NO323684B1 - Fremgangsmate for fremstilling av perbenzylerte 1-O-glykosider - Google Patents
Fremgangsmate for fremstilling av perbenzylerte 1-O-glykosider Download PDFInfo
- Publication number
- NO323684B1 NO323684B1 NO20024290A NO20024290A NO323684B1 NO 323684 B1 NO323684 B1 NO 323684B1 NO 20024290 A NO20024290 A NO 20024290A NO 20024290 A NO20024290 A NO 20024290A NO 323684 B1 NO323684 B1 NO 323684B1
- Authority
- NO
- Norway
- Prior art keywords
- residue
- mmol
- perbenzylated
- general formula
- sugar
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 33
- 238000002360 preparation method Methods 0.000 title claims description 9
- 150000002772 monosaccharides Chemical class 0.000 claims abstract description 10
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 6
- 150000003839 salts Chemical class 0.000 claims abstract description 6
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- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 47
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- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 32
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 32
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- 125000006239 protecting group Chemical group 0.000 claims description 17
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- SHZGCJCMOBCMKK-UHFFFAOYSA-N D-mannomethylose Natural products CC1OC(O)C(O)C(O)C1O SHZGCJCMOBCMKK-UHFFFAOYSA-N 0.000 claims description 6
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 claims description 6
- 238000005804 alkylation reaction Methods 0.000 claims description 6
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 claims description 6
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 claims description 6
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- 230000002152 alkylating effect Effects 0.000 claims description 5
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims description 5
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- SHZGCJCMOBCMKK-JFNONXLTSA-N L-rhamnopyranose Chemical compound C[C@@H]1OC(O)[C@H](O)[C@H](O)[C@H]1O SHZGCJCMOBCMKK-JFNONXLTSA-N 0.000 claims description 4
- 239000003444 phase transfer catalyst Substances 0.000 claims description 4
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- HMFHBZSHGGEWLO-SOOFDHNKSA-N D-ribofuranose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@@H]1O HMFHBZSHGGEWLO-SOOFDHNKSA-N 0.000 claims description 3
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- 230000029936 alkylation Effects 0.000 claims description 3
- HMFHBZSHGGEWLO-UHFFFAOYSA-N alpha-D-Furanose-Ribose Natural products OCC1OC(O)C(O)C1O HMFHBZSHGGEWLO-UHFFFAOYSA-N 0.000 claims description 3
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 3
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 claims description 3
- 125000001153 fluoro group Chemical group F* 0.000 claims description 3
- 229930182830 galactose Natural products 0.000 claims description 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 3
- 125000004434 sulfur atom Chemical group 0.000 claims description 3
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 2
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 150000003983 crown ethers Chemical class 0.000 claims description 2
- 150000004714 phosphonium salts Chemical class 0.000 claims description 2
- 150000001720 carbohydrates Chemical class 0.000 abstract description 8
- 238000004519 manufacturing process Methods 0.000 abstract description 5
- 239000007858 starting material Substances 0.000 abstract description 4
- 229930182470 glycoside Natural products 0.000 abstract description 3
- 150000002338 glycosides Chemical class 0.000 abstract description 3
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- CZMRCDWAGMRECN-UHFFFAOYSA-N 2-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound OCC1OC(CO)(OC2OC(CO)C(O)C(O)C2O)C(O)C1O CZMRCDWAGMRECN-UHFFFAOYSA-N 0.000 abstract 1
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- 238000011031 large-scale manufacturing process Methods 0.000 abstract 1
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- 239000012074 organic phase Substances 0.000 description 55
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 52
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- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 36
- 238000003756 stirring Methods 0.000 description 36
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- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 26
- NHGXDBSUJJNIRV-UHFFFAOYSA-M tetrabutylammonium chloride Chemical compound [Cl-].CCCC[N+](CCCC)(CCCC)CCCC NHGXDBSUJJNIRV-UHFFFAOYSA-M 0.000 description 22
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- FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 description 8
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- 125000005982 diphenylmethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
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- ZFAMQJATRWOMHH-UHFFFAOYSA-N ethyl 3-bromo-2-phenylpropanoate Chemical compound CCOC(=O)C(CBr)C1=CC=CC=C1 ZFAMQJATRWOMHH-UHFFFAOYSA-N 0.000 description 1
- ALPFIWHKOHBYEF-UHFFFAOYSA-N ethyl 4-(3-methylsulfonyloxypropyl)benzoate Chemical compound CCOC(=O)C1=CC=C(CCCOS(C)(=O)=O)C=C1 ALPFIWHKOHBYEF-UHFFFAOYSA-N 0.000 description 1
- DXBULVYHTICWKT-UHFFFAOYSA-N ethyl 6-bromohexanoate Chemical compound CCOC(=O)CCCCCBr DXBULVYHTICWKT-UHFFFAOYSA-N 0.000 description 1
