NO144138B - APPARATUS FOR THE CONVERSION OF A PREPARABLE MATERIAL TO FIBER - Google Patents

APPARATUS FOR THE CONVERSION OF A PREPARABLE MATERIAL TO FIBER Download PDF

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Publication number
NO144138B
NO144138B NO792844A NO792844A NO144138B NO 144138 B NO144138 B NO 144138B NO 792844 A NO792844 A NO 792844A NO 792844 A NO792844 A NO 792844A NO 144138 B NO144138 B NO 144138B
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NO
Norway
Prior art keywords
preparable
fiber
conversion
oxides
formula
Prior art date
Application number
NO792844A
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Norwegian (no)
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NO792844L (en
NO144138C (en
Inventor
Marcel Levecque
Jean A Battigelli
Dominique Plantard
Original Assignee
Saint Gobain
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
Publication of NO792844L publication Critical patent/NO792844L/en
Application filed by Saint Gobain filed Critical Saint Gobain
Publication of NO144138B publication Critical patent/NO144138B/en
Publication of NO144138C publication Critical patent/NO144138C/en

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    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/536Immunoassay; Biospecific binding assay; Materials therefor with immune complex formed in liquid phase
    • G01N33/537Immunoassay; Biospecific binding assay; Materials therefor with immune complex formed in liquid phase with separation of immune complex from unbound antigen or antibody
    • G01N33/539Immunoassay; Biospecific binding assay; Materials therefor with immune complex formed in liquid phase with separation of immune complex from unbound antigen or antibody involving precipitating reagent, e.g. ammonium sulfate
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B37/00Manufacture or treatment of flakes, fibres, or filaments from softened glass, minerals, or slags
    • C03B37/01Manufacture of glass fibres or filaments
    • C03B37/06Manufacture of glass fibres or filaments by blasting or blowing molten glass, e.g. for making staple fibres

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  • Health & Medical Sciences (AREA)
  • Immunology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Molecular Biology (AREA)
  • Biomedical Technology (AREA)
  • Hematology (AREA)
  • Urology & Nephrology (AREA)
  • General Physics & Mathematics (AREA)
  • Manufacturing & Machinery (AREA)
  • Cell Biology (AREA)
  • Food Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Biotechnology (AREA)
  • Pathology (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Microbiology (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Nonwoven Fabrics (AREA)
  • Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
  • Manufacture, Treatment Of Glass Fibers (AREA)
  • Reinforced Plastic Materials (AREA)
  • Moulding By Coating Moulds (AREA)
  • Preliminary Treatment Of Fibers (AREA)
  • Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
  • Inorganic Fibers (AREA)
  • Glass Compositions (AREA)
  • Surface Treatment Of Glass Fibres Or Filaments (AREA)
  • Glass Melting And Manufacturing (AREA)
  • Laminated Bodies (AREA)

Description

Fremgangsmåte for fremstilling av tuberkulostatisk aktive S-oksyder av "-alkylisothionikotinamider. Process for the production of tuberculostatically active S-oxides of "-alkylisothionicotinamides.

Nærværende oppfinnelse vedrører en fremgangsmåte for fremstilling av hittil ukjente tuberkulostatisk aktive S-oksyder av visse a-alkylisothionikotinamider. The present invention relates to a process for the production of hitherto unknown tuberculostatically active S-oxides of certain α-alkylisothionicotinamides.

Ifølge nærværende oppfinnelse frem-stilles hittil ukjente S-oksyder av a alkylisothionikotinamider med den generelle formel: hvor R betyr en alkylgruppe med tre til fem carbonatomer, ved en fremgangsmåte som består i å oksydere ved hjelp av hydrogenperoksyd et isothionikotinamid med formelen: According to the present invention, hitherto unknown S-oxides are produced from a alkylisothionicotinamides with the general formula: where R means an alkyl group with three to five carbon atoms, by a method which consists in oxidizing with the aid of hydrogen peroxide an isothionicotinamide with the formula:

hvor R er som foran definert. Oksydasjo-nen utføres i et inert organisk eller vandig organisk medium, f. eks. ethanol for-tynnet med vann, fortrinnsvis ved en temperatur under 50° C. where R is as defined above. The oxidation is carried out in an inert organic or aqueous organic medium, e.g. ethanol diluted with water, preferably at a temperature below 50°C.

