FI57404C - Foerfarande foer framstaellning av nya n-substituerade cykloseriner - Google Patents
Foerfarande foer framstaellning av nya n-substituerade cykloseriner Download PDFInfo
- Publication number
- FI57404C FI57404C FI2237/74A FI223774A FI57404C FI 57404 C FI57404 C FI 57404C FI 2237/74 A FI2237/74 A FI 2237/74A FI 223774 A FI223774 A FI 223774A FI 57404 C FI57404 C FI 57404C
- Authority
- FI
- Finland
- Prior art keywords
- amino
- isoxazolidone
- methyl
- cycloserine
- reaction
- Prior art date
Links
- 230000001351 cycling effect Effects 0.000 title 1
- DYDCUQKUCUHJBH-UHFFFAOYSA-N D-Cycloserine Natural products NC1CONC1=O DYDCUQKUCUHJBH-UHFFFAOYSA-N 0.000 claims description 15
- 229960003077 cycloserine Drugs 0.000 claims description 15
- DYDCUQKUCUHJBH-UWTATZPHSA-N D-Cycloserine Chemical compound N[C@@H]1CONC1=O DYDCUQKUCUHJBH-UWTATZPHSA-N 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 101000913968 Ipomoea purpurea Chalcone synthase C Proteins 0.000 claims 1
- 101000907988 Petunia hybrida Chalcone-flavanone isomerase C Proteins 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 18
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 16
- 239000000243 solution Substances 0.000 description 14
- -1 cycloserine compound Chemical class 0.000 description 11
- 238000001914 filtration Methods 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000000047 product Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Natural products CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- HWYHDWGGACRVEH-UHFFFAOYSA-N n-methyl-n-(4-pyrrolidin-1-ylbut-2-ynyl)acetamide Chemical compound CC(=O)N(C)CC#CCN1CCCC1 HWYHDWGGACRVEH-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- TZMFJUDUGYTVRY-UHFFFAOYSA-N ethyl methyl diketone Natural products CCC(=O)C(C)=O TZMFJUDUGYTVRY-UHFFFAOYSA-N 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/04—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Communicable Diseases (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US38454573A | 1973-08-01 | 1973-08-01 | |
| US38454573 | 1973-08-01 | ||
| US47316474 | 1974-05-28 | ||
| US05/473,164 US3932439A (en) | 1973-08-01 | 1974-05-28 | N-substituted cycloserine compounds, salts thereof, and processes for preparing them |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI223774A7 FI223774A7 (en:Method) | 1975-02-02 |
| FI57404B FI57404B (fi) | 1980-04-30 |
| FI57404C true FI57404C (fi) | 1980-08-11 |
Family
ID=27010648
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI2237/74A FI57404C (fi) | 1973-08-01 | 1974-07-23 | Foerfarande foer framstaellning av nya n-substituerade cykloseriner |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US3932439A (en:Method) |
| JP (1) | JPS59513B2 (en:Method) |
| AR (1) | AR209591A1 (en:Method) |
| AT (1) | AT333753B (en:Method) |
| BG (1) | BG24229A3 (en:Method) |
| CA (1) | CA1039292A (en:Method) |
| CH (1) | CH603607A5 (en:Method) |
| CS (1) | CS197235B2 (en:Method) |
| DD (1) | DD114081A5 (en:Method) |
| DE (1) | DE2436960A1 (en:Method) |
| DK (1) | DK383374A (en:Method) |
| EG (1) | EG11488A (en:Method) |
| ES (1) | ES428535A1 (en:Method) |
| FI (1) | FI57404C (en:Method) |
| FR (1) | FR2239247B1 (en:Method) |
| GB (1) | GB1426310A (en:Method) |
| HK (1) | HK86579A (en:Method) |
| IE (1) | IE39639B1 (en:Method) |
| IL (1) | IL45334A (en:Method) |
| LU (1) | LU70633A1 (en:Method) |
| NL (1) | NL184834C (en:Method) |
| NO (1) | NO141896C (en:Method) |
| PL (1) | PL91504B1 (en:Method) |
| RO (1) | RO63457A (en:Method) |
| SE (1) | SE406588B (en:Method) |
| SU (1) | SU545259A3 (en:Method) |
| YU (1) | YU37160B (en:Method) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63107977A (ja) * | 1986-05-21 | 1988-05-12 | Takeda Chem Ind Ltd | イソオキサゾロン誘導体 |
| DE4034713A1 (de) * | 1990-11-01 | 1992-05-07 | Bayer Ag | 3-oxy-substituierte isoxazoline, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung von endoparasiten |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2773878A (en) * | 1952-03-05 | 1956-12-11 | Pfizer & Co C | Cycloserine and production thereof |
