DE2036906A1 - Cephalosponnverbmdungen - Google Patents
CephalosponnverbmdungenInfo
- Publication number
- DE2036906A1 DE2036906A1 DE19702036906 DE2036906A DE2036906A1 DE 2036906 A1 DE2036906 A1 DE 2036906A1 DE 19702036906 DE19702036906 DE 19702036906 DE 2036906 A DE2036906 A DE 2036906A DE 2036906 A1 DE2036906 A1 DE 2036906A1
- Authority
- DE
- Germany
- Prior art keywords
- cephalexin
- methanol
- crystal form
- water
- vwd
- 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
Links
- 150000001875 compounds Chemical class 0.000 title 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 66
- ZAIPMKNFIOOWCQ-UEKVPHQBSA-N cephalexin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@@H]3N(C2=O)C(=C(CS3)C)C(O)=O)=CC=CC=C1 ZAIPMKNFIOOWCQ-UEKVPHQBSA-N 0.000 claims description 31
- 229940106164 cephalexin Drugs 0.000 claims description 31
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 13
- 239000013078 crystal Substances 0.000 claims description 10
- 239000000725 suspension Substances 0.000 claims description 7
- 239000012535 impurity Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 238000010586 diagram Methods 0.000 claims description 3
- 238000001035 drying Methods 0.000 claims description 2
- 238000001914 filtration Methods 0.000 claims description 2
- 238000005406 washing Methods 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 238000002329 infrared spectrum Methods 0.000 description 7
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 239000007858 starting material Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 239000002002 slurry Substances 0.000 description 4
- 238000001228 spectrum Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 229930186147 Cephalosporin Natural products 0.000 description 3
- 239000012736 aqueous medium Substances 0.000 description 3
- 229940124587 cephalosporin Drugs 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- -1 Cephalosporin compounds Chemical class 0.000 description 2
- QHTOIDKCEPKVCM-ZCFIWIBFSA-N cepham Chemical compound S1CCCN2C(=O)C[C@H]21 QHTOIDKCEPKVCM-ZCFIWIBFSA-N 0.000 description 2
- 238000001962 electrophoresis Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N formic acid Substances OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 229940046892 lead acetate Drugs 0.000 description 2
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 229930193140 Neomycin Natural products 0.000 description 1
- 229930182555 Penicillin Natural products 0.000 description 1
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 1
- 238000004279 X-ray Guinier Methods 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 150000001780 cephalosporins Chemical class 0.000 description 1
- 150000001782 cephems Chemical class 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 230000029052 metamorphosis Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229960004927 neomycin Drugs 0.000 description 1
- 229940049954 penicillin Drugs 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 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
- C07D501/14—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
- C07D501/22—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with radicals containing only hydrogen and carbon atoms, attached in position 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/12—Radicals substituted by oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Cephalosporin Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3749169 | 1969-07-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2036906A1 true DE2036906A1 (de) | 1971-02-04 |
Family
ID=10396869
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19702036906 Pending DE2036906A1 (de) | 1969-07-25 | 1970-07-24 | Cephalosponnverbmdungen |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3728341A (forum.php) |
| BE (1) | BE753910A (forum.php) |
| CA (1) | CA958010A (forum.php) |
| DE (1) | DE2036906A1 (forum.php) |
