CN1415615A - New compound of natrium cefdinir - Google Patents

New compound of natrium cefdinir Download PDF

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Publication number
CN1415615A
CN1415615A CN 02146335 CN02146335A CN1415615A CN 1415615 A CN1415615 A CN 1415615A CN 02146335 CN02146335 CN 02146335 CN 02146335 A CN02146335 A CN 02146335A CN 1415615 A CN1415615 A CN 1415615A
Authority
CN
China
Prior art keywords
cefdinir
new compound
natrium
sodium
mol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN 02146335
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Chinese (zh)
Inventor
王登之
侯朋
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CN 02146335 priority Critical patent/CN1415615A/en
Publication of CN1415615A publication Critical patent/CN1415615A/en
Pending legal-status Critical Current

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  • Cephalosporin Compounds (AREA)

Abstract

A novel compound, cephalosporin Toubaodinina, for treating the infection caused by sensitive bacteria, or child infection is prepared through the reaction of Toubaodini on sodium dicarbonate, deposition in alcohol, filter, and low-temp vacuum drying. Its advantages are high water solubility and easy absorption for oral application.

Description

New compound Cefdinir sodium
Technical field
The present invention relates to nitrogenous and heterogeneous ring compound sulphur; particularly relate to Cefdinir sodium (title is [6R-[6 α, 7 β (Z)]]-7-[[(2-amino-4-thiazolyl)-(oximido) ethanoyl] amino]-3-vinyl-8-oxygen-5-thia-1-azabicyclic [4.2.0] oct-2-ene-2-carboxylic acid sodium).
Background technology
Because Cefdinir is water insoluble, as antibiotic medicine, oral post-absorption is bad, therefore, changes the water-soluble of Cefdinir, become now urgent problem it
Summary of the invention
The objective of the invention is to overcome above-mentioned the deficiencies in the prior art part, and provide a kind of synthetic convenience, the new Cefdinir sodium of good water solubility.
The object of the invention can reach by following measure: it is at normal temperatures and pressures, carry out complete reaction by 1 mol Cefdinir and 1 mol sodium bicarbonate after, add ethanol sedimentation, suction filtration, low-temperature vacuum drying promptly obtains this patent product Cefdinir sodium.
Reaction formula is:
Character:
Fusing point: not clear, 160 ℃ of left and right sides flavescence slowly increase the weight of to be brown afterwards, and 190 ℃ of left and right sides blackening and decomposing are yellow crystalline powder, and odorless or slightly special smell are soluble in water.
Product of the present invention has following advantage compared to existing technology: because this product is synthetic uncomplicated, be antibiotic medicine, soluble in water, oral absorption is good, has improved drug effect.
Embodiment
Embodiment 1
At normal temperatures and pressures, 1 mol Cefdinir and 1 mol sodium bicarbonate are put into reaction flask constantly stir, after reacting completely, in bottle, add ethanol sedimentation, suction filtration, low-temperature vacuum drying promptly obtains this patent product Cefdinir sodium.
Purposes:
Cefdinir is a third generation cephalosporin, indication be due to the various sensitive strains in, severe infection, also can be used for paediatrics and infect.
Compare with s-generation cephalo, the third generation cephalosporin antimicrobial spectrum is wider, anti-microbial activity is stronger, more stable to bacteriogenic β-Nei Xiananmei, especially more stable to the I fermentoid, therefore have stronger sterilizing ability to producing I zymoid negative bacillus such as enterobacteria, Serratia and Pseudomonas aeruginosa, its super broad-spectrum antibacterial action has covered most Gram-negatives and positive bacteria, particularly to the gram-positive microorganism effect than two generation cynnematin obviously strengthen.

Claims (1)

1, a kind of new compound Cefdinir sodium, its feature at normal temperatures and pressures, carry out complete reaction by 1 mol Cefdinir and 1 mol sodium bicarbonate after, add ethanol sedimentation, suction filtration, low-temperature vacuum drying promptly obtains this patent product.
CN 02146335 2002-10-24 2002-10-24 New compound of natrium cefdinir Pending CN1415615A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 02146335 CN1415615A (en) 2002-10-24 2002-10-24 New compound of natrium cefdinir

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 02146335 CN1415615A (en) 2002-10-24 2002-10-24 New compound of natrium cefdinir

Publications (1)

Publication Number Publication Date
CN1415615A true CN1415615A (en) 2003-05-07

Family

ID=4751052

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 02146335 Pending CN1415615A (en) 2002-10-24 2002-10-24 New compound of natrium cefdinir

Country Status (1)

Country Link
CN (1) CN1415615A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100381445C (en) * 2003-11-05 2008-04-16 余安国 Cefetamet sodium and its application of preparing powder injection or dry powder injection for broad-spectrum strong antibiotic injection
WO2010075765A1 (en) 2008-12-31 2010-07-08 浙江奥默生物医药有限公司 Cefdinir acid double salt and its preparation

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100381445C (en) * 2003-11-05 2008-04-16 余安国 Cefetamet sodium and its application of preparing powder injection or dry powder injection for broad-spectrum strong antibiotic injection
WO2010075765A1 (en) 2008-12-31 2010-07-08 浙江奥默生物医药有限公司 Cefdinir acid double salt and its preparation
CN101481383B (en) * 2008-12-31 2012-01-11 杭州奥默医药技术有限公司 Cefdinir acid type double salt compound and preparation
RU2531276C2 (en) * 2008-12-31 2014-10-20 Чжецзян Адамерк Биофармлабс Инк. Cefdinir acid salt and method of obtaining thereof

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C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication