CN101012252A - 1,2,3-三-o-乙酰基-5-脱氧-d-核糖合成方法 - Google Patents
1,2,3-三-o-乙酰基-5-脱氧-d-核糖合成方法 Download PDFInfo
- Publication number
- CN101012252A CN101012252A CNA2007100198737A CN200710019873A CN101012252A CN 101012252 A CN101012252 A CN 101012252A CN A2007100198737 A CNA2007100198737 A CN A2007100198737A CN 200710019873 A CN200710019873 A CN 200710019873A CN 101012252 A CN101012252 A CN 101012252A
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- ethanoyl
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Links
- 238000000034 method Methods 0.000 title abstract description 4
- 230000002194 synthesizing effect Effects 0.000 title abstract 2
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 claims abstract description 42
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims abstract description 18
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 8
- 239000002994 raw material Substances 0.000 claims abstract description 8
- 239000002904 solvent Substances 0.000 claims abstract description 7
- 239000007791 liquid phase Substances 0.000 claims abstract description 6
- 239000011347 resin Substances 0.000 claims abstract description 6
- 229920005989 resin Polymers 0.000 claims abstract description 6
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000011630 iodine Substances 0.000 claims abstract description 5
- 229910052740 iodine Inorganic materials 0.000 claims abstract description 5
- 239000003960 organic solvent Substances 0.000 claims abstract description 5
- 239000013067 intermediate product Substances 0.000 claims description 45
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 30
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 18
- 238000002360 preparation method Methods 0.000 claims description 15
- 238000006243 chemical reaction Methods 0.000 claims description 13
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 claims description 12
- 229960003786 inosine Drugs 0.000 claims description 11
- 238000010189 synthetic method Methods 0.000 claims description 11
- 239000000047 product Substances 0.000 claims description 10
- 229930010555 Inosine Natural products 0.000 claims description 9
- UGQMRVRMYYASKQ-KQYNXXCUSA-N Inosine Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C2=NC=NC(O)=C2N=C1 UGQMRVRMYYASKQ-KQYNXXCUSA-N 0.000 claims description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 9
- 239000013078 crystal Substances 0.000 claims description 8
- 238000002425 crystallisation Methods 0.000 claims description 7
- 150000002460 imidazoles Chemical class 0.000 claims description 6
- 238000000926 separation method Methods 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 239000000706 filtrate Substances 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 239000000243 solution Substances 0.000 claims description 5
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 4
- 230000002378 acidificating effect Effects 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 4
- 230000008025 crystallization Effects 0.000 claims description 4
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 4
- 150000002500 ions Chemical class 0.000 claims description 4
- -1 sulfurous acid saturated brine Chemical class 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 230000000694 effects Effects 0.000 claims description 3
- 239000012046 mixed solvent Substances 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 3
