SU474142A3 - Способ получени производных 2-/5-нитро-2-фурил/-тиено/2,3-пиримидина - Google Patents
Способ получени производных 2-/5-нитро-2-фурил/-тиено/2,3-пиримидинаInfo
- Publication number
- SU474142A3 SU474142A3 SU1955919A SU1955919A SU474142A3 SU 474142 A3 SU474142 A3 SU 474142A3 SU 1955919 A SU1955919 A SU 1955919A SU 1955919 A SU1955919 A SU 1955919A SU 474142 A3 SU474142 A3 SU 474142A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- carbon atoms
- group
- furyl
- thieno
- branched
- Prior art date
Links
- -1 5-nitro-2-furyl Chemical group 0.000 title claims description 17
- 238000004519 manufacturing process Methods 0.000 title 1
- 229940083082 pyrimidine derivative acting on arteriolar smooth muscle Drugs 0.000 title 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 9
- 150000001412 amines Chemical class 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 239000002798 polar solvent Substances 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 3
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical class ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 125000004442 acylamino group Chemical group 0.000 claims 1
- 239000003513 alkali Substances 0.000 claims 1
- 125000006524 alkoxy alkyl amino group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000005122 aminoalkylamino group Chemical group 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000004663 dialkyl amino group Chemical group 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 238000002955 isolation Methods 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 125000005429 oxyalkyl group Chemical group 0.000 claims 1
- 239000010802 sludge Substances 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 235000010288 sodium nitrite Nutrition 0.000 description 5
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 4
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000012433 hydrogen halide Substances 0.000 description 3
- 229910000039 hydrogen halide Inorganic materials 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- NJLBFBWCCUAPAF-UHFFFAOYSA-N 2-(5-bromofuran-2-yl)-4-chlorothieno[2,3-d]pyrimidine Chemical compound N=1C=2SC=CC=2C(Cl)=NC=1C1=CC=C(Br)O1 NJLBFBWCCUAPAF-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 241001481789 Rupicapra Species 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229940040526 anhydrous sodium acetate Drugs 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000031709 bromination Effects 0.000 description 1
- 238000005893 bromination reaction Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- HBLQJCDWGARDSR-UHFFFAOYSA-N n-ethyl-2-(5-nitrofuran-2-yl)thieno[2,3-d]pyrimidin-4-amine Chemical compound N=1C=2SC=CC=2C(NCC)=NC=1C1=CC=C([N+]([O-])=O)O1 HBLQJCDWGARDSR-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000002360 preparation method Methods 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
- 238000010992 reflux Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- DDWBRNXDKNIQDY-UHFFFAOYSA-N thieno[2,3-d]pyrimidine Chemical compound N1=CN=C2SC=CC2=C1 DDWBRNXDKNIQDY-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19712117658 DE2117658A1 (de) | 1971-04-10 | 1971-04-10 | Neue 2-(5-Nitro-2-furyl)-thieno eckige Klammer auf 2,3-d eckige Klammer zu pyrimidine und Verfahren zu ihrer Herstellung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU474142A3 true SU474142A3 (ru) | 1975-06-14 |
Family
ID=5804484
Family Applications (4)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1955919A SU474142A3 (ru) | 1971-04-10 | 1973-07-31 | Способ получени производных 2-/5-нитро-2-фурил/-тиено/2,3-пиримидина |
| SU1953845A SU501673A3 (ru) | 1971-04-10 | 1973-07-31 | Способ получени производных 2-(5-нитро-2-фурил)-тиено(2,3- ) пиримидина |
| SU1953844A SU509234A3 (ru) | 1971-04-10 | 1973-07-31 | Способ получени производных2-(5-нитро-2-фурил)-тиено(2,3- )пиримидина |
| SU1953843A SU500759A3 (ru) | 1971-04-10 | 1973-07-31 | Способ получени производных 2-/5-нитро-2-фурил/-тиено/2,3- д / пиримидина |
Family Applications After (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1953845A SU501673A3 (ru) | 1971-04-10 | 1973-07-31 | Способ получени производных 2-(5-нитро-2-фурил)-тиено(2,3- ) пиримидина |
| SU1953844A SU509234A3 (ru) | 1971-04-10 | 1973-07-31 | Способ получени производных2-(5-нитро-2-фурил)-тиено(2,3- )пиримидина |
