WO2007025304A3 - Process for preparing saccharinic acids and lactones - Google Patents
Process for preparing saccharinic acids and lactones Download PDFInfo
- Publication number
- WO2007025304A3 WO2007025304A3 PCT/US2006/033736 US2006033736W WO2007025304A3 WO 2007025304 A3 WO2007025304 A3 WO 2007025304A3 US 2006033736 W US2006033736 W US 2006033736W WO 2007025304 A3 WO2007025304 A3 WO 2007025304A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- preparing
- lactones
- utilizes
- saccharinic acids
- saccharinic
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/26—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D307/30—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/32—Oxygen atoms
- C07D307/33—Oxygen atoms in position 2, the oxygen atom being in its keto or unsubstituted enol form
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Saccharide Compounds (AREA)
- Pyrane Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
An improved process for preparing a saccharinic acid or lactone is disclosed that utilizes the well-known Amadori rearrangement reaction. The synthesis utilizes protected or unprotected sugars or their analogues as starting materials, and reagents not previously utilized to afford increased product yields in decreased reaction time.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US71193405P | 2005-08-26 | 2005-08-26 | |
US60/711,934 | 2005-08-26 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2007025304A2 WO2007025304A2 (en) | 2007-03-01 |
WO2007025304A3 true WO2007025304A3 (en) | 2007-05-31 |
Family
ID=37772543
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2006/033736 WO2007025304A2 (en) | 2005-08-26 | 2006-08-28 | Process for preparing saccharinic acids and lactones |
Country Status (3)
Country | Link |
---|---|
AR (1) | AR057096A1 (en) |
UY (1) | UY29769A1 (en) |
WO (1) | WO2007025304A2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8299038B2 (en) | 2000-05-23 | 2012-10-30 | Idenix Pharmaceuticals, Inc. | Methods and compositions for treating hepatitis C virus |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ547204A (en) | 2000-05-26 | 2008-01-31 | Idenix Cayman Ltd | Methods and compositions for treating flaviviruses and pestiviruses |
HUE033832T2 (en) | 2002-11-15 | 2018-01-29 | Idenix Pharmaceuticals Llc | 2'-methyl nucleosides in combination with interferon and flaviviridae mutation |
JP5342887B2 (en) * | 2009-01-29 | 2013-11-13 | 花王株式会社 | Method for producing α-aminoketone compound |
US20150126752A1 (en) | 2012-06-13 | 2015-05-07 | Bristol-Myers Squibb Company | Process for the preparation of 2-c-methyl-d-ribonic-gamma-lactone |
CN104693157A (en) * | 2015-02-15 | 2015-06-10 | 上海应用技术学院 | Preparation method of 2-C-methyl-D-ribotide-1,4-lactone |
CN104693158B (en) * | 2015-02-15 | 2017-03-29 | 上海应用技术学院 | A kind of method for preparing 2 C methyl D ribonic acids, 1,4 lactone |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6891036B2 (en) * | 2003-02-10 | 2005-05-10 | Inalco S.P.A. | Process for the preparation of ribofuranose derivatives |
-
2006
- 2006-08-25 AR ARP060103721A patent/AR057096A1/en unknown
- 2006-08-28 WO PCT/US2006/033736 patent/WO2007025304A2/en active Application Filing
- 2006-08-28 UY UY29769A patent/UY29769A1/en not_active Application Discontinuation
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6891036B2 (en) * | 2003-02-10 | 2005-05-10 | Inalco S.P.A. | Process for the preparation of ribofuranose derivatives |
Non-Patent Citations (1)
Title |
---|
KUHN R. ET AL: "Uber eine molekulare Umlagerung von N-glucosiden", BERICHTE, vol. 69B, 1936, pages 1745 - 1754, XP008081654 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8299038B2 (en) | 2000-05-23 | 2012-10-30 | Idenix Pharmaceuticals, Inc. | Methods and compositions for treating hepatitis C virus |
Also Published As
Publication number | Publication date |
---|---|
WO2007025304A2 (en) | 2007-03-01 |
AR057096A1 (en) | 2007-11-14 |
UY29769A1 (en) | 2007-02-28 |
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