- 238000010504 bond cleavage reaction Methods 0.000 claims description 2
- 239000012141 concentrate Substances 0.000 claims description 2
- 238000001914 filtration Methods 0.000 claims description 2
- 230000008014 freezing Effects 0.000 claims description 2
- 238000007710 freezing Methods 0.000 claims description 2
- 229930182470 glycoside Natural products 0.000 claims description 2
- 150000002338 glycosides Chemical class 0.000 claims description 2
- 238000010992 reflux Methods 0.000 claims description 2
- 230000007017 scission Effects 0.000 claims description 2
- 238000005406 washing Methods 0.000 claims description 2
- 239000007806 chemical reaction intermediate Substances 0.000 claims 1
- 239000002893 slag Substances 0.000 claims 1
- 239000002253 acid Substances 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 150000001768 cations Chemical class 0.000 abstract 1
- 239000002131 composite material Substances 0.000 abstract 1
- 229920002477 rna polymer Polymers 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 description 7
- 238000001514 detection method Methods 0.000 description 5
- 239000003814 drug Substances 0.000 description 3
- 125000003147 glycosyl group Chemical group 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 239000002777 nucleoside Substances 0.000 description 2
- 150000003833 nucleoside derivatives Chemical class 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 230000010933 acylation Effects 0.000 description 1
- 238000005917 acylation reaction Methods 0.000 description 1
- 230000000259 anti-tumor effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- ICIWUVCWSCSTAQ-UHFFFAOYSA-M iodate Chemical compound [O-]I(=O)=O ICIWUVCWSCSTAQ-UHFFFAOYSA-M 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010977 unit operation Methods 0.000 description 1
- 238000004148 unit process Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
- C07H13/02—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids
- C07H13/04—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids having the esterifying carboxyl radicals attached to acyclic carbon atoms
- C07H13/06—Fatty acids
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- 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)
- Catalysts (AREA)
Abstract
Description
Claims (5)
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2007100198737A CN100432088C (zh) | 2007-01-30 | 2007-01-30 | 1,2,3-三-o-乙酰基-5-脱氧-d-核糖合成方法 |
PCT/CN2008/070190 WO2008092405A1 (fr) | 2007-01-30 | 2008-01-25 | Procédé de synthèse du 1,2,3-tri-o-acétyl-5-désoxy-d-ribose |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2007100198737A CN100432088C (zh) | 2007-01-30 | 2007-01-30 | 1,2,3-三-o-乙酰基-5-脱氧-d-核糖合成方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN101012252A true CN101012252A (zh) | 2007-08-08 |
CN100432088C CN100432088C (zh) | 2008-11-12 |
Family
ID=38699993
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB2007100198737A Expired - Fee Related CN100432088C (zh) | 2007-01-30 | 2007-01-30 | 1,2,3-三-o-乙酰基-5-脱氧-d-核糖合成方法 |
Country Status (2)
Country | Link |
---|---|
CN (1) | CN100432088C (zh) |
WO (1) | WO2008092405A1 (zh) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008092405A1 (fr) * | 2007-01-30 | 2008-08-07 | Donglin Tang | Procédé de synthèse du 1,2,3-tri-o-acétyl-5-désoxy-d-ribose |
WO2009044886A1 (ja) | 2007-10-05 | 2009-04-09 | Api Corporation | リボフラノース誘導体の製造方法 |
