SU436494A3 - Способ получения n,n'-ди[пиpиmидил- - Google Patents
Способ получения n,n'-ди[пиpиmидил-Info
- Publication number
- SU436494A3 SU436494A3 SU1106159A SU1106159A SU436494A3 SU 436494 A3 SU436494 A3 SU 436494A3 SU 1106159 A SU1106159 A SU 1106159A SU 1106159 A SU1106159 A SU 1106159A SU 436494 A3 SU436494 A3 SU 436494A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- methyl
- amino
- alk
- mixture
- hours
- Prior art date
Links
- 238000000034 method Methods 0.000 title description 12
- 229910052757 nitrogen Inorganic materials 0.000 title description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 12
- 239000000203 mixture Substances 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 125000005843 halogen group Chemical group 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 6
- 235000019270 ammonium chloride Nutrition 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000000155 melt Substances 0.000 description 6
- 235000011121 sodium hydroxide Nutrition 0.000 description 6
- 125000003277 amino group Chemical group 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 5
- 239000002244 precipitate Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- MEFOLQWSRBDONE-UHFFFAOYSA-N 6-chloro-n,n,2-trimethylpyrimidin-4-amine Chemical compound CN(C)C1=CC(Cl)=NC(C)=N1 MEFOLQWSRBDONE-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- QLEIDMAURCRVCX-UHFFFAOYSA-N 1-propylpiperazine Chemical compound CCCN1CCNCC1 QLEIDMAURCRVCX-UHFFFAOYSA-N 0.000 description 2
- LWQNWCVIJDSVNQ-UHFFFAOYSA-N 2,5-dimethyl-1-propylpiperazine Chemical compound CCCN1CC(C)NCC1C LWQNWCVIJDSVNQ-UHFFFAOYSA-N 0.000 description 2
- -1 2-methyl-6-dimethylamino-4-methylmercaptopyrimidine Chemical compound 0.000 description 2
- GSXFOGXQLRLSKK-UHFFFAOYSA-N 4-chloro-2,6-dimethylpyrimidine Chemical compound CC1=CC(Cl)=NC(C)=N1 GSXFOGXQLRLSKK-UHFFFAOYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000003302 alkenyloxy group Chemical group 0.000 description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 2
- GVBHCMNXRKOJRH-UHFFFAOYSA-N 2,4,5,6-tetrachloropyrimidine Chemical compound ClC1=NC(Cl)=C(Cl)C(Cl)=N1 GVBHCMNXRKOJRH-UHFFFAOYSA-N 0.000 description 1
- UVLSCMIEPPWCHZ-UHFFFAOYSA-N 3-piperazin-1-ylpropan-1-amine Chemical compound NCCCN1CCNCC1 UVLSCMIEPPWCHZ-UHFFFAOYSA-N 0.000 description 1
- KGFUGLZSONHTTJ-UHFFFAOYSA-N 3-piperazin-1-ylpropane-1,1-diamine Chemical compound NC(N)CCN1CCNCC1 KGFUGLZSONHTTJ-UHFFFAOYSA-N 0.000 description 1
- JDYDIHVYOFAERC-UHFFFAOYSA-N 4-chloro-n,n,6-trimethylpyrimidin-2-amine Chemical compound CN(C)C1=NC(C)=CC(Cl)=N1 JDYDIHVYOFAERC-UHFFFAOYSA-N 0.000 description 1
- SSAYHQQUDKQNAC-UHFFFAOYSA-N 6-chloro-2-methylpyrimidin-4-amine Chemical compound CC1=NC(N)=CC(Cl)=N1 SSAYHQQUDKQNAC-UHFFFAOYSA-N 0.000 description 1
- TVPZEVZEMNVSAS-UHFFFAOYSA-N 6-chloro-n,2-dimethylpyrimidin-4-amine Chemical compound CNC1=CC(Cl)=NC(C)=N1 TVPZEVZEMNVSAS-UHFFFAOYSA-N 0.000 description 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- WEYVCQFUGFRXOM-UHFFFAOYSA-N perazine Chemical compound C1CN(C)CCN1CCCN1C2=CC=CC=C2SC2=CC=CC=C21 WEYVCQFUGFRXOM-UHFFFAOYSA-N 0.000 description 1
- 229960002195 perazine Drugs 0.000 description 1
- 125000001500 prolyl group Chemical group [H]N1C([H])(C(=O)[*])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/50—Three nitrogen atoms