| FR (1) | FR2055598A5 (forum.php) |
| GB (1) | GB1315484A (forum.php) |
| ZA (1) | ZA705121B (forum.php) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005147399A (ja) * | 2003-11-13 | 2005-06-09 | Staeubli Faverges | 雌継手要素とそのような要素を組込む迅速継手 |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1001615A (en) * | 1971-12-04 | 1976-12-14 | Takeda Chemical Industries Ltd. | Method for purification of cephalexin |
| US3862186A (en) * | 1972-12-15 | 1975-01-21 | Bristol Myers Co | Process for the production of cephalexin monohydrate |
-
1969
- 1969-07-25 GB GB3749169A patent/GB1315484A/en not_active Expired
-
1970
- 1970-07-20 US US00056261A patent/US3728341A/en not_active Expired - Lifetime
- 1970-07-24 DE DE19702036906 patent/DE2036906A1/de active Pending
- 1970-07-24 CA CA089,083A patent/CA958010A/en not_active Expired
- 1970-07-24 ZA ZA705121A patent/ZA705121B/xx unknown
- 1970-07-24 BE BE753910D patent/BE753910A/xx unknown
- 1970-07-24 FR FR7027422A patent/FR2055598A5/fr not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005147399A (ja) * | 2003-11-13 | 2005-06-09 | Staeubli Faverges | 雌継手要素とそのような要素を組込む迅速継手 |
Also Published As
| Publication number | Publication date |
|---|---|
| BE753910A (forum.php) | 1971-01-25 |
| CA958010A (en) | 1974-11-19 |
| FR2055598A5 (forum.php) | 1971-05-07 |
| US3728341A (en) | 1973-04-17 |
| ZA705121B (en) | 1972-02-23 |
| GB1315484A (en) | 1973-05-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2505304C2 (de) | Verfahren zur Herstellung von Calciumcarbonat | |
| EP0133444B1 (de) | Verfahren zur Herstellung von als schattengebende Komponente in Röntgenkontrastmitteln geeignetes Bariumsulfat mit erhöhter Fliessfähigkeit und Dichte, nach diesem Verfahren erhaltenes Produkt und daraus hergestellte Röntgenkontrastmittel | |
| DE2317352C2 (de) | Perlförmige Zusammensetzung und Verfahren zu ihrer Herstellung | |
| DE2901730C2 (forum.php) | ||
| DE1244146B (de) | Verfahren zum reinigen von wasserloeslichen hydroxyalkylaethern von galactomannanen | |
| DE2557287A1 (de) | Verfahren zur reinigung von roher chenodesoxycholsaeure | |
| DE2721027A1 (de) | Verfahren zur reinigung von glucagon | |
| DE2322928A1 (de) | Dispergierzubereitungen auf ligninbasis und verfahren zu ihrer herstellung | |
| DE2618146C3 (de) | Verfahren zur Extraktion einer süßen Substanz, wäßriger Extrakt, enthaltend eine süße Substanz bzw. entsprechender gefriergetrockneter Extrakt | |
| DE1244145B (de) | Verfahren zum Reinigen von wasserloeslicher Hydroxyaethylcellulose | |
| DE2361169B2 (de) | Verfahren zur aktivierung von von detengensspuren befreiter cholesterinoxydase | |
| DE2036906A1 (de) | Cephalosponnverbmdungen | |
| EP1756132A1 (de) | Verfahren zur herstellung von eisensaccharosekomplex | |
| DE2535311A1 (de) | Verfahren zur herstellung von celluloseaethern mit verbesserter dispergierbarkeit in waessrigen fluessigkeiten und nach dem verfahren hergestellte celluloseaether | |
| DE2700011C2 (forum.php) | ||
| DE945407C (de) | Verfahren zur Gewinnung und Reindarstellung von Bacitracin | |
| AT325580B (de) | Verfahren zur herstellung von zur klärung und stabilisierung von getränken, insbesondere von weinen, geeigneten bentoniten | |
| DE1622294C3 (forum.php) | ||
| DE1642592C (de) | Verfahren zur Gewinnung von praktisch Fremdoxydase freier Glucose oxydase | |
| DE1617948C (de) | Verfahren zur Herstellung eines das retikuloendothelialen Systems stimulieren den Stoffs | |
| DE933450C (de) | Verfahren zur Herstellung eines neuen Salzes von Penicillin G | |
| DE852084C (de) | Verfahren zur Herstellung von sekundaeren Celluloseestern | |
| DE1806625A1 (de) | Verfahren zur Herstellung von Chymotrypsin B | |
| DE2208631C3 (de) | N-Isobornyloxycarbonylcephalosporin C, Verfahren zu seiner Herstellung und Verwendung zur Herstellung von Cephalosporin C | |
| AT123849B (de) | Verfahren zur Darstellung von Celluloseformiaten. |