SU583763A3 - Способ получени адриамицинов - Google Patents
Способ получени адриамициновInfo
- Publication number
- SU583763A3 SU583763A3 SU7502115054A SU2115054A SU583763A3 SU 583763 A3 SU583763 A3 SU 583763A3 SU 7502115054 A SU7502115054 A SU 7502115054A SU 2115054 A SU2115054 A SU 2115054A SU 583763 A3 SU583763 A3 SU 583763A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- formula
- solution
- general formula
- group
- mixture
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 5
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 18
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 10
- UKWHYYKOEPRTIC-UHFFFAOYSA-N mercury(ii) oxide Chemical compound [Hg]=O UKWHYYKOEPRTIC-UHFFFAOYSA-N 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- NGYIMTKLQULBOO-UHFFFAOYSA-L mercury dibromide Chemical compound Br[Hg]Br NGYIMTKLQULBOO-UHFFFAOYSA-L 0.000 claims description 4
- 229940101209 mercuric oxide Drugs 0.000 claims description 3
- 230000015572 biosynthetic process Effects 0.000 claims description 2
- 238000001704 evaporation Methods 0.000 claims description 2
- 230000008020 evaporation Effects 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 239000003153 chemical reaction reagent Substances 0.000 claims 1
- 230000003993 interaction Effects 0.000 claims 1
- 125000006239 protecting group Chemical group 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 18
- 239000000243 solution Substances 0.000 description 15
- AOJJSUZBOXZQNB-TZSSRYMLSA-N Doxorubicin Chemical class O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-TZSSRYMLSA-N 0.000 description 7
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 150000002402 hexoses Chemical class 0.000 description 4
- 229910052938 sodium sulfate Inorganic materials 0.000 description 4
- 235000011152 sodium sulphate Nutrition 0.000 description 4
- IBZGBXXTIGCACK-CWKPULSASA-N Adriamycinone Chemical class C1[C@@](O)(C(=O)CO)C[C@H](O)C2=C1C(O)=C1C(=O)C(C=CC=C3OC)=C3C(=O)C1=C2O IBZGBXXTIGCACK-CWKPULSASA-N 0.000 description 3
- 229940009456 adriamycin Drugs 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000002808 molecular sieve Substances 0.000 description 3
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- YOFDHOWPGULAQF-MQJDWESPSA-N (7s,9s)-9-acetyl-6,7,9,11-tetrahydroxy-4-methoxy-8,10-dihydro-7h-tetracene-5,12-dione Chemical compound C1[C@@](O)(C(C)=O)C[C@H](O)C2=C1C(O)=C1C(=O)C(C=CC=C3OC)=C3C(=O)C1=C2O YOFDHOWPGULAQF-MQJDWESPSA-N 0.000 description 1
- HEWZVZIVELJPQZ-UHFFFAOYSA-N 2,2-dimethoxypropane Chemical compound COC(C)(C)OC HEWZVZIVELJPQZ-UHFFFAOYSA-N 0.000 description 1
- YOFDHOWPGULAQF-UHFFFAOYSA-N Daunomycin-Aglycone Natural products C1C(O)(C(C)=O)CC(O)C2=C1C(O)=C1C(=O)C(C=CC=C3OC)=C3C(=O)C1=C2O YOFDHOWPGULAQF-UHFFFAOYSA-N 0.000 description 1
- 229910005831 GeO3 Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- OAIVIYSBZFEOIU-UHFFFAOYSA-N chloroform;propan-2-one Chemical compound CC(C)=O.ClC(Cl)Cl OAIVIYSBZFEOIU-UHFFFAOYSA-N 0.000 description 1
- 229960001904 epirubicin Drugs 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000000725 suspension Substances 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
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/20—Carbocyclic rings
- C07H15/24—Condensed ring systems having three or more rings
- C07H15/252—Naphthacene radicals, e.g. daunomycins, adriamycins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biotechnology (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1278374A GB1457632A (en) | 1974-03-22 | 1974-03-22 | Adriamycins |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU583763A3 true SU583763A3 (ru) | 1977-12-05 |
Family
ID=10011048
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU7502115054A SU583763A3 (ru) | 1974-03-22 | 1975-03-21 | Способ получени адриамицинов |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US4058519A (enExample) |
| JP (1) | JPS5840555B2 (enExample) |
