NO124306B - - Google Patents
Download PDFInfo
- Publication number
- NO124306B NO124306B NO487569A NO487569A NO124306B NO 124306 B NO124306 B NO 124306B NO 487569 A NO487569 A NO 487569A NO 487569 A NO487569 A NO 487569A NO 124306 B NO124306 B NO 124306B
- Authority
- NO
- Norway
- Prior art keywords
- chloro
- alkali metal
- disulfonamide
- compounds
- metal salts
- Prior art date
Links
- 238000000034 method Methods 0.000 claims description 10
- 229910052783 alkali metal Inorganic materials 0.000 claims description 8
- -1 alkali metal salts Chemical class 0.000 claims description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 4
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 claims description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
- 208000010412 Glaucoma Diseases 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- RJMGUEXGQXNUBI-UHFFFAOYSA-N 5-chloro-4-hydroxybenzene-1,3-disulfonyl chloride Chemical compound OC1=C(Cl)C=C(S(Cl)(=O)=O)C=C1S(Cl)(=O)=O RJMGUEXGQXNUBI-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- GJQPMPFPNINLKP-UHFFFAOYSA-N diclofenamide Chemical compound NS(=O)(=O)C1=CC(Cl)=C(Cl)C(S(N)(=O)=O)=C1 GJQPMPFPNINLKP-UHFFFAOYSA-N 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- DELKNGSNILXDSN-UHFFFAOYSA-N 4,5-dichlorobenzene-1,3-disulfonyl chloride Chemical compound ClC1=CC(S(Cl)(=O)=O)=CC(S(Cl)(=O)=O)=C1Cl DELKNGSNILXDSN-UHFFFAOYSA-N 0.000 description 1
- WKDNROIOJLGMTQ-UHFFFAOYSA-N 5-bromo-4-chlorobenzene-1,3-disulfonamide Chemical compound NS(=O)(=O)C1=CC(Br)=C(Cl)C(S(N)(=O)=O)=C1 WKDNROIOJLGMTQ-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 241000282472 Canis lupus familiaris Species 0.000 description 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-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
- 241001465754 Metazoa Species 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000973 chemotherapeutic effect Effects 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 230000007665 chronic toxicity Effects 0.000 description 1
- 231100000160 chronic toxicity Toxicity 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 239000002934 diuretic Substances 0.000 description 1
- 230000001882 diuretic effect Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 231100000636 lethal dose Toxicity 0.000 description 1
- 231100000225 lethality Toxicity 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000001452 natriuretic effect Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000011287 therapeutic dose Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 231100000816 toxic dose Toxicity 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F9/00—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments
- D01F9/08—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments of inorganic material
- D01F9/12—Carbon filaments; Apparatus specially adapted for the manufacture thereof
- D01F9/14—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments
- D01F9/20—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products
- D01F9/21—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products from macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D01F9/22—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products from macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyacrylonitriles
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Inorganic Fibers (AREA)
- Artificial Filaments (AREA)
- Carbon And Carbon Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19681816170 DE1816170A1 (de) | 1968-12-20 | 1968-12-20 | Verfahren zur Herstellung von Kohle- oder Graphitfasern |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO124306B true NO124306B (zh) | 1972-04-04 |