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1751468A CH499528A (de) | 1965-10-22 | 1965-10-22 | Verfahren zur Herstellung neuer Pyrimidine |
| CH506468A CH478818A (de) | 1965-10-22 | 1965-10-22 | Verfahren zur Herstellung neuer N,N'-Di-(pyrimidyl-(4)-aminoalkyl)-diazacycloalkanen |
| CH1463065A CH478816A (de) | 1965-10-22 | 1965-10-22 | Verfahren zur Herstellung neuer N,N'-Di-(pyrimidyl-(4)-aminoalkyl)-diazacycloalkanen |
| CH506368A CH478817A (de) | 1965-10-22 | 1965-10-22 | Verfahren zur Herstellung neuer N,N'-Di-(pyrimidyl-(4)-aminoalkyl)-diazacycloalkanen |
| CH506568A CH478819A (de) | 1965-10-22 | 1965-10-22 | Verfahren zur Herstellung neuer N,N'-Di-(pyrimidyl-(4)-aminoalkyl)-diazacycloalkanen |
| CH1133066 | 1966-08-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU436494A3 true SU436494A3 (ru) | 1974-07-15 |
Family
ID=27543760
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1106159A SU436494A3 (ru) | 1965-10-22 | 1966-10-07 | Способ получения n,n'-ди[пиpиmидил- |
| SU1335465A SU427513A3 (ru) | 1965-10-22 | 1966-10-07 | Способ получения производных пиримидина |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1335465A SU427513A3 (ru) | 1965-10-22 | 1966-10-07 | Способ получения производных пиримидина |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US3503963A (enExample) |
| BE (1) | BE688660A (enExample) |
| BR (1) | BR6683919D0 (enExample) |
| CH (5) | CH478817A (enExample) |
| DE (1) | DE1670392A1 (enExample) |
| FR (3) | FR1500479A (enExample) |
| GB (1) | GB1135259A (enExample) |
| IL (1) | IL26473A (enExample) |
| NL (1) | NL6614961A (enExample) |
| SE (1) | SE345273B (enExample) |
| SU (2) | SU436494A3 (enExample) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH485754A (de) * | 1966-07-28 | 1970-02-15 | Ciba Geigy | Verfahren zur Herstellung neuer Aminopyrimidine |
| HRP20050696B1 (en) | 2003-01-14 | 2008-10-31 | Arena Pharmaceuticals Inc. | 1,2,3-trisubstituted aryl and heteroaryl derivatives as modulators of metabolism and the prpphylaxis and treatment of disorders related thereto such as diabetes and hyperglycemia |
| ES2316964T3 (es) * | 2003-02-24 | 2009-04-16 | Arena Pharmaceuticals, Inc. | Fenil-y piridilpipereidinia-derivados como moduladores del metabolismo de la glucosa. |
| AR045047A1 (es) | 2003-07-11 | 2005-10-12 | Arena Pharm Inc | Derivados arilo y heteroarilo trisustituidos como moduladores del metabolismo y de la profilaxis y tratamiento de desordenes relacionados con los mismos |
| UA92150C2 (ru) * | 2004-06-04 | 2010-10-11 | Арена Фармасьютикалз, Инк. | Замещенные производные арила и гетероарила как модуляторы метаболизма и для профилактики и лечения связанных с ним расстройств |
| HN2005000795A (es) * | 2004-10-15 | 2010-08-19 | Aventis Pharma Inc | Pirimidinas como antagonistas del receptor de prostaglandina d2 |
| MY148521A (en) | 2005-01-10 | 2013-04-30 | Arena Pharm Inc | Substituted pyridinyl and pyrimidinyl derivatives as modulators of metabolism and the treatment of disorders related thereto |
| DOP2006000010A (es) | 2005-01-10 | 2006-07-31 | Arena Pharm Inc | Procedimiento para preparar eteres aromáticos |
| ATE429430T1 (de) * | 2005-09-16 | 2009-05-15 | Arena Pharm Inc | Stoffwechselmodulatoren und behandlung damit verbundener erkrankungen |