| AT (1) | AT338420B (enExample) |
| AU (1) | AU497500B2 (enExample) |
| BE (1) | BE826978A (enExample) |
| CA (1) | CA1046507A (enExample) |
| CH (1) | CH612947A5 (enExample) |
| DE (1) | DE2510866C3 (enExample) |
| DK (1) | DK153158C (enExample) |
| ES (1) | ES435833A1 (enExample) |
| FR (1) | FR2264555B1 (enExample) |
| GB (1) | GB1457632A (enExample) |
| HK (1) | HK882A (enExample) |
| MY (1) | MY103912A (enExample) |
| NL (1) | NL176635C (enExample) |
| SE (1) | SE434844B (enExample) |
| SU (1) | SU583763A3 (enExample) |
| ZA (1) | ZA751781B (enExample) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4133877A (en) * | 1976-07-08 | 1979-01-09 | Societa Farmaceutici Italia S.P.A. | Anthracycline ethers and use therefor |
| US4201773A (en) * | 1978-07-26 | 1980-05-06 | The United States Of America As Represented By The Department Of Health, Education And Welfare | 7-O-(2,6-Dideoxy-α-L-lyxo-hexopyranosyl)-daunomycinone, desmethoxy daunomycinone, adriamycinone, and carminomycinone |
| US4345068A (en) * | 1979-11-22 | 1982-08-17 | Farmitalia Carlo Erba S.P.A. | Process for the preparation of 4'-epidaunorubicin, 3',4'-diepidaunorubicin, their doxorubicin analogs, and intermediates used in said process |
| JPS57106694A (en) * | 1980-11-01 | 1982-07-02 | Erba Carlo Spa | Anthracycline glycoside |
| JPS57106695A (en) * | 1980-11-01 | 1982-07-02 | Erba Carlo Spa | Anthracycline g lycoside compound |
| US4562177A (en) * | 1982-08-17 | 1985-12-31 | The Ohio State University Research Foundation | 3'-Amino-2' halo-anthracycline antibiotics |
| US4537882A (en) * | 1984-05-10 | 1985-08-27 | Ohio State University | 4-Demethoxy-3'-desamino-2'-halo-anthracycline and pharmaceutical composition containing same |
| DE3500029A1 (de) * | 1985-01-02 | 1986-09-04 | Farmitalia Carlo Erba S.p.A., Mailand/Milano | Anthracyclinester |
| GB2169284A (en) * | 1985-01-05 | 1986-07-09 | Erba Farmitalia | 4'-Epidoxorubicin-14-esters |
| JPS61172891A (ja) * | 1985-01-24 | 1986-08-04 | フア−ミタリア・カルロ・エルバ・ソシエタ・ペル・アツイオ−ニ | アントラサイクリン類エステルの製法 |
| US5124318A (en) * | 1985-08-02 | 1992-06-23 | Farmitalia Carlo Erba S.R.L. | Injectable ready-to-use solutions containing an antitumor anthracycline glycoside |
| US5124317A (en) * | 1985-08-02 | 1992-06-23 | Farmitalia Carlo Erba S.P.A. | Injectable ready-to-use solutions containing an antitumor anthracycline glycoside |
| US5977082A (en) * | 1985-08-02 | 1999-11-02 | Pharmacia & Upjohn Company | Injectable ready-to-use solutions containing an antitumor anthracycline glycoside |
| GB8519452D0 (en) * | 1985-08-02 | 1985-09-11 | Erba Farmitalia | Injectable solutions |
| ATE195526T1 (de) | 1996-12-16 | 2000-09-15 | Pharmachemie Bv | Verfahren zur herstellung von epirubicin oder zusatzsalzen davon, von daunorubicin |
| DE69922681T2 (de) * | 1998-10-16 | 2005-05-25 | Mercian Corp. | Kristallisation von doxorubicin-hydrochlorid |
| KR100850408B1 (ko) * | 2000-08-10 | 2008-08-04 | 동아제약주식회사 | 안트라싸이클린계 항암제인 에피루비신 및 약학적으로허용되는 그 염의 제조방법 |
| KR100785966B1 (ko) * | 2000-08-10 | 2007-12-14 | 동아제약주식회사 | 안트라싸이클린계 항암제인 에피루비신 및 약학적으로허용되는 그 염의 제조방법 |
| DE04777189T1 (de) * | 2003-07-02 | 2011-04-07 | Solux Corporation, San Diego | Thermisch stabiles kristallines epirubicin-hydrochlorid und herstellungsverfahren dafür |
| KR101345002B1 (ko) | 2005-01-21 | 2013-12-31 | 아스텍스 테라퓨틱스 리미티드 | 제약 화합물 |
| PL375008A1 (pl) | 2005-05-12 | 2006-11-13 | Institut National De La Sante Et De La Recherche Medicale, Inserm | Nowe zastosowanie medyczne chlorowodorku epirubicyny |
| EP2073807A1 (en) | 2006-10-12 | 2009-07-01 | Astex Therapeutics Limited | Pharmaceutical combinations |
| JP5528806B2 (ja) | 2006-10-12 | 2014-06-25 | アステックス、セラピューティックス、リミテッド | 複合薬剤 |
| US8173621B2 (en) | 2008-06-11 | 2012-05-08 | Gilead Pharmasset Llc | Nucleoside cyclicphosphates |
| NZ593647A (en) | 2008-12-23 | 2013-08-30 | Gilead Pharmasset Llc | Synthesis of purine nucleosides |
