SU410013A1 - - Google Patents
Info
- Publication number
- SU410013A1 SU410013A1 SU711696562A SU1696562A SU410013A1 SU 410013 A1 SU410013 A1 SU 410013A1 SU 711696562 A SU711696562 A SU 711696562A SU 1696562 A SU1696562 A SU 1696562A SU 410013 A1 SU410013 A1 SU 410013A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- pyridine
- esters
- acetylene
- nicotinic
- treated
- Prior art date
Links
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 16
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 7
- -1 nicotine esters esters Chemical class 0.000 claims description 5
- 238000002360 preparation method Methods 0.000 claims description 3
- WZIYCIBURCPKAR-UHFFFAOYSA-N 4-(chloromethyl)pyridine Chemical class ClCC1=CC=NC=C1 WZIYCIBURCPKAR-UHFFFAOYSA-N 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 150000003512 tertiary amines Chemical class 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical group N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- PVNIIMVLHYAWGP-UHFFFAOYSA-N nicotinic acid Natural products OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 2
- TWBYWOBDOCUKOW-UHFFFAOYSA-N isonicotinic acid Chemical class OC(=O)C1=CC=NC=C1 TWBYWOBDOCUKOW-UHFFFAOYSA-N 0.000 description 2
- CNQCWYFDIQSALX-UHFFFAOYSA-N 3-(chloromethyl)pyridine Chemical compound ClCC1=CC=CN=C1 CNQCWYFDIQSALX-UHFFFAOYSA-N 0.000 description 1
- OUYZXXMYLVNZAQ-UHFFFAOYSA-N 4-(chloromethyl)pyridine hypochlorous acid Chemical class ClO.N1=CC=C(C=C1)CCl OUYZXXMYLVNZAQ-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 241000289669 Erinaceus europaeus Species 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Natural products CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- ATBIAJXSKNPHEI-UHFFFAOYSA-N pyridine-3-carbonyl chloride Chemical class ClC(=O)C1=CC=CN=C1 ATBIAJXSKNPHEI-UHFFFAOYSA-N 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Pyridine Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU711696562A SU410013A1 (cg-RX-API-DMAC7.html) | 1971-09-01 | 1971-09-01 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU711696562A SU410013A1 (cg-RX-API-DMAC7.html) | 1971-09-01 | 1971-09-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU410013A1 true SU410013A1 (cg-RX-API-DMAC7.html) | 1974-01-05 |
Family
ID=20487708
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU711696562A SU410013A1 (cg-RX-API-DMAC7.html) | 1971-09-01 | 1971-09-01 |
Country Status (1)
| Country | Link |
|---|---|
| SU (1) | SU410013A1 (cg-RX-API-DMAC7.html) |
-
1971
- 1971-09-01 SU SU711696562A patent/SU410013A1/ru active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SU410013A1 (cg-RX-API-DMAC7.html) | ||
| DD229126A5 (de) | Verfahren zur herstellung von tetronsaeure | |
| US2800482A (en) | Olefinic derivatives of 8-alkylnortropanes and the acid and quaternary ammonium salts thereof | |
| DE2607294A1 (de) | Verfahren zur herstellung von 2-amino-1-butanol | |
| SU505359A3 (ru) | Способ получени производных изоиндолина или их солей | |
| JPH11507662A (ja) | 抗虚血性ヒドロキシルアミン誘導体および医薬組成物 | |
| SU585808A3 (ru) | Способ получени -амино-2-адамантилуксусной кислоты | |
| SU486016A1 (ru) | Способ получени никотиноилэтилендиамина или его солей | |
| SU979344A1 (ru) | Способ получени 4-метил-5- @ -оксиэтилтиазола | |
| US2970159A (en) | Hydrazine derivatives | |
| SU899553A1 (ru) | Способ получени 2-метил-3-этоксикарбонил-хиноксалинов | |
| DE2362687A1 (de) | Verfahren zur razematspaltung von d,l-penicillamin | |
| NO137498B (no) | Mellomprodukt for fremstilling av lokalanestetisk virksomt 2-(n-n-propyl-tert.-amylamino)-2`, 6`-acetoxylidid | |
| SU480216A3 (ru) | Способ получени -(аминофенил)алифатических производных карбоновых кислот или их солей,или их -окисей | |
| US2948733A (en) | Intermediates for pyridoxine and process | |
| NO136460B (cg-RX-API-DMAC7.html) | ||
| SU711035A1 (ru) | Способ получени 2-аминопроизводных 5-этилфеназинона-3 | |
| US3024245A (en) | Process for producing pyridoxine and intermediates | |
| SU545263A3 (ru) | Способ получени этилового эфира аповинкаминовой кислоты или его йодметилата | |
| DE2950378C2 (de) | N-eckige Klammer auf 2-(3-Benzoylpheny)-propionyläthylendioxyäthyl eckige Klammer zu -N'-(4-chlorbenzhydril)- piperazin, dessen Salze, Verfahren zu deren Herstellung und pharmazeutische Zubereitung | |
| SU513973A1 (ru) | Способ получени 1-(3"-фенилпропен2"-ил)-2,5-диметил-4-фенил-4-пропионилоксипиперидина или его гидрохлорида | |
| SU372213A1 (ru) | Всесоюзная | |
| SU416356A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ 8-(р-АЛКИЛТИО) ЭТОКСИХИНОЛИНОВ | |
| DK147180B (da) | Fremgangsmaade til fremstilling af anilider af quinuclidin-carboxylsyre | |
| SU414258A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ ЧАСТИЧНО ГИДРИРОВАННЫХ N,N'-ДИAЦИJ]ЬHЫX ПРОИЗВОДНЫХдихинолилов и диизохинолилов |