RU2566826C1 - Способ получения 1-пальмитоил-3-ацетилглицерина и способ получения 1-пальмитоил-2-линолеоил-3-ацетилглицерина с использованием этого соединения - Google Patents
Способ получения 1-пальмитоил-3-ацетилглицерина и способ получения 1-пальмитоил-2-линолеоил-3-ацетилглицерина с использованием этого соединения Download PDFInfo
- Publication number
- RU2566826C1 RU2566826C1 RU2014116232/04A RU2014116232A RU2566826C1 RU 2566826 C1 RU2566826 C1 RU 2566826C1 RU 2014116232/04 A RU2014116232/04 A RU 2014116232/04A RU 2014116232 A RU2014116232 A RU 2014116232A RU 2566826 C1 RU2566826 C1 RU 2566826C1
- Authority
- RU
- Russia
- Prior art keywords
- palmitoyl
- acetylglycerol
- linoleoyl
- amount
- acetylglycerine
- Prior art date
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- JJEYQTYWEVZYLY-UHFFFAOYSA-N (3-acetyloxy-2-hydroxypropyl) hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(O)COC(C)=O JJEYQTYWEVZYLY-UHFFFAOYSA-N 0.000 title claims abstract description 69
- 150000001875 compounds Chemical class 0.000 title claims abstract description 33
- GAKUNXBDVGLOFS-DUZKARGPSA-N (1-acetyloxy-3-hexadecanoyloxypropan-2-yl) (9z,12z)-octadeca-9,12-dienoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(COC(C)=O)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC GAKUNXBDVGLOFS-DUZKARGPSA-N 0.000 title claims abstract description 31
- 238000000034 method Methods 0.000 title claims abstract description 25
- 239000011541 reaction mixture Substances 0.000 claims abstract description 30
- QHZLMUACJMDIAE-UHFFFAOYSA-N 1-monopalmitoylglycerol Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(O)CO QHZLMUACJMDIAE-UHFFFAOYSA-N 0.000 claims abstract description 29
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 claims abstract description 28
- 239000002904 solvent Substances 0.000 claims abstract description 19
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 claims abstract description 17
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 claims abstract description 17
- 235000020778 linoleic acid Nutrition 0.000 claims abstract description 17
- JVSFQJZRHXAUGT-UHFFFAOYSA-N 2,2-dimethylpropanoyl chloride Chemical compound CC(C)(C)C(Cl)=O JVSFQJZRHXAUGT-UHFFFAOYSA-N 0.000 claims abstract description 15
- 150000007530 organic bases Chemical class 0.000 claims abstract description 15
- 150000008064 anhydrides Chemical class 0.000 claims abstract description 14
- 229930195734 saturated hydrocarbon Natural products 0.000 claims abstract description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 9
- GAKUNXBDVGLOFS-UHFFFAOYSA-N PLA Natural products CCCCCCCCCCCCCCCC(=O)OCC(COC(C)=O)OC(=O)CCCCCCCC=CCC=CCCCCC GAKUNXBDVGLOFS-UHFFFAOYSA-N 0.000 claims description 22
- 238000004519 manufacturing process Methods 0.000 claims description 15
- 239000012345 acetylating agent Substances 0.000 claims description 13
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical group CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- 239000003495 polar organic solvent Substances 0.000 claims description 9
- 238000002425 crystallisation Methods 0.000 claims description 8
- 230000008025 crystallization Effects 0.000 claims description 8
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 claims description 4
- 239000012346 acetyl chloride Substances 0.000 claims description 4
- FXXACINHVKSMDR-UHFFFAOYSA-N acetyl bromide Chemical compound CC(Br)=O FXXACINHVKSMDR-UHFFFAOYSA-N 0.000 claims description 3
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 claims description 2
- 238000004440 column chromatography Methods 0.000 abstract description 13
- 238000000746 purification Methods 0.000 abstract description 13
- 238000006640 acetylation reaction Methods 0.000 abstract description 12