- PQJJJMRNHATNKG-UHFFFAOYSA-N ethyl bromoacetate Chemical compound CCOC(=O)CBr PQJJJMRNHATNKG-UHFFFAOYSA-N 0.000 description 1
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- 239000013067 intermediate product Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
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- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- DTBGILDKBIBTGE-UHFFFAOYSA-N n-(1-hydroxyethyl)formamide Chemical compound CC(O)NC=O DTBGILDKBIBTGE-UHFFFAOYSA-N 0.000 description 1
- XRRCVJUSXHXUHS-UHFFFAOYSA-N n-(4-bromobutyl)-2-trimethylsilylethanesulfonamide Chemical compound C[Si](C)(C)CCS(=O)(=O)NCCCCBr XRRCVJUSXHXUHS-UHFFFAOYSA-N 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 125000006503 p-nitrobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1[N+]([O-])=O)C([H])([H])* 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 150000002972 pentoses Chemical class 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
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- 230000035484 reaction time Effects 0.000 description 1
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- 238000011069 regeneration method Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000013341 scale-up Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- KUOSNTKAZFIQSS-UHFFFAOYSA-N tert-butyl 6-(4-methylphenyl)sulfonyloxyhexanoate Chemical compound CC1=CC=C(S(=O)(=O)OCCCCCC(=O)OC(C)(C)C)C=C1 KUOSNTKAZFIQSS-UHFFFAOYSA-N 0.000 description 1
- 125000000037 tert-butyldiphenylsilyl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1[Si]([H])([*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000004043 trisaccharides Chemical class 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- CITILBVTAYEWKR-UHFFFAOYSA-L zinc trifluoromethanesulfonate Chemical compound [Zn+2].[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F CITILBVTAYEWKR-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/20—Carbocyclic rings
- C07H15/203—Monocyclic carbocyclic rings other than cyclohexane rings; Bicyclic carbocyclic ring 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)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10013328A DE10013328C2 (de) | 2000-03-10 | 2000-03-10 | Verfahren zur Herstellung von perbenzylierten 1-O-Glycosiden |
| PCT/EP2001/002024 WO2001068659A2 (de) | 2000-03-10 | 2001-02-22 | Verfahren zur herstellung von perbenzylierten 1-o-glycosiden |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO20024290D0 NO20024290D0 (no) | 2002-09-09 |
| NO20024290L NO20024290L (no) | 2002-09-09 |
| NO323684B1 true NO323684B1 (no) | 2007-06-25 |
Family
ID=7635315
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20024290A NO323684B1 (no) | 2000-03-10 | 2002-09-09 | Fremgangsmate for fremstilling av perbenzylerte 1-O-glykosider |
Country Status (9)
| Country | Link |
|---|---|
| EP (1) | EP1261614B1 (ja) |
| JP (1) | JP2003527397A (ja) |
| AT (1) | ATE257483T1 (ja) |
| AU (1) | AU2001254659A1 (ja) |
| DE (2) | DE10013328C2 (ja) |
| DK (1) | DK1261614T3 (ja) |
| ES (1) | ES2213692T3 (ja) |
| NO (1) | NO323684B1 (ja) |
| WO (1) | WO2001068659A2 (ja) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6545135B2 (en) * | 2000-03-10 | 2003-04-08 | Schering Aktiengesellschaft | Process for the production of perbenzylated 1-O-glycosides |
| DE10129677C2 (de) * | 2001-06-18 | 2003-10-16 | Schering Ag | Verfahren zur Herstellung von perbenzylierten 1-O-Glycosiden |
| DE10129888C2 (de) * | 2001-06-19 | 2003-10-16 | Schering Ag | Verfahren zur Herstellung von perbenzylierten 1-O-Glycosiden |
| US6831164B2 (en) | 2001-07-11 | 2004-12-14 | Schering Aktiengesellschaft | Process for the production of peracylated 1-0-glycosides |
| DE10135098B4 (de) * | 2001-07-11 | 2004-05-13 | Schering Ag | Verfahren zur Herstellung von peracylierten 1-O-Glycosiden |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU1122897A (en) * | 1995-11-13 | 1997-06-05 | Glycomed Incorporated | Novel oligosaccharide glycosides having mammalian immunosuppressive and tolerogenic properties |
| JP3816570B2 (ja) * | 1996-02-16 | 2006-08-30 | 塩水港精糖株式会社 | アシル化剤 |
-
2000
- 2000-03-10 DE DE10013328A patent/DE10013328C2/de not_active Expired - Fee Related
-
2001
- 2001-02-22 DK DK01927688T patent/DK1261614T3/da active
- 2001-02-22 ES ES01927688T patent/ES2213692T3/es not_active Expired - Lifetime
- 2001-02-22 WO PCT/EP2001/002024 patent/WO2001068659A2/de active IP Right Grant
- 2001-02-22 EP EP01927688A patent/EP1261614B1/de not_active Expired - Lifetime
- 2001-02-22 JP JP2001567749A patent/JP2003527397A/ja not_active Withdrawn
- 2001-02-22 AT AT01927688T patent/ATE257483T1/de not_active IP Right Cessation
- 2001-02-22 AU AU2001254659A patent/AU2001254659A1/en not_active Abandoned
- 2001-02-22 DE DE50101293T patent/DE50101293D1/de not_active Expired - Fee Related
-
2002
- 2002-09-09 NO NO20024290A patent/NO323684B1/no unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DK1261614T3 (da) | 2004-04-26 |
| ATE257483T1 (de) | 2004-01-15 |
| JP2003527397A (ja) | 2003-09-16 |
| DE10013328C2 (de) | 2002-12-19 |
| EP1261614A2 (de) | 2002-12-04 |
| DE10013328A1 (de) | 2001-09-20 |
| NO20024290D0 (no) | 2002-09-09 |
| DE50101293D1 (de) | 2004-02-12 |
| EP1261614B1 (de) | 2004-01-07 |
| WO2001068659A2 (de) | 2001-09-20 |
| WO2001068659A3 (de) | 2001-12-20 |
| AU2001254659A1 (en) | 2001-09-24 |
| NO20024290L (no) | 2002-09-09 |
| ES2213692T3 (es) | 2004-09-01 |
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