SU457213A3 - Способ получени сложных эфиров м-тирозина - Google Patents
Способ получени сложных эфиров м-тирозинаInfo
- Publication number
- SU457213A3 SU457213A3 SU1796209A SU1796209A SU457213A3 SU 457213 A3 SU457213 A3 SU 457213A3 SU 1796209 A SU1796209 A SU 1796209A SU 1796209 A SU1796209 A SU 1796209A SU 457213 A3 SU457213 A3 SU 457213A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- tyrosine
- producing
- ester
- tyrosine esters
- esters
- Prior art date
Links
- JZKXXXDKRQWDET-QMMMGPOBSA-N L-m-tyrosine Chemical class OC(=O)[C@@H](N)CC1=CC=CC(O)=C1 JZKXXXDKRQWDET-QMMMGPOBSA-N 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 150000003839 salts Chemical class 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- MIOPJNTWMNEORI-GMSGAONNSA-N (S)-camphorsulfonic acid Chemical compound C1C[C@@]2(CS(O)(=O)=O)C(=O)C[C@@H]1C2(C)C MIOPJNTWMNEORI-GMSGAONNSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium on carbon Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- QOSMNYMQXIVWKY-UHFFFAOYSA-N Propyl levulinate Chemical compound CCCOC(=O)CCC(C)=O QOSMNYMQXIVWKY-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- ROBXZHNBBCHEIQ-BYPYZUCNSA-N ethyl (2s)-2-aminopropanoate Chemical compound CCOC(=O)[C@H](C)N ROBXZHNBBCHEIQ-BYPYZUCNSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- -1 for example Substances 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- RXTAVOMESVSQHO-UHFFFAOYSA-N propyl 2-amino-3-(4-hydroxyphenyl)propanoate Chemical compound CCCOC(=O)C(N)CC1=CC=C(O)C=C1 RXTAVOMESVSQHO-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
Landscapes
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE03142/70A SE353528B (enExample) | 1970-03-10 | 1970-03-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU457213A3 true SU457213A3 (ru) | 1975-01-15 |
Family
ID=20261468
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1796209A SU457213A3 (ru) | 1970-03-10 | 1971-03-05 | Способ получени сложных эфиров м-тирозина |
| SU1627790A SU403163A3 (enExample) | 1970-03-10 | 1971-03-05 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1627790A SU403163A3 (enExample) | 1970-03-10 | 1971-03-05 |
Country Status (13)
| Country | Link |
|---|---|
| AT (1) | AT307390B (enExample) |
| BE (1) | BE763773A (enExample) |
| CA (1) | CA933179A (enExample) |
| DE (1) | DE2109657C3 (enExample) |
| ES (3) | ES388844A1 (enExample) |
| FR (1) | FR2085691B1 (enExample) |
| GB (1) | GB1315234A (enExample) |
| IE (1) | IE34996B1 (enExample) |
| NL (1) | NL7103099A (enExample) |
| NO (1) | NO132091C (enExample) |
| SE (1) | SE353528B (enExample) |
| SU (2) | SU457213A3 (enExample) |
| ZA (1) | ZA711121B (enExample) |
-
1970
- 1970-03-10 SE SE03142/70A patent/SE353528B/xx unknown
-
1971
- 1971-02-22 ZA ZA711121A patent/ZA711121B/xx unknown
- 1971-03-01 DE DE2109657A patent/DE2109657C3/de not_active Expired
- 1971-03-03 ES ES388844A patent/ES388844A1/es not_active Expired
- 1971-03-04 BE BE763773A patent/BE763773A/xx unknown
- 1971-03-05 SU SU1796209A patent/SU457213A3/ru active
- 1971-03-05 SU SU1627790A patent/SU403163A3/ru active
- 1971-03-08 AT AT194571A patent/AT307390B/de not_active IP Right Cessation
- 1971-03-09 NL NL7103099A patent/NL7103099A/xx unknown
- 1971-03-09 IE IE294/71A patent/IE34996B1/xx unknown
- 1971-03-09 NO NO893/71A patent/NO132091C/no unknown
- 1971-03-09 FR FR7108137A patent/FR2085691B1/fr not_active Expired
- 1971-03-10 CA CA107341A patent/CA933179A/en not_active Expired
- 1971-04-19 GB GB2353471*A patent/GB1315234A/en not_active Expired
-
1972
- 1972-02-12 ES ES399726A patent/ES399726A1/es not_active Expired
- 1972-02-12 ES ES399725A patent/ES399725A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| NO132091B (enExample) | 1975-06-09 |
| FR2085691A1 (enExample) | 1971-12-31 |
| DE2109657C3 (de) | 1976-01-02 |
| NL7103099A (enExample) | 1971-09-14 |
| IE34996L (en) | 1971-09-10 |
| ZA711121B (en) | 1971-11-24 |
| ES399725A1 (es) | 1974-11-16 |
| ES399726A1 (es) | 1974-11-16 |
| DE2109657A1 (de) | 1971-09-23 |
| BE763773A (fr) | 1971-08-02 |
| AT307390B (de) | 1973-05-25 |
| DE2109657B2 (de) | 1975-05-22 |
| NO132091C (enExample) | 1975-09-17 |
| SU403163A3 (enExample) | 1973-10-19 |
| SE353528B (enExample) | 1973-02-05 |
| FR2085691B1 (enExample) | 1975-06-06 |
| GB1315234A (en) | 1973-05-02 |
| IE34996B1 (en) | 1975-10-15 |
| CA933179A (en) | 1973-09-04 |
| ES388844A1 (es) | 1974-03-01 |
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