SU293351A1 - - Google Patents
Info
- Publication number
- SU293351A1 SU293351A1 SU1212809A SU1212809A SU293351A1 SU 293351 A1 SU293351 A1 SU 293351A1 SU 1212809 A SU1212809 A SU 1212809A SU 1212809 A SU1212809 A SU 1212809A SU 293351 A1 SU293351 A1 SU 293351A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- parts
- solution
- methyl
- triazolo
- solid
- Prior art date
Links
- 239000007787 solid Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
- 229940040526 Anhydrous Sodium Acetate Drugs 0.000 description 3
- JIAARYAFYJHUJI-UHFFFAOYSA-L Zinc chloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N acetic acid ethyl ester Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- VMHLLURERBWHNL-UHFFFAOYSA-M sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 239000011592 zinc chloride Substances 0.000 description 3
- 235000005074 zinc chloride Nutrition 0.000 description 3
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- WFPKROAQWOOZSZ-UHFFFAOYSA-N 6-methyl-8-propyl-[1,2,4]triazolo[4,3-a]pyrazin-3-amine Chemical compound CCCC1=NC(C)=CN2C(N)=NN=C12 WFPKROAQWOOZSZ-UHFFFAOYSA-N 0.000 description 2
- 229960000583 Acetic Acid Drugs 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 125000004432 carbon atoms Chemical group C* 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N n-butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- -1 oxy- Chemical class 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 150000003216 pyrazines Chemical class 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N AI2O3 Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 238000005020 pharmaceutical industry Methods 0.000 description 1
- KYQCOXFCLRTKLS-UHFFFAOYSA-N pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000000717 retained Effects 0.000 description 1
- 239000001187 sodium carbonate Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
Related Child Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU853948115A Addition SU1351792A2 (ru) | 1985-06-26 | 1985-06-26 | Устройство дл формовани изделий из бетонных смесей |
| SU874232199A Addition SU1472274A2 (ru) | 1987-04-20 | 1987-04-20 | Устройство дл формовани строительных изделий |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU293351A1 true SU293351A1 (pl) |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4123533A (en) | Fused pyrimidine derivatives and compositions for treating atherosclerosis containing them | |
| SU293351A1 (pl) | ||
| SU508176A3 (ru) | Способ получени аминопроизводных бензофенона | |
| SU368752A1 (pl) | ||
| SU1340585A3 (ru) | Способ получени производных тетразола | |
| RU2042678C1 (ru) | Способ получения 6,7- дихлор -1,5- дигидроимидазо (2,1-(b) -хиназолин-2- (3н)-она, промежуточные для их получения и способ их получения | |
| SU293350A1 (ru) | Способ получения производных пиразина | |
| PL80903B1 (pl) | ||
| JPS6270349A (ja) | 光学的に純粋な４−アミノ−３−ヒドロキシカルボン酸誘導体及びその立体特異的合成方法 | |
| US2524802A (en) | Hydroxybenzenesulfonamidopyridazines and preparation of same | |
| SU453827A3 (ru) | СПОСОБ ПОЛУЧЕНИЯ р-АМИНО-р-ФЕНИЛПРОПИОНОВОЙКИСЛОТЫ | |
| SU845781A3 (ru) | Способ получени производных пирида-зиНОНА или иХ СОлЕй | |
| SU454739A3 (ru) | Способ получени 5(6)-ацилбензимидазолилалкилкарбаматов | |
| US3629253A (en) | Fluorinated 1 2-dihydro-1 2 4-benzotriazines | |
| SU852173A3 (ru) | Способ получени производных дигидРОиМидАзО изОХиНО-лиНА или иХ СОлЕй | |
| US4395547A (en) | Process for preparing 1-substituted-6-n-propyl-8-methylimidazo[1,5-d]-as-triazin-4(3H)-ones | |
| Banks et al. | Hydroxyalkylamides of 4-Arsonophenoxy-and 4-Arsonoanilinoacetic Acids | |
| US3884940A (en) | New bis-(4,7-dihydroxycoumarinyl-3-)-acetic acid | |
| SU115903A1 (ru) | Способ получени соединений р да пиразола, изоксазола и пиримидина | |
| SU1643536A1 (ru) | 5-Амино-3-метилпиразол гидрохлорид как промежуточный продукт в синтезе азо- и трициклических соединений | |
| SU277641A1 (ru) | Способ получения производных пиразина | |
| SU1087518A1 (ru) | Способ получени @ , @ -метилен-бис-( @ -винилсульфонилпропионамида) | |
| SU253686A1 (ru) | Способ получения аминозамещенных фталанов | |
| SU443027A1 (ru) | Способ получени арилгидразида нитромуравьиной кислоты | |
| PL64174B1 (pl) |