| TW200811140A (en) * | 2006-07-06 | 2008-03-01 | Arena Pharm Inc | Modulators of metabolism and the treatment of disorders related thereto |
| TW200811147A (en) * | 2006-07-06 | 2008-03-01 | Arena Pharm Inc | Modulators of metabolism and the treatment of disorders related thereto |
| SG182610A1 (en) | 2010-01-27 | 2012-08-30 | Arena Pharm Inc | Processes for the preparation of (r)-2-(7-(4-cyclopentyl-3-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid and salts thereof |
| MX2013003184A (es) | 2010-09-22 | 2013-06-07 | Arena Pharm Inc | Moduladores del receptor gpr119 y el tratamiento de transtornos relacionados con el mismo. |
| US11007175B2 (en) | 2015-01-06 | 2021-05-18 | Arena Pharmaceuticals, Inc. | Methods of treating conditions related to the S1P1 receptor |
| BR112017027656B1 (pt) | 2015-06-22 | 2023-12-05 | Arena Pharmaceuticals, Inc. | Hábito cristalino de placa livre de sal de l-arginina de ácido (r)-2-(7-(4- ciclopentil-3-(trifluorometil)benzilóxi)- 1,2,3,4-tetra-hidrociclo-penta[b]indol-3- il)acético, composição farmacêutica que o compreende, seus usos e método de preparação do mesmo |
| CA3053418A1 (en) | 2017-02-16 | 2018-08-23 | Arena Pharmaceuticals, Inc. | Compounds and methods for treatment of primary biliary cholangitis |
| BR112020024762A2 (pt) | 2018-06-06 | 2021-03-23 | Arena Pharmaceuticals, Inc. | métodos de tratamento de condições relacionadas ao receptor s1p1 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB944443A (enExample) * | 1959-09-25 | 1900-01-01 |
-
1965
- 1965-10-22 CH CH506368A patent/CH478817A/de not_active IP Right Cessation
- 1965-10-22 CH CH1751468A patent/CH499528A/de not_active IP Right Cessation
- 1965-10-22 CH CH506468A patent/CH478818A/de not_active IP Right Cessation
- 1965-10-22 CH CH1463065A patent/CH478816A/de not_active IP Right Cessation
- 1965-10-22 CH CH506568A patent/CH478819A/de not_active IP Right Cessation
-
1966
- 1966-09-07 IL IL26473A patent/IL26473A/en unknown
- 1966-10-07 SU SU1106159A patent/SU436494A3/ru active
- 1966-10-07 SU SU1335465A patent/SU427513A3/ru active
- 1966-10-14 FR FR80113A patent/FR1500479A/fr not_active Expired
- 1966-10-14 DE DE19661670392 patent/DE1670392A1/de active Pending
- 1966-10-17 GB GB46245/66A patent/GB1135259A/en not_active Expired
- 1966-10-21 BR BR183919/66A patent/BR6683919D0/pt unknown
- 1966-10-21 SE SE14418/66A patent/SE345273B/xx unknown
- 1966-10-21 NL NL6614961A patent/NL6614961A/xx unknown
- 1966-10-21 BE BE688660D patent/BE688660A/xx unknown
- 1966-11-30 US US597870A patent/US3503963A/en not_active Expired - Lifetime
-
1967
- 1967-01-05 FR FR90061A patent/FR6083M/fr not_active Expired
- 1967-01-05 FR FR90062A patent/FR6084M/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| CH478816A (de) | 1969-09-30 |
| US3503963A (en) | 1970-03-31 |
| SU427513A3 (ru) | 1974-05-05 |
| FR1500479A (fr) | 1967-11-03 |
| GB1135259A (en) | 1968-12-04 |
| CH499528A (de) | 1970-11-30 |
| BE688660A (enExample) | 1967-04-21 |
| CH478819A (de) | 1969-09-30 |
| CH478817A (de) | 1969-09-30 |
| IL26473A (en) | 1971-08-25 |
| FR6083M (enExample) | 1968-06-04 |
| BR6683919D0 (pt) | 1973-12-04 |
| SE345273B (enExample) | 1972-05-23 |
| FR6084M (enExample) | 1968-06-04 |
| DE1670392A1 (de) | 1970-07-16 |
| CH478818A (de) | 1969-09-30 |
| NL6614961A (enExample) | 1967-04-24 |
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