Family
ID=5716975
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO487569A NO124306B (zh) | 1968-12-20 | 1969-12-10 |
Country Status (8)
| Country | Link |
|---|---|
| AT (1) | AT295023B (zh) |
| BE (1) | BE743458A (zh) |
| CH (1) | CH515853A (zh) |
| DE (1) | DE1816170A1 (zh) |
| FR (1) | FR2026637A1 (zh) |
| GB (1) | GB1232186A (zh) |
| NL (1) | NL6918783A (zh) |
| NO (1) | NO124306B (zh) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS602408B2 (ja) * | 1977-08-17 | 1985-01-21 | 東邦ベスロン株式会社 | 耐熱酸化性の優れた炭素繊維 |
-
1968
- 1968-12-20 DE DE19681816170 patent/DE1816170A1/de not_active Withdrawn
-
1969
- 1969-12-09 CH CH1828369A patent/CH515853A/de not_active IP Right Cessation
- 1969-12-10 NO NO487569A patent/NO124306B/no unknown
- 1969-12-10 AT AT1149969A patent/AT295023B/de not_active IP Right Cessation
- 1969-12-11 FR FR6942969A patent/FR2026637A1/fr not_active Withdrawn
- 1969-12-15 NL NL6918783A patent/NL6918783A/xx unknown
- 1969-12-19 BE BE743458D patent/BE743458A/xx unknown
- 1969-12-19 GB GB1232186D patent/GB1232186A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB1232186A (zh) | 1971-05-19 |
| BE743458A (zh) | 1970-06-19 |
| AT295023B (de) | 1971-12-27 |
| NL6918783A (zh) | 1970-06-23 |
| DE1816170A1 (de) | 1970-09-17 |
| FR2026637A1 (zh) | 1970-09-18 |
| CH515853A (de) | 1971-11-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69810652T2 (de) | Verfahren um diaryl-pyridine zu herstellen, die als cox-inhibitoren verwendbar sind | |
| IL44061A (en) | 4,5,6,7-tetrahydro-furo(or thieno)(3,2-c)pyridines their preparation and pharmaceutical compositions containing the | |
| NO140424B (no) | Analogifremgangsmaate for fremstilling av farmakologisk aktive indolderivater | |
| EP3023410B1 (en) | 5-BROMINE-2-(alpha-HYDROXYPENTYL)BENZOIC ACID SODIUM SALTS IN DIFFERENT CRYSTAL FORMS, AND PREPARATION METHOD THEREOF | |
| DE2359536A1 (de) | 2,6-diaminonebularinderivate | |
| JPS6126546B2 (zh) | ||
| US2835702A (en) | Benzene 1, 3 disulfonamides possessing diuretic properties | |
| ES2209110T3 (es) | Nuevos derivados de acidos aninoalcano sulfonicos, fosfonicos y fosfinicos, su preparacion y su uso como medicamentos. | |
| NO124306B (zh) | ||
| CH653026A5 (it) | Derivati diazolidinici, loro preparazione ed utilizzazione. | |
| US2678311A (en) | Theophylline salts | |
| NO137236B (no) | Analogifremgangsm}te til fremstilling av et terapeutisk virksomt piperazinyl-pyrimidin-derivat. | |
| JPS602295B2 (ja) | ２−プロピル吉草酸ピバロイルオキシメチル、その製法および抗てんかん剤または鎮痙剤 | |
| US2539854A (en) | Alkaloid salts of n-formyl-s-benzyl d-penicillamine and preparation thereof | |
| LU83497A1 (de) | Amidderivate der p-isobutylphenylpropionsaeure,ihre herstellung und diese enthaltende arzneimittel | |
| US3825590A (en) | Hydroxy-hydroxymethyl-substituted phenylalanine derivatives | |
| JPH0348906B2 (zh) | ||
| US2578761A (en) | Alkanolamine salts of sulfaquinoxaline | |
| SU674672A3 (ru) | Способ получени производных 1,4 -дитиепино-(2,3-с)-пиррола или их солей | |
| US2721203A (en) | Chloral nicotinamide and method for preparing the same | |
| Field et al. | Organic Disulfides and Related Substances. XI. Bisalkylidene,-alkylene, and-arylene Disulfides Containing 2-Aminoethyl Moieties1 | |
| US3980707A (en) | Methylamino derivative of 2-ethylindandione-1,3 and the hydrochloride thereof | |
| SU535293A1 (ru) | Аренсульфогидразиды оксалогидроксамовой кислоты,про вл ющие сахароснижающую активность | |
| US2566038A (en) | Water-soluble sulfonamides | |
| Amundsen et al. | The Preparation of Amino Ethers and Diamines from Chloromethyl Ether and Butadiene1 |