| SU1953843A SU500759A3 (ru) | 1971-04-10 | 1973-07-31 | Способ получени производных 2-/5-нитро-2-фурил/-тиено/2,3- д / пиримидина |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US3830813A (enExample) |
| AT (4) | AT318633B (enExample) |
| AU (1) | AU467357B2 (enExample) |
| BE (1) | BE781899A (enExample) |
| BG (4) | BG20605A3 (enExample) |
| CA (1) | CA972370A (enExample) |
| CH (4) | CH583736A5 (enExample) |
| DD (1) | DD98683A5 (enExample) |
| DE (1) | DE2117658A1 (enExample) |
| DK (1) | DK127854B (enExample) |
| ES (2) | ES401589A1 (enExample) |
| FR (1) | FR2132839B1 (enExample) |
| GB (1) | GB1384161A (enExample) |
| HU (1) | HU163362B (enExample) |
| IE (1) | IE36268B1 (enExample) |
| IL (1) | IL39173A (enExample) |
| NL (1) | NL7204782A (enExample) |
| NO (1) | NO129147B (enExample) |
| PH (1) | PH10479A (enExample) |
| PL (1) | PL83559B1 (enExample) |
| RO (5) | RO63034A (enExample) |
| SU (4) | SU474142A3 (enExample) |
| ZA (1) | ZA722415B (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4001412A (en) * | 1972-02-28 | 1977-01-04 | Sumitomo Chemical Company, Limited | 1-Substituted-1,2-dihydrothieno[2,3-d]-pyrimidin-2-one derivatives |
| FI54312C (fi) * | 1972-05-09 | 1978-11-10 | Sumitomo Chemical Co | Foerfarande foer framstaellning av tieno-(2,3-d)pyrimidinderivat med avsoendring av urinsyra i urin utoekande |
| US4054656A (en) * | 1975-09-10 | 1977-10-18 | Mead Johnson & Company | Thieno[2,3-d]pyrimidine antiallergic agents |
| GB1570494A (en) * | 1975-11-28 | 1980-07-02 | Ici Ltd | Thienopyrimidine derivatives and their use as pesticides |
| US6608053B2 (en) * | 2000-04-27 | 2003-08-19 | Yamanouchi Pharmaceutical Co., Ltd. | Fused heteroaryl derivatives |
| EP1425284A2 (en) * | 2001-09-11 | 2004-06-09 | Smithkline Beecham Corporation | Furo- and thienopyrimidine derivatives as angiogenesis inhibitors |
-
1971
- 1971-04-10 DE DE19712117658 patent/DE2117658A1/de active Pending
-
1972
- 1972-04-05 PH PH13419A patent/PH10479A/en unknown
- 1972-04-05 US US00241414A patent/US3830813A/en not_active Expired - Lifetime
- 1972-04-07 AT AT951773A patent/AT318633B/de not_active IP Right Cessation
- 1972-04-07 AT AT951573A patent/AT318632B/de not_active IP Right Cessation
- 1972-04-07 CA CA139,148A patent/CA972370A/en not_active Expired
- 1972-04-07 GB GB1621172A patent/GB1384161A/en not_active Expired
- 1972-04-07 DK DK170772AA patent/DK127854B/da unknown
- 1972-04-07 AT AT301272A patent/AT318618B/de not_active IP Right Cessation
- 1972-04-07 DD DD162149A patent/DD98683A5/xx unknown
- 1972-04-07 AT AT951673A patent/AT319255B/de not_active IP Right Cessation
- 1972-04-07 NO NO01196/72*[A patent/NO129147B/no unknown
- 1972-04-08 RO RO7200077451A patent/RO63034A/ro unknown
- 1972-04-08 RO RO7200077450A patent/RO63015A/ro unknown
- 1972-04-08 PL PL1972154623A patent/PL83559B1/pl unknown
- 1972-04-08 BG BG021464A patent/BG20605A3/xx unknown
- 1972-04-08 RO RO7200077449A patent/RO63033A/ro unknown
- 1972-04-08 BG BG021462A patent/BG20604A3/xx unknown
- 1972-04-08 RO RO7200070471A patent/RO62748A/ro unknown
- 1972-04-08 ES ES401589A patent/ES401589A1/es not_active Expired
- 1972-04-08 RO RO7200077448A patent/RO63014A/ro unknown
- 1972-04-08 BG BG021463A patent/BG19183A3/xx unknown
- 1972-04-08 BG BG20180A patent/BG20810A3/xx unknown
- 1972-04-10 BE BE781899A patent/BE781899A/xx unknown
- 1972-04-10 CH CH870575A patent/CH583736A5/xx not_active IP Right Cessation
- 1972-04-10 FR FR7212539A patent/FR2132839B1/fr not_active Expired
- 1972-04-10 NL NL7204782A patent/NL7204782A/xx unknown
- 1972-04-10 IL IL39173A patent/IL39173A/xx unknown
- 1972-04-10 HU HUTO871A patent/HU163362B/hu unknown
- 1972-04-10 CH CH870375A patent/CH575952A5/xx not_active IP Right Cessation
- 1972-04-10 ZA ZA722415A patent/ZA722415B/xx unknown
- 1972-04-10 IE IE460/72A patent/IE36268B1/xx unknown
- 1972-04-10 CH CH870675A patent/CH567510A5/xx not_active IP Right Cessation
- 1972-04-10 AU AU40957/72A patent/AU467357B2/en not_active Expired
- 1972-04-10 CH CH524972A patent/CH575951A5/xx not_active IP Right Cessation
- 1972-10-11 ES ES407519A patent/ES407519A1/es not_active Expired
-
1973
- 1973-07-31 SU SU1955919A patent/SU474142A3/ru active
- 1973-07-31 SU SU1953845A patent/SU501673A3/ru active
- 1973-07-31 SU SU1953844A patent/SU509234A3/ru active
- 1973-07-31 SU SU1953843A patent/SU500759A3/ru active
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