-
1974
- 1974-05-28 US US05/473,164 patent/US3932439A/en not_active Expired - Lifetime
- 1974-07-15 NL NLAANVRAGE7409571,A patent/NL184834C/xx not_active IP Right Cessation
- 1974-07-17 DK DK383374A patent/DK383374A/da not_active Application Discontinuation
- 1974-07-17 JP JP49081225A patent/JPS59513B2/ja not_active Expired
- 1974-07-18 SE SE7409378A patent/SE406588B/xx not_active IP Right Cessation
- 1974-07-18 NO NO742622A patent/NO141896C/no unknown
- 1974-07-23 YU YU2053/74A patent/YU37160B/xx unknown
- 1974-07-23 FI FI2237/74A patent/FI57404C/fi active
- 1974-07-23 IL IL45334A patent/IL45334A/en unknown
- 1974-07-23 IE IE1565/74A patent/IE39639B1/xx unknown
- 1974-07-23 ES ES428535A patent/ES428535A1/es not_active Expired
- 1974-07-24 CH CH1021974A patent/CH603607A5/xx not_active IP Right Cessation
- 1974-07-24 FR FR7425654A patent/FR2239247B1/fr not_active Expired
- 1974-07-24 GB GB3271674A patent/GB1426310A/en not_active Expired
- 1974-07-30 LU LU70633A patent/LU70633A1/xx unknown
- 1974-07-30 AR AR254951A patent/AR209591A1/es active
- 1974-07-30 DD DD180199A patent/DD114081A5/xx unknown
- 1974-07-30 CA CA205,980A patent/CA1039292A/en not_active Expired
- 1974-07-30 AT AT624774A patent/AT333753B/de not_active IP Right Cessation
- 1974-07-31 CS CS745447A patent/CS197235B2/cs unknown
- 1974-07-31 PL PL1974173137A patent/PL91504B1/pl unknown
- 1974-07-31 BG BG027391A patent/BG24229A3/xx unknown
- 1974-07-31 SU SU2048524A patent/SU545259A3/ru active
- 1974-07-31 DE DE2436960A patent/DE2436960A1/de not_active Withdrawn
- 1974-08-01 RO RO7400079636A patent/RO63457A/ro unknown
- 1974-08-03 EG EG315/74A patent/EG11488A/xx active
-
1979
- 1979-12-20 HK HK865/79A patent/HK86579A/xx unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP3421354B2 (ja) | 結晶性セフジニルアミン塩 | |
| CZ288657B6 (cs) | Nová krystalová modifikace hydrochloridu 1-cyklopropyl-7-([S,S]-2,8-diazabicyklo[4.3.0]non-8-yl)-6-fluor-1,4-dihydro-8-methoxy-4-oxo-3-chinolinkarboxylové kyseliny, způsob její výroby a použití pro výrobu léčiv | |
| NO151876B (no) | Fremgangsmaate og anordning for foring av dyr | |
| NO341136B1 (no) | Fremgangsmåte for fremstilling av triazol substituerte azaindoloksoeddikpiperazinderivater | |
| ES2879294T3 (es) | Formas polimórficas de Belinostat y procesos para la preparación de las mismas | |
| JP4268871B2 (ja) | ピリミジノン化合物及びその薬剤として許容される塩の製造方法 | |
| JP2004520446A (ja) | ロサルタンカリウムの結晶化方法 | |
| FI57404C (fi) | Foerfarande foer framstaellning av nya n-substituerade cykloseriner | |
| SU558644A3 (ru) | Способ получени имидазолов или их солей | |
| IL25315A (en) | O-(2-guanidino-ethyl)-oximes | |
| SU417944A3 (ru) | Способ получения алкалоидов | |
| FI62095C (fi) | Foerfarande foer framstaellning av nya 1- och d1-6-/m-(isoxazol-3-karboxiamido)fenyl)-2,3,5,6-tetrahydroimidazo(2,1-b)tiazolderivat vilka anvaends som maskmedel | |
| JP3253245B2 (ja) | グアニジン誘導体の製造法、新規中間体およびその製造法 | |
| US3758546A (en) | Methoxy amine derivatives and process for preparing them | |
| SU1371490A3 (ru) | Дефолиирующее средство | |
| JPS62286968A (ja) | 新規ニコチン酸アミド誘導体 | |
| BRPI0822432B1 (pt) | "processo para a preparação de composto intermediário para sintetizar um antiulcerante" | |
| JP2012523392A (ja) | ピリミジン誘導体の調製プロセス | |
| US2538139A (en) | Biotin derivatives and processes of preparing the same | |
| RU2084441C1 (ru) | Способ получения кислотно-аддитивных солей труднорастворимых карбоновых кислот и аминов или аминокислот | |
| US2697095A (en) | Penicillin salts of glycine-diphenylamides | |
| KR800001289B1 (ko) | 2-아닐리노-옥사졸린의 제조방법 | |
| RU2427574C2 (ru) | Моногидрохлориды и натриевые соли таутомерных 5(6)-алкоксикарбониламинопроизводных 2-арил-1-гидроксибензимидазол-3-оксида с высокой противогрибковой активностью и способ их получения | |
| WO2023006986A1 (en) | Method for preparing and purifying an agent suitable for treating anemia | |
| CA1036495A (en) | Imidazole diagnostic agents |