- 230000021736 acetylation Effects 0.000 abstract description 5
- 230000000694 effects Effects 0.000 abstract description 3
- 239000003795 chemical substances by application Substances 0.000 abstract 4
- 239000003960 organic solvent Substances 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 45
- 238000006243 chemical reaction Methods 0.000 description 25
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 15
- 239000006227 byproduct Substances 0.000 description 12
- 230000008901 benefit Effects 0.000 description 10
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
- CIUYPOUJRYWLDF-UHFFFAOYSA-N 2,3-diacetyloxypropyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(OC(C)=O)COC(C)=O CIUYPOUJRYWLDF-UHFFFAOYSA-N 0.000 description 8
- RZSWZKFNJCIAQR-UHFFFAOYSA-N (2-acetyloxy-3-hydroxypropyl) hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(CO)OC(C)=O RZSWZKFNJCIAQR-UHFFFAOYSA-N 0.000 description 7
- 125000004185 ester group Chemical group 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 230000035484 reaction time Effects 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 3
- JJEYQTYWEVZYLY-HXUWFJFHSA-N [(2r)-3-acetyloxy-2-hydroxypropyl] hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](O)COC(C)=O JJEYQTYWEVZYLY-HXUWFJFHSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- IXCSERBJSXMMFS-UHFFFAOYSA-N hcl hcl Chemical compound Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
- 238000002955 isolation Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 125000006239 protecting group Chemical group 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- 206010067484 Adverse reaction Diseases 0.000 description 2
- 241000282994 Cervidae Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- GAKUNXBDVGLOFS-WCCXBCNRSA-N [(2r)-1-acetyloxy-3-hexadecanoyloxypropan-2-yl] (9z,12z)-octadeca-9,12-dienoate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](COC(C)=O)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC GAKUNXBDVGLOFS-WCCXBCNRSA-N 0.000 description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical group 0.000 description 2
- 230000006838 adverse reaction Effects 0.000 description 2
- 210000003056 antler Anatomy 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000002860 competitive effect Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 150000002314 glycerols Chemical class 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- RPOLZUSVGJWCKY-DUZKARGPSA-N (2-acetyloxy-3-hexadecanoyloxypropyl) (9z,12z)-octadeca-9,12-dienoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(OC(C)=O)COC(=O)CCCCCCC\C=C/C\C=C/CCCCC RPOLZUSVGJWCKY-DUZKARGPSA-N 0.000 description 1
- ADFXKUOMJKEIND-UHFFFAOYSA-N 1,3-dicyclohexylurea Chemical compound C1CCCCC1NC(=O)NC1CCCCC1 ADFXKUOMJKEIND-UHFFFAOYSA-N 0.000 description 1
- QHZLMUACJMDIAE-GOSISDBHSA-N 3-palmitoyl-sn-glycerol Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](O)CO QHZLMUACJMDIAE-GOSISDBHSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 238000005741 Steglich esterification reaction Methods 0.000 description 1
- 238000005852 acetolysis reaction Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000002026 chloroform extract Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 210000003958 hematopoietic stem cell Anatomy 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 210000003593 megakaryocyte Anatomy 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- LSCYTCMNCWMCQE-UHFFFAOYSA-N n-methylpyridin-4-amine Chemical compound CNC1=CC=NC=C1 LSCYTCMNCWMCQE-UHFFFAOYSA-N 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- WTJKGGKOPKCXLL-RRHRGVEJSA-N phosphatidylcholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCCCC WTJKGGKOPKCXLL-RRHRGVEJSA-N 