| US8551973B2 (en) | 2008-12-23 | 2013-10-08 | Gilead Pharmasset Llc | Nucleoside analogs |
| SG172359A1 (en) | 2008-12-23 | 2011-07-28 | Pharmasset Inc | Nucleoside phosphoramidates |
| JP2013527145A (ja) | 2010-03-31 | 2013-06-27 | ギリード・ファーマセット・エルエルシー | リン含有活性化剤の立体選択的合成 |
| WO2017120729A1 (zh) * | 2016-01-11 | 2017-07-20 | 浙江海正药业股份有限公司 | 一种盐酸表柔比星的制备方法及其中间体 |
| SG11201807965YA (en) | 2016-03-15 | 2018-10-30 | Oryzon Genomics Sa | Combinations of lsd1 inhibitors for use in the treatment of solid tumors |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3356674A (en) * | 1961-07-07 | 1967-12-05 | Rikagaku Kenkyusho | 3-c-hydroxymethyl-3, 5-didesoxy-l-lyxofuranose and its derivatives, and a process for the production thereof |
| US3427300A (en) * | 1965-11-12 | 1969-02-11 | Merck & Co Inc | Anti-inflammatory steroid 2'-acetamido-2'-deoxy-glucoside compounds |
| YU33730B (en) * | 1967-04-18 | 1978-02-28 | Farmaceutici Italia | Process for preparing a novel antibiotic substance and salts thereof |
| US3803124A (en) * | 1968-04-12 | 1974-04-09 | Farmaceutici It Soc | Process for the preparation of adriamycin and adriamycinone and adriamycin derivatives |
| US3629231A (en) * | 1968-05-23 | 1971-12-21 | Biorex Laboratories Ltd | Derivatives of glycyrrhetinic acid |
| US3651090A (en) * | 1969-12-17 | 1972-03-21 | Cutter Lab | 1 3-dioxolan-4-yl-alkyl guanidines |
| FR2183710A1 (en) * | 1972-05-06 | 1973-12-21 | Farmaceutici Italia | Daunomycin (hydrochloride) prepn - by reaction of daunomycinone with daunosamines, useful as antitumour agent and anti-leucemic |
-
1974
- 1974-03-22 GB GB1278374A patent/GB1457632A/en not_active Expired
-
1975
- 1975-03-12 NL NLAANVRAGE7502934,A patent/NL176635C/xx not_active IP Right Cessation
- 1975-03-13 DE DE2510866A patent/DE2510866C3/de not_active Expired
- 1975-03-18 AT AT207475A patent/AT338420B/de not_active IP Right Cessation
- 1975-03-19 AU AU79263/75A patent/AU497500B2/en not_active Expired
- 1975-03-19 FR FR7508548A patent/FR2264555B1/fr not_active Expired
- 1975-03-19 US US05/560,104 patent/US4058519A/en not_active Expired - Lifetime
- 1975-03-20 ZA ZA00751781A patent/ZA751781B/xx unknown
- 1975-03-20 DK DK114475A patent/DK153158C/da not_active IP Right Cessation
- 1975-03-20 JP JP50033095A patent/JPS5840555B2/ja not_active Expired
- 1975-03-20 CA CA222,609A patent/CA1046507A/en not_active Expired
- 1975-03-20 SE SE7503215A patent/SE434844B/xx active Protection Beyond IP Right Term
- 1975-03-21 SU SU7502115054A patent/SU583763A3/ru active
- 1975-03-21 BE BE154581A patent/BE826978A/xx not_active IP Right Cessation
- 1975-03-21 CH CH365975A patent/CH612947A5/xx not_active IP Right Cessation
- 1975-03-21 ES ES435833A patent/ES435833A1/es not_active Expired
-
1982
- 1982-01-14 HK HK8/82A patent/HK882A/xx unknown
-
1988
- 1988-09-14 MY MYPI88001026A patent/MY103912A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ES435833A1 (es) | 1976-12-01 |
| MY103912A (en) | 1993-10-30 |
| US4058519A (en) | 1977-11-15 |
| FR2264555A1 (enExample) | 1975-10-17 |
| DK153158C (da) | 1989-01-16 |
| DE2510866A1 (de) | 1975-10-02 |
| JPS5840555B2 (ja) | 1983-09-06 |
| HK882A (en) | 1982-01-22 |
| CH612947A5 (enExample) | 1979-08-31 |
| ZA751781B (en) | 1976-02-25 |
| JPS50126656A (enExample) | 1975-10-04 |
| SE434844B (sv) | 1984-08-20 |
| AT338420B (de) | 1977-08-25 |
| ATA207475A (de) | 1976-12-15 |
| NL176635C (nl) | 1985-05-17 |
| NL7502934A (nl) | 1975-09-24 |
| SE7503215L (enExample) | 1975-09-23 |
| GB1457632A (en) | 1976-12-08 |
| DK153158B (da) | 1988-06-20 |
| DE2510866C3 (de) | 1980-08-14 |
| DK114475A (enExample) | 1975-09-23 |
| FR2264555B1 (enExample) | 1980-01-11 |
| CA1046507A (en) | 1979-01-16 |
| NL176635B (nl) | 1984-12-17 |
| AU7926375A (en) | 1976-09-23 |
| BE826978A (fr) | 1975-09-22 |
| AU497500B2 (en) | 1978-12-14 |
| DE2510866B2 (de) | 1979-12-06 |
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