KR830004314A - syn-7-(2-아미노-4-티아졸릴)-(메톡시이미노)아세트아미도-3-아세톡시메틸-3-세펨-4-카복실산의 분리방법 - Google Patents
syn-7-(2-아미노-4-티아졸릴)-(메톡시이미노)아세트아미도-3-아세톡시메틸-3-세펨-4-카복실산의 분리방법 Download PDFInfo
- Publication number
- KR830004314A KR830004314A KR1019800003868A KR800003868A KR830004314A KR 830004314 A KR830004314 A KR 830004314A KR 1019800003868 A KR1019800003868 A KR 1019800003868A KR 800003868 A KR800003868 A KR 800003868A KR 830004314 A KR830004314 A KR 830004314A
- Authority
- KR
- South Korea
- Prior art keywords
- cepem
- methoxyimino
- acetoxymethyl
- acetamido
- thiazolyl
- Prior art date
Links
- 238000000926 separation method Methods 0.000 title 1
- -1 2-amino-4-thiazolyl Chemical group 0.000 claims 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 239000002244 precipitate Substances 0.000 claims 2
- 239000012453 solvate Substances 0.000 claims 2
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 claims 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims 1
- 229940126062 Compound A Drugs 0.000 claims 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims 1
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 125000002723 alicyclic group Chemical group 0.000 claims 1
- 239000012736 aqueous medium Substances 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
- C07D501/02—Preparation
- C07D501/12—Separation; Purification
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/542—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
- A61K31/545—Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
- C07D501/14—Compounds having a nitrogen atom directly attached in position 7
- C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
- C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
- C07D501/24—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
- C07D501/26—Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group
- C07D501/34—Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group with the 7-amino radical acylated by carboxylic acids containing hetero rings
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (2)
- syn-7-[2-(2-아미노-4-티아졸릴)-2-메톡시이미노]-아세트아미도-3-아세톡시메틸-3-세펨-4-카복실산과 알리사이클 에테르를 pH2.0 내지 3.5범위의 수용성 매질중에서 반응시켜 이 세펨산과 알리사이클에테르의 고형 용매화물을 제조하는 방법.
- (1) syn-7-[2-(2-아미노-4-티아졸릴)-2-메톡시이미노]-아세트아미도-3-아세톡시메틸-3-세펨-4-카복실산의 농도가 0.07몰/ℓ내지 0.4몰/ℓ인 수용성 반응 혼합물에 테트라하이드로푸란, 1,4-디옥산, 1,3-디옥소란 또는 테트라하이드로피란 같은 알리사이클에테르를 수용성 반응 혼합물의 0.1부피 내지 2부피를 첨가하고 또(2) 혼합물의 pH를 2.2내지 3.2로 조정한 후, 화합물 A의 용매화물 침전이 형성될 때까지 혼합물을 방치한후 침전물을 분리하는 단계 또는 이의 역순단계로 진행하는 것을 특징으로하는 수용성 반응 혼합물로부터 syn-7-[2-(2-아미노-4-티아졸릴)-2-메톡시이미노]-아세트아미도-3-아세톡시메틸-3-세펨-4-카복실산을 분리하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/082,822 US4252951A (en) | 1979-10-09 | 1979-10-09 | Isolation of syn-7-(2-amino-4-thiazolyl)-(methoxyimino)acetamido-3-acetoxymethyl-3-cephem-4-carboxylic acid |
US82822 | 1979-10-09 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR830004314A true KR830004314A (ko) | 1983-07-09 |
KR840000866B1 KR840000866B1 (ko) | 1984-06-20 |
Family
ID=22173679
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019800003868A KR840000866B1 (ko) | 1979-10-09 | 1980-10-08 | 세팔로스포린 용매화물의 제조방법 |
Country Status (27)
Country | Link |
---|---|
US (1) | US4252951A (ko) |
EP (1) | EP0027050B1 (ko) |
JP (1) | JPS5661388A (ko) |
KR (1) | KR840000866B1 (ko) |
AT (1) | AT369008B (ko) |
AU (1) | AU6306180A (ko) |
BE (1) | BE885569A (ko) |
CA (1) | CA1146539A (ko) |
CH (1) | CH647523A5 (ko) |
CS (1) | CS215142B2 (ko) |
DD (1) | DD153375A5 (ko) |
DE (1) | DE3065181D1 (ko) |
DK (1) | DK424680A (ko) |
ES (1) | ES495753A0 (ko) |
FI (1) | FI803200L (ko) |
FR (1) | FR2467211A1 (ko) |
GB (1) | GB2059966B (ko) |
GR (1) | GR70219B (ko) |
HU (1) | HU183230B (ko) |
IE (1) | IE50390B1 (ko) |
IL (1) | IL61227A (ko) |
IT (1) | IT1132926B (ko) |
PH (1) | PH15023A (ko) |
PT (1) | PT71886B (ko) |
RO (1) | RO80664B (ko) |