CN101993463A (zh) * | 2009-08-19 | 2011-03-30 | 成都康弘药业集团股份有限公司 | 一种卡培他滨及其中间体的制备方法 |
CN102432642A (zh) * | 2011-10-17 | 2012-05-02 | 江西科技师范学院 | 1, 2, 3-o-三乙酰基-5-脱氧-d-呋喃核糖的合成方法 |
CN103772450A (zh) * | 2012-10-18 | 2014-05-07 | 黑龙江福和华星制药集团股份有限公司 | 一种1,2,3-三乙酰基-5-脱氧-d-核糖的制法 |
CN104650160A (zh) * | 2015-01-13 | 2015-05-27 | 济南大学 | 卡培他滨关键中间体1,2,3-o-三乙酰基-5-脱氧-d-核糖的合成新方法 |
CN103897005B (zh) * | 2012-12-27 | 2017-07-28 | 鲁南制药集团股份有限公司 | 一种连续操作合成卡培他滨的方法 |
CN107118241A (zh) * | 2017-05-03 | 2017-09-01 | 南京信息工程大学 | 一种6‑硝基‑脱氧‑三乙酰基甲基葡萄糖苷的制备方法 |
CN107827938A (zh) * | 2017-10-27 | 2018-03-23 | 新乡拓新药业股份有限公司 | 一种1,2,3‑三‑O‑乙酰基‑5‑脱氧‑β‑D‑核糖的制备方法 |
CN108484690A (zh) * | 2018-05-16 | 2018-09-04 | 新乡拓新药业股份有限公司 | 一种1,2,3-三-O-乙酰基-5-脱氧-β-D-核糖的制备方法 |
CN108727440A (zh) * | 2018-05-16 | 2018-11-02 | 新乡拓新药业股份有限公司 | 一种1,2,3-三-O-乙酰基-5-脱氧-β-D-核糖的制备方法 |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102260298B (zh) * | 2010-05-24 | 2014-04-09 | 重庆福安药业(集团)股份有限公司 | 一种合成1,2,3-O-三乙酰基-5-脱氧-β-D-核糖的方法 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100432088C (zh) * | 2007-01-30 | 2008-11-12 | 合肥巨林医药科技有限公司 | 1,2,3-三-o-乙酰基-5-脱氧-d-核糖合成方法 |
-
2007
- 2007-01-30 CN CNB2007100198737A patent/CN100432088C/zh not_active Expired - Fee Related
-
2008
- 2008-01-25 WO PCT/CN2008/070190 patent/WO2008092405A1/zh active Application Filing
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008092405A1 (fr) * | 2007-01-30 | 2008-08-07 | Donglin Tang | Procédé de synthèse du 1,2,3-tri-o-acétyl-5-désoxy-d-ribose |
WO2009044886A1 (ja) | 2007-10-05 | 2009-04-09 | Api Corporation | リボフラノース誘導体の製造方法 |
CN101993463A (zh) * | 2009-08-19 | 2011-03-30 | 成都康弘药业集团股份有限公司 | 一种卡培他滨及其中间体的制备方法 |
CN102432642A (zh) * | 2011-10-17 | 2012-05-02 | 江西科技师范学院 | 1, 2, 3-o-三乙酰基-5-脱氧-d-呋喃核糖的合成方法 |
CN103772450A (zh) * | 2012-10-18 | 2014-05-07 | 黑龙江福和华星制药集团股份有限公司 | 一种1,2,3-三乙酰基-5-脱氧-d-核糖的制法 |
CN103897005B (zh) * | 2012-12-27 | 2017-07-28 | 鲁南制药集团股份有限公司 | 一种连续操作合成卡培他滨的方法 |
CN104650160A (zh) * | 2015-01-13 | 2015-05-27 | 济南大学 | 卡培他滨关键中间体1,2,3-o-三乙酰基-5-脱氧-d-核糖的合成新方法 |
CN107118241A (zh) * | 2017-05-03 | 2017-09-01 | 南京信息工程大学 | 一种6‑硝基‑脱氧‑三乙酰基甲基葡萄糖苷的制备方法 |
CN107827938A (zh) * | 2017-10-27 | 2018-03-23 | 新乡拓新药业股份有限公司 | 一种1,2,3‑三‑O‑乙酰基‑5‑脱氧‑β‑D‑核糖的制备方法 |
CN107827938B (zh) * | 2017-10-27 | 2020-08-07 | 新乡拓新药业股份有限公司 | 一种1,2,3-三-O-乙酰基-5-脱氧-β-D-核糖的制备方法 |
CN108484690A (zh) * | 2018-05-16 | 2018-09-04 | 新乡拓新药业股份有限公司 | 一种1,2,3-三-O-乙酰基-5-脱氧-β-D-核糖的制备方法 |
CN108727440A (zh) * | 2018-05-16 | 2018-11-02 | 新乡拓新药业股份有限公司 | 一种1,2,3-三-O-乙酰基-5-脱氧-β-D-核糖的制备方法 |
CN108484690B (zh) * | 2018-05-16 | 2021-04-30 | 新乡拓新药业股份有限公司 | 一种1,2,3-三-O-乙酰基-5-脱氧-β-D-核糖的制备方法 |
Also Published As
Publication number | Publication date |
---|---|
CN100432088C (zh) | 2008-11-12 |
WO2008092405A1 (fr) | 2008-08-07 |
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Owner name: HEFEI KUI LIN MEDICAL CO., LTD. Free format text: FORMER OWNER: WANG CHENGJU; APPLICANT Effective date: 20080104 |
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Effective date of registration: 20080104 Address after: Baohe District of Hefei city of Anhui Province Wang Ping Tang Industrial Park Post encoding: 230051 Applicant after: Hefei Julin Pharmaceuticals, Inc. Address before: Zip code 208, 3 Hostel, eleven Middle Road, Fengyang Road, Yaohai District, Hefei, Anhui, China: 230001 Applicant before: Wang Cheng Ju Co-applicant before: Tang Donglin |
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