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/08—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/307—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by introduction of halogen; by substitution of halogen atoms by other halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B57/00—Separation of optically-active compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/10—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with ester groups or with a carbon-halogen bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/14—Preparation of carboxylic acid esters from carboxylic acid halides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/48—Separation; Purification; Stabilisation; Use of additives
- C07C67/52—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
- C07C69/22—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety
- C07C69/30—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety esterified with trihydroxylic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/34—Esters of acyclic saturated polycarboxylic acids having an esterified carboxyl group bound to an acyclic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1020110096341A KR101278874B1 (ko) | 2011-09-23 | 2011-09-23 | 1-팔미토일-3-아세틸글리세롤의 제조방법 및 이를 이용한 1-팔미토일-2-리놀레오일-3-아세틸글리세롤의 제조방법 |
| KR10-2011-0096341 | 2011-09-23 | ||
| PCT/KR2012/007644 WO2013043009A2 (ko) | 2011-09-23 | 2012-09-24 | 1-팔미토일-3-아세틸글리세롤의 제조방법 및 이를 이용한 1-팔미토일-2-리놀레오일-3-아세틸글리세롤의 제조방법 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2566826C1 true RU2566826C1 (ru) | 2015-10-27 |
Family
ID=47915041
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2014116232/04A RU2566826C1 (ru) | 2011-09-23 | 2012-09-24 | Способ получения 1-пальмитоил-3-ацетилглицерина и способ получения 1-пальмитоил-2-линолеоил-3-ацетилглицерина с использованием этого соединения |
Country Status (11)
| Country | Link |
|---|---|
| US (3) | US20140243548A1 (enExample) |
| EP (1) | EP2759529B1 (enExample) |
| JP (1) | JP5799171B2 (enExample) |
| KR (1) | KR101278874B1 (enExample) |
| CN (1) | CN103827075B (enExample) |
| AU (1) | AU2012310342B2 (enExample) |
| CA (1) | CA2849289C (enExample) |
| ES (1) | ES2620103T3 (enExample) |
| IN (1) | IN2014DN02166A (enExample) |
| RU (1) | RU2566826C1 (enExample) |
| WO (1) | WO2013043009A2 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2758793C1 (ru) * | 2021-03-29 | 2021-11-01 | Федеральное Государственное Бюджетное Образовательное Учреждение Высшего Образования «Новосибирский Государственный Технический Университет» | Адаптивная стартер-генераторная система |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101278874B1 (ko) | 2011-09-23 | 2013-06-26 | 주식회사 엔지켐생명과학 | 1-팔미토일-3-아세틸글리세롤의 제조방법 및 이를 이용한 1-팔미토일-2-리놀레오일-3-아세틸글리세롤의 제조방법 |
| RU2636615C2 (ru) * | 2013-08-19 | 2017-11-24 | Энзикем Лайфсайенсиз Корпорейшн | Композиция для предотвращения или лечения астмы, содержащая моноацетилдиацилглицериновое соединение в качестве активного ингредиента |
| US9808438B2 (en) | 2015-11-09 | 2017-11-07 | Enzychem Lifesciences Corporation | Method for treating mucositis |
| US10653657B2 (en) | 2015-11-14 | 2020-05-19 | Enzychem Lifesciences Corporation | Method for treating hemolytic uremic syndrome |
| WO2017082708A1 (ko) | 2015-11-14 | 2017-05-18 | 주식회사 엔지켐생명과학 | 발작성 야간 혈색소뇨증의 치료 방법 |
| IL274974B2 (en) | 2017-11-30 | 2025-03-01 | Enzychem Lifesciences Corp | Compositions for prevention or treatment of acute radiation syndrome |
| KR102333606B1 (ko) * | 2019-10-15 | 2021-12-01 | 주식회사 엔지켐생명과학 | 1-팔미토일-2-리놀레오일-3-아세틸 글리세롤의 제조 방법 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2341257C2 (ru) * | 2004-04-24 | 2008-12-20 | Санг-Хи КИМ | Иммуномодулирующее средство, противораковое средство и здоровая пища, содержащая производные моноацетилдиацилглицерина |