YU (1) | YU256480A (ko) |
ZA (1) | ZA806192B (ko) |
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DE60039132D1 (de) * | 1999-04-06 | 2008-07-17 | Sepracor Inc | O-Desmethylvenlafaxin-Succinat |
ATE504572T1 (de) * | 1999-09-02 | 2011-04-15 | Shionogi & Co | Derivate von aromatische heterocyclen enthaltende integraseinhibitoren |
CA2284459C (en) * | 1999-10-04 | 2012-12-11 | Neokimia Inc. | Combinatorial synthesis of libraries of macrocyclic compounds useful in drug discovery |
EP1246792B1 (en) * | 2000-01-13 | 2014-08-13 | Emisphere Technologies, Inc. | Compounds and compositions for delivering active agents |
ATE510547T1 (de) * | 2001-03-08 | 2011-06-15 | Univ Pennsylvania | Faciale amphiphile polymere als infektionsbekämpfende mittel |
NZ531139A (en) * | 2001-08-29 | 2007-09-28 | Neose Technologies Inc | Synthetic ganglioside derivatives and compositions thereof |
CA2498944C (en) * | 2002-09-19 | 2011-05-17 | Yasushi Kohno | Amino alcohol derivatives, salts thereof and immunosuppressive agents |
US7056916B2 (en) * | 2002-11-15 | 2006-06-06 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Medicaments for the treatment of chronic obstructive pulmonary disease |
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US7321065B2 (en) * | 2003-04-18 | 2008-01-22 | The Regents Of The University Of California | Thyronamine derivatives and analogs and methods of use thereof |
US20050203184A1 (en) | 2003-09-10 | 2005-09-15 | Petasis Nicos A. | Benzo lipoxin analogues |
CN1922133A (zh) * | 2004-01-23 | 2007-02-28 | 宾夕法尼亚州大学理事会 | 表面两亲性聚芳基和聚芳基炔基聚合物和低聚物及其用途 |
US7825278B2 (en) * | 2004-05-06 | 2010-11-02 | The Regents Of The University Of California | Substituted enaminones, their derivatives and uses thereof |
US20050255050A1 (en) * | 2004-05-14 | 2005-11-17 | Boehringer Ingelheim International Gmbh | Powder formulations for inhalation, comprising enantiomerically pure beta agonists |
US7220742B2 (en) * | 2004-05-14 | 2007-05-22 | Boehringer Ingelheim International Gmbh | Enantiomerically pure beta agonists, process for the manufacture thereof and use thereof as medicaments |
TWI403334B (zh) * | 2004-12-23 | 2013-08-01 | Merck Sharp & Dohme | 包含生物素殘基之抗血栓雙重抑制劑 |
JP2008531585A (ja) * | 2005-02-25 | 2008-08-14 | ザ・トラステイーズ・オブ・ザ・ユニバーシテイ・オブ・ペンシルベニア | 表面が両親媒性のポリマーおよびオリゴマー、それらの組成物そして癌治療方法におけるそれらの使用 |
CN101166706B (zh) * | 2005-02-28 | 2011-08-24 | 明治乳业株式会社 | 氢醌长链衍生物和/或苯氧基长链衍生物及含有它们的药品 |
AU2006279943B2 (en) * | 2005-08-10 | 2012-02-16 | The Johns Hopkins University | Polyamines useful as anti-parasitic and anti-cancer therapeutics and as lysine-specific demethylase inhibitors |
JP5270343B2 (ja) * | 2005-08-15 | 2013-08-21 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | ベータミメティックスの製造方法 |
US8592433B2 (en) * | 2005-10-28 | 2013-11-26 | Advait Nagle | Compounds and compositions as protein kinase inhibitors |
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ES2288107B1 (es) * | 2006-01-27 | 2008-11-01 | Fundacion Imabis Instituto Mediterraneo Para El Avance De La Biotecnologia Y La Investigacion Sanita | Derivados aciclicos saturados e insaturados de cadena larga de sulfamidas como activadores especificos de receptores ppar-alfa. |
FR2903004B1 (fr) * | 2006-07-03 | 2009-07-10 | Oreal | Utilisation en cosmetique d'un derive c-glycoside en association avec de l'acide ascorbique |
FR2902996B1 (fr) * | 2006-07-03 | 2008-09-26 | Oreal | Compositions cosmetiques associant un derive c-glycoside et un derive n-acylaminoamide |
US20090075935A1 (en) * | 2006-07-03 | 2009-03-19 | L'oreal | Composition comprising at least one c-glycoside derivative and at least one hyaluronic acid and its cosmetic use |
FR2902999B1 (fr) * | 2006-07-03 | 2012-09-28 | Oreal | Utilisation de derives c-glycoside a titre d'actif prodesquamant |
ES2375761T3 (es) * | 2006-12-14 | 2012-03-06 | Teva Pharmaceutical Industries Ltd. | Base de rasagilina cristalina sólida. |