S-oksyder av a-alkylisothionikitinami-der oppnådd ved fremgangsmåten etter oppfinnelsen er i besiddelse av en tuber-(144138). S-oxides of α-alkylisothionikitinamides obtained by the method according to the invention possess a tuber-(144138).

kulostatisk aktivitet liknende den for de tilsvarende ikke oksyderte forbindelser med formel II og har god gastrisk toleranse. coulostatic activity similar to that of the corresponding non-oxidized compounds of formula II and has good gastric tolerance.

For anvendelse ved behandlingen av tuberkulose kan forbindelsene med den generelle formel I forenes med en farmasøy-tisk bærer, og blandingene fremstilt på i og for seg kjent måte til faste former er egnet for oral administrasjon, slik som granuler eller tabletter eller som suppositorer. I hu-manterapi skal slike blandinger vanligvis administreres slik at de gir et voksent in-divid 0,25 til 1 g aktivt stoff (fortrinnsvis i flere mindre mengder) pr. dag. For use in the treatment of tuberculosis, the compounds of the general formula I can be combined with a pharmaceutical carrier, and the mixtures prepared in a manner known per se into solid forms are suitable for oral administration, such as granules or tablets or as suppositories. In human therapy, such mixtures should usually be administered so that they give an adult individual 0.25 to 1 g of active substance (preferably in several smaller amounts) per day.

De følgende eksempler illustrerer oppfinnelsen. The following examples illustrate the invention.

Eksempel 1. Example 1.

Hydrogenperoksydoppløsning (110 vol. Hydrogen peroxide solution (110 vol.

20 cc) tilsettes i løpet av 20 minutter, uten 20 cc) is added within 20 minutes, without

at temperaturen overskrider 30 °C til en suspensjon av 2-n-propyl-isothionikotinamid (30 g) i absolutt alkohol (318 cc) og vann (17 cc). Etter omrøring i 5 timer er oppløsning praktisk talt komplett og tre-kull (2 g) tilsettes for å spalte det over-skytende hydrogenperoksyd. Et rått produkt (31,1 g) oppnås, etter filtrering og konsentrering under et trykk på 0,1 mm Hg ved en temperatur under 55°C. Ved å rive dette produkt i isopropanol, oppnås 2-n-propyl-isothionikotinamid-S-oksyd (4,45 g), s.p. 117—118°C. that the temperature exceeds 30 °C to a suspension of 2-n-propylisothionicotinamide (30 g) in absolute alcohol (318 cc) and water (17 cc). After stirring for 5 hours, dissolution is practically complete and charcoal (2 g) is added to decompose the excess hydrogen peroxide. A crude product (31.1 g) is obtained, after filtration and concentration under a pressure of 0.1 mm Hg at a temperature below 55°C. Trituring this product in isopropanol gives 2-n-propylisothionicotinamide S-oxide (4.45 g), m.p. 117-118°C.

Ved å gå frem under de samme betin-gelser som dem beskrevet i eksempel 1 og By proceeding under the same conditions as those described in example 1 and

ved å begynne med 2-n-butyl-isothionikotinamid (30 g) oppnås et rått voksliknen-de produkt (33 g), s.p. ca. 75°C. Ved om-krystallisasjon fra ethylacetat oppnås 2-n-butyl-isothionikotinamid-S-oksyd som først starting with 2-n-butylisothionicotinamide (30 g) a crude wax-like product (33 g) is obtained, m.p. about. 75°C. By recrystallization from ethyl acetate, 2-n-butyl-isothionicotinamide-S-oxide is obtained which first

mykner ved 82—84°C, fulgt av størkning og softens at 82—84°C, followed by solidification and