| US7868196B2 (en) * | 2005-07-20 | 2011-01-11 | Enzychem Co., Ltd. | Preparation of glycerol derivatives and intermediates therefor |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0694438B2 (ja) * | 1985-11-06 | 1994-11-24 | 株式会社ツムラ | 新規なグリセリン誘導体 |
| JPH0694438A (ja) | 1992-09-14 | 1994-04-05 | Matsushita Electric Works Ltd | 光切断法による外観検査装置 |
| JP3408337B2 (ja) * | 1994-10-05 | 2003-05-19 | 花王株式会社 | グリセリン誘導体の製造法 |
| JPH09110787A (ja) * | 1995-10-11 | 1997-04-28 | Hoechst Japan Ltd | 無溶媒反応による１級アルコールとフェノールのアセチル化方法 |
| DK0847994T3 (da) * | 1996-12-11 | 2003-07-28 | Hoffmann La Roche | Fremgangsmåde til fremstilling af blandede anhydrider |
| KR100291743B1 (ko) | 1997-11-20 | 2001-05-15 | 전길자 | 글리세롤 유도체의 제조방법 |
| DE69833333T2 (de) * | 1997-11-20 | 2006-10-19 | Jhon, Gil Ja | Pharmazeutische zusammensetzung enthaltend geweihextrakte von cervus nippon mit wachstumsstimulierender aktivität auf hematopoietische stammzellen und megakaryozyten |
| KR100283010B1 (ko) | 1997-11-20 | 2001-04-02 | 전길자 | 녹용 추출물을 함유하는 조혈모세포 및 혈소판 전구세포 증식촉진용 조성물 |
| KR20010008387A (ko) * | 2000-11-30 | 2001-02-05 | 이성권 | 결정화방법을 이용한 고순도 불포화지방산의 분리 정제 방법 |
| KR100754888B1 (ko) * | 2004-03-22 | 2007-09-04 | 주식회사 엔지켐 | 글리세롤 유도체의 위치 선택적인 제조방법 및 그 중간체 |
| WO2010006261A1 (en) * | 2008-07-10 | 2010-01-14 | Hong John J | Methods for inducing stem cell migration and specialization with ec-18 |
| KR101278874B1 (ko) | 2011-09-23 | 2013-06-26 | 주식회사 엔지켐생명과학 | 1-팔미토일-3-아세틸글리세롤의 제조방법 및 이를 이용한 1-팔미토일-2-리놀레오일-3-아세틸글리세롤의 제조방법 |
| JP6094438B2 (ja) | 2013-09-27 | 2017-03-15 | トヨタ自動車株式会社 | 内燃機関の制御装置 |
-
2011
- 2011-09-23 KR KR1020110096341A patent/KR101278874B1/ko active Active
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2012
- 2012-09-24 EP EP12834214.4A patent/EP2759529B1/en active Active
- 2012-09-24 WO PCT/KR2012/007644 patent/WO2013043009A2/ko not_active Ceased
- 2012-09-24 JP JP2014531727A patent/JP5799171B2/ja active Active
- 2012-09-24 CA CA2849289A patent/CA2849289C/en active Active
- 2012-09-24 RU RU2014116232/04A patent/RU2566826C1/ru active
- 2012-09-24 US US14/346,783 patent/US20140243548A1/en not_active Abandoned
- 2012-09-24 IN IN2166DEN2014 patent/IN2014DN02166A/en unknown
- 2012-09-24 CN CN201280046277.7A patent/CN103827075B/zh active Active
- 2012-09-24 AU AU2012310342A patent/AU2012310342B2/en active Active
- 2012-09-24 ES ES12834214.4T patent/ES2620103T3/es active Active
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| RU2341257C2 (ru) * | 2004-04-24 | 2008-12-20 | Санг-Хи КИМ | Иммуномодулирующее средство, противораковое средство и здоровая пища, содержащая производные моноацетилдиацилглицерина |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2758793C1 (ru) * | 2021-03-29 | 2021-11-01 | Федеральное Государственное Бюджетное Образовательное Учреждение Высшего Образования «Новосибирский Государственный Технический Университет» | Адаптивная стартер-генераторная система |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20130032628A (ko) | 2013-04-02 |
| US9701613B2 (en) | 2017-07-11 |
| CA2849289A1 (en) | 2013-03-28 |
| US20170183287A1 (en) | 2017-06-29 |
| JP2014528945A (ja) | 2014-10-30 |
| EP2759529A2 (en) | 2014-07-30 |
| US20140243548A1 (en) | 2014-08-28 |
| WO2013043009A3 (ko) | 2013-05-30 |
| US20160083329A1 (en) | 2016-03-24 |
| AU2012310342B2 (en) | 2015-11-26 |
| KR101278874B1 (ko) | 2013-06-26 |
| AU2012310342A1 (en) | 2014-04-03 |
| ES2620103T3 (es) | 2017-06-27 |
| EP2759529A4 (en) | 2015-05-20 |
| CA2849289C (en) | 2016-05-10 |
| WO2013043009A2 (ko) | 2013-03-28 |
| EP2759529B1 (en) | 2016-12-21 |
| IN2014DN02166A (enExample) | 2015-05-15 |
| CN103827075A (zh) | 2014-05-28 |
| JP5799171B2 (ja) | 2015-10-21 |
| CN103827075B (zh) | 2015-09-16 |
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