CN101730706B (zh) * | 2007-05-11 | 2015-04-15 | 生物科技研究有限公司 | 具有神经保护和增强记忆活性的受体拮抗剂 |
US7696383B2 (en) * | 2007-06-26 | 2010-04-13 | Solvay Pharmaceuticals B.V. | N-oxides of venlafaxine and o-desmethylvenlafaxine as prodrugs |
FR2920000B1 (fr) * | 2007-08-13 | 2010-01-29 | Oreal | Composition cosmetique ou pharmaceutique contenant de l'acide hyaluronique, et procede cosmetique pour diminuer les signes du vieilissement |
US8252935B2 (en) * | 2007-10-19 | 2012-08-28 | Janssen Pharmaceutica N.V. | Piperidinyl and piperazinyl modulators of γ-secretase |
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US8063249B1 (en) * | 2008-04-25 | 2011-11-22 | Olema Pharmaceuticals, Inc. | Substituted triphenyl butenes |
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WO2010138828A2 (en) * | 2009-05-29 | 2010-12-02 | Abbott Laboratories | Potassium channel modulators |
US8288592B2 (en) * | 2009-09-22 | 2012-10-16 | Actavis Group Ptc Ehf | Solid state forms of tapentadol salts |
WO2012067824A1 (en) | 2010-11-16 | 2012-05-24 | Abbott Laboratories | Potassium channel modulators |
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Publication number | Priority date | Publication date | Assignee | Title |
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US3925372A (en) * | 1973-02-23 | 1975-12-09 | Lilly Co Eli | Alpha-aminoacyl-3-halo cephalosporins |
DK154939C (da) * | 1974-12-19 | 1989-06-12 | Takeda Chemical Industries Ltd | Analogifremgangsmaade til fremstilling af thiazolylacetamido-cephemforbindelser eller farmaceutisk acceptable salte eller estere deraf |
DE2760123C2 (de) * | 1976-01-23 | 1986-04-30 | Roussel-Uclaf, Paris | 7-Aminothiazolyl-syn-oxyiminoacetamidocephalosporansäuren, ihre Herstellung und sie enthaltende pharmazeutische Zusammensetzungen |
US4166115A (en) * | 1976-04-12 | 1979-08-28 | Fujisawa Pharmaceutical Co., Ltd. | Syn 7-oxoimino substituted derivatives of cephalosporanic acid |
-
1979
- 1979-10-09 US US06/082,822 patent/US4252951A/en not_active Expired - Lifetime
-
1980
- 1980-10-07 DE DE8080303525T patent/DE3065181D1/de not_active Expired
- 1980-10-07 YU YU02564/80A patent/YU256480A/xx unknown
- 1980-10-07 JP JP14111980A patent/JPS5661388A/ja active Pending
- 1980-10-07 IL IL61227A patent/IL61227A/xx unknown
- 1980-10-07 PH PH24677A patent/PH15023A/en unknown
- 1980-10-07 GR GR63068A patent/GR70219B/el unknown
- 1980-10-07 CS CS806756A patent/CS215142B2/cs unknown
- 1980-10-07 CA CA000361704A patent/CA1146539A/en not_active Expired
- 1980-10-07 GB GB8032258A patent/GB2059966B/en not_active Expired
- 1980-10-07 FR FR8021431A patent/FR2467211A1/fr active Granted
- 1980-10-07 ZA ZA00806192A patent/ZA806192B/xx unknown
- 1980-10-07 AT AT0498080A patent/AT369008B/de not_active IP Right Cessation
- 1980-10-07 PT PT71886A patent/PT71886B/pt unknown
- 1980-10-07 EP EP80303525A patent/EP0027050B1/en not_active Expired
- 1980-10-08 DD DD80224408A patent/DD153375A5/de unknown
- 1980-10-08 ES ES495753A patent/ES495753A0/es active Granted
- 1980-10-08 RO RO102315A patent/RO80664B/ro unknown
- 1980-10-08 DK DK424680A patent/DK424680A/da not_active Application Discontinuation
- 1980-10-08 CH CH7518/80A patent/CH647523A5/fr not_active IP Right Cessation
- 1980-10-08 AU AU63061/80A patent/AU6306180A/en not_active Abandoned
- 1980-10-08 HU HU802455A patent/HU183230B/hu unknown
- 1980-10-08 KR KR1019800003868A patent/KR840000866B1/ko active
- 1980-10-08 BE BE1/9975A patent/BE885569A/fr not_active IP Right Cessation
- 1980-10-08 IT IT25200/80A patent/IT1132926B/it active
- 1980-10-08 IE IE2086/80A patent/IE50390B1/en unknown
- 1980-10-09 FI FI803200A patent/FI803200L/fi not_active Application Discontinuation
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GB1295696A (ko) | ||
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