоил- -аминолауроил/оксиэтил -3,3-диметил-6-нитроспиро/2н-1бензопиран-2,2-индолин, как полупродукт дл фотохромных материалов | |
SU422148A3 (ru) | Способ получения производных инденопиридина | |
SU481600A1 (ru) | Способ получени аминоэпоксикетонов |