FI60703C - Friflytande kristaller av foereningarnas pge2 och pgf2 alfa salter anvaendbara foer foedelsekontroll i daeggdjur - Google Patents
Friflytande kristaller av foereningarnas pge2 och pgf2 alfa salter anvaendbara foer foedelsekontroll i daeggdjur Download PDFInfo
- Publication number
- FI60703C FI60703C FI770520A FI770520A FI60703C FI 60703 C FI60703 C FI 60703C FI 770520 A FI770520 A FI 770520A FI 770520 A FI770520 A FI 770520A FI 60703 C FI60703 C FI 60703C
- Authority
- FI
- Finland
- Prior art keywords
- pge2
- acetonitrile
- crystals
- solution
- salt
- Prior art date
Links
- XEYBRNLFEZDVAW-ARSRFYASSA-N dinoprostone Chemical compound CCCCC[C@H](O)\C=C\[C@H]1[C@H](O)CC(=O)[C@@H]1C\C=C/CCCC(O)=O XEYBRNLFEZDVAW-ARSRFYASSA-N 0.000 title description 17
- 229960002986 dinoprostone Drugs 0.000 title description 16
- XEYBRNLFEZDVAW-UHFFFAOYSA-N prostaglandin E2 Natural products CCCCCC(O)C=CC1C(O)CC(=O)C1CC=CCCCC(O)=O XEYBRNLFEZDVAW-UHFFFAOYSA-N 0.000 title description 16
- PXGPLTODNUVGFL-BRIYLRKRSA-N (E,Z)-(1R,2R,3R,5S)-7-(3,5-Dihydroxy-2-((3S)-(3-hydroxy-1-octenyl))cyclopentyl)-5-heptenoic acid Chemical compound CCCCC[C@H](O)C=C[C@H]1[C@H](O)C[C@H](O)[C@@H]1CC=CCCCC(O)=O PXGPLTODNUVGFL-BRIYLRKRSA-N 0.000 title description 11
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 90
- 239000013078 crystal Substances 0.000 description 28
- 239000000243 solution Substances 0.000 description 28
- 150000003839 salts Chemical class 0.000 description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 20
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical class OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 19
- 239000000203 mixture Substances 0.000 description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- 238000003756 stirring Methods 0.000 description 8
- 150000001412 amines Chemical class 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 150000003180 prostaglandins Chemical class 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 239000011521 glass Substances 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000002425 crystallisation Methods 0.000 description 4
- 230000008025 crystallization Effects 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000010253 intravenous injection Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 235000019439 ethyl acetate Nutrition 0.000 description 2
- 239000012065 filter cake Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- 230000000144 pharmacologic effect Effects 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000000712 assembly Effects 0.000 description 1
- 238000000429 assembly Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- -1 butyl nitrile Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000002024 ethyl acetate extract Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical class CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US4245870A | 1970-06-01 | 1970-06-01 | |
| US4245870 | 1970-06-01 | ||
| FI1499/71A FI53308C (fi) | 1970-06-01 | 1971-05-28 | Foerfarande foer framstaellning av dammfria kristaller av foereningarnas pge2 och pgf2a tris (hydroxymetyl) aminometansalter med farmakologisk och medicinsk anvaendning |
| FI149971 | 1971-05-28 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI770520A7 FI770520A7 (enrdf_load_stackoverflow) | 1977-02-17 |
| FI60703B FI60703B (fi) | 1981-11-30 |
| FI60703C true FI60703C (fi) | 1982-03-10 |
Family
ID=26156482
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI770520A FI60703C (fi) | 1970-06-01 | 1977-02-17 | Friflytande kristaller av foereningarnas pge2 och pgf2 alfa salter anvaendbara foer foedelsekontroll i daeggdjur |
| FI770521A FI770521A7 (enrdf_load_stackoverflow) | 1970-06-01 | 1977-02-17 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI770521A FI770521A7 (enrdf_load_stackoverflow) | 1970-06-01 | 1977-02-17 |
Country Status (1)
| Country | Link |
|---|---|
| FI (2) | FI60703C (enrdf_load_stackoverflow) |
-
1977
- 1977-02-17 FI FI770520A patent/FI60703C/fi not_active IP Right Cessation
- 1977-02-17 FI FI770521A patent/FI770521A7/fi not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| FI770520A7 (enrdf_load_stackoverflow) | 1977-02-17 |
| FI770521A7 (enrdf_load_stackoverflow) | 1977-02-17 |
| FI60703B (fi) | 1981-11-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH04253941A (ja) | イブプロフェンリシネートの生成及び分割 | |
| CA1228851A (en) | Crystalline ceftazidime salts | |
| JPS5885893A (ja) | ７−β−〔２−（２−アミノチアゾ−ル−４−イル）−２−シン−メトキシイミノアセトアミド〕−３−（５−カルボキシメチル−４−メチル−１，３−チアゾ−ル−２−イルチオメチル）セフ−３−エム−４−カルボン酸の結晶質水溶性塩およびその製造方法 | |
| US3657327A (en) | Prostaglandin salts of tris(hydroxymethyl)aminomethane | |
| FI60703C (fi) | Friflytande kristaller av foereningarnas pge2 och pgf2 alfa salter anvaendbara foer foedelsekontroll i daeggdjur | |
| KR100532898B1 (ko) | 플루다라빈 포스페이트의 제조를 위한 정제 방법 | |
| US4294766A (en) | Preparation of pure potassium ribonate and ribonolactone | |
| JPS5810561A (ja) | Ｐｇｆ型化合物の製法 | |
| US3703544A (en) | Process for preparing the tris(hydroxymethyl)-aminomethane salt of pge2 | |
| JPS6034954B2 (ja) | ３，４−メチレンジオキシマンデル酸の製造法 | |
| SU657750A3 (ru) | Способ получени кристаллической модификации натриевой соли 7 цианацетиламино-3-ацетоксиметил3-цефем-4-карбоновой кислоты | |
| US4168376A (en) | Process for crystalline sodium cefamandole | |
| KR840000036B1 (ko) | 옥사-β-락탐 2산 화합물의 D-세스퀴나트륨염의 제조방법 | |
| IL31169A (en) | Penicilloic acid derivatives and process for the manufacture thereof | |
| US4263454A (en) | Lithium ribonate, lithium arabonate and the preparation and purification of these salts | |
| JPS60120859A (ja) | Ｐｇｅ↓２類似体のエステルの製法 | |
| SU454739A3 (ru) | Способ получени 5(6)-ацилбензимидазолилалкилкарбаматов | |
| JPH01153654A (ja) | 含フッ素カルボン酸アンモニウム塩の製造方法 | |
| SU474991A3 (ru) | Способ получени кристаллической соли щелочного металла -карбоксибензилпенициллина | |
| KR810001154B1 (ko) | 5-설파모일-오르트아닐린산의 제조방법 | |
| KR20100128051A (ko) | 클로피도그렐 황산수소염의 결정 형태 ｉ의 선택적 제조방법 | |
| JP2576598B2 (ja) | 光学活性１−メチル−３−フェニルプロピルアミンの製法 | |
| RU218891C (ru) | Способ получени 3-оксиацетилиндола, его эфиров и аналогов | |
| NO132353B (enrdf_load_stackoverflow) | ||
| DK142724B (da) | Fremgangsmåde til fremstilling af fritstrømmende krystaller af tris (hydroxymethyl)aminomethan-saltet af prostaglandin E2. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MA | Patent expired |
Owner name: THE UPJOHN COMPANY |