en annen fullstendig smeltning ved 93—94°another complete melting at 93—94°

C. C.

Fremgangsmåte for fremstilling av S-oksyder av a-alkylisothionikotinamider Process for the production of S-oxides of α-alkylisothionicotinamides

overensstemmende med formel I er også consistent with formula I is also

beskrevet i patent nr. 104 677, men fremgangsmåten etter dette er begrenset til described in patent no. 104 677, but the method according to this is limited to

bruken av uorganiske persalter som oksydasjonsmidler, for utgangsmateriale overensstemmende med formel II, reagenser the use of inorganic persalts as oxidizing agents, for starting material conforming to formula II, reagents

som hittil ikke har vært beskrevet som which has not hitherto been described as

oksydasjonsmidler for thioamider. oxidizing agents for thioamides.

Claims (1)

Fremgangsmåte for fremstilling av berkulostatisk aktive S-oksyder av a-alkyl-Process for the preparation of berculostatically active S-oxides of α-alkyl- isothionikotinamider med den generelle formel:isothionicotinamides of the general formula: hvor R betyr en alkylgruppe med tre til fem carbonatomer, karakterisert ved oksydasjon ved hjelp av hydrogenperoksyd av et isothionikotinamid med formelen: hvor R er som foran definert, og oksydasjo-nen utføres fortrinnsvis i et inert organisk eller vandig organisk medium ved en temperatur under 50°C.where R means an alkyl group with three to five carbon atoms, characterized by oxidation with hydrogen peroxide of an isothionicotinamide with the formula: where R is as defined above, and the oxidation is preferably carried out in an inert organic or aqueous organic medium at a temperature below 50°C.
NO792844A 1975-02-18 1979-09-03 APPARATUS FOR THE CONVERSION OF A PREPARABLE MATERIAL TO FIBER NO144138C (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR7504970A FR2384723A1 (en) 1975-02-18 1975-02-18 METHOD AND DEVICES FOR THE MANUFACTURING OF FIBERS FROM THERMOPLASTIC MATERIALS, SUCH AS GLASS

Publications (3)

Publication Number Publication Date
NO792844L NO792844L (en) 1976-08-19
NO144138B true NO144138B (en) 1981-03-23
NO144138C NO144138C (en) 1982-12-06

Family

ID=9151346

Family Applications (2)

Application Number Title Priority Date Filing Date
NO760518A NO142168C (en) 1975-02-18 1976-02-17 APPARATUS FOR THE CONVERSION OF A MELTABLE FIBER MATERIAL TO FIBER.
NO792844A NO144138C (en) 1975-02-18 1979-09-03 APPARATUS FOR THE CONVERSION OF A PREPARABLE MATERIAL TO FIBER

Family Applications Before (1)

Application Number Title Priority Date Filing Date
NO760518A NO142168C (en) 1975-02-18 1976-02-17 APPARATUS FOR THE CONVERSION OF A MELTABLE FIBER MATERIAL TO FIBER.

Country Status (34)

Country Link
JP (1) JPS51105420A (en)
AR (1) AR210752A1 (en)
AT (1) AT367381B (en)
AU (1) AU503308B2 (en)
BE (1) BE838652A (en)
BR (1) BR7600978A (en)
CA (1) CA1075863A (en)
CH (1) CH614686A5 (en)
CS (1) CS209485B2 (en)
DD (1) DD122813A5 (en)
DE (1) DE2606300C2 (en)
DK (1) DK64576A (en)
EG (1) EG11994A (en)
ES (1) ES445155A1 (en)
FI (1) FI59579C (en)
FR (1) FR2384723A1 (en)
GB (1) GB1521343A (en)
HU (1) HU176868B (en)
IE (1) IE43347B1 (en)
IL (1) IL49052A (en)
IN (1) IN144822B (en)
IT (1) IT1055883B (en)
LU (1) LU74363A1 (en)
NL (1) NL7601316A (en)
NO (2) NO142168C (en)
NZ (1) NZ180023A (en)
OA (1) OA05246A (en)
PL (1) PL112503B1 (en)
PT (1) PT64809B (en)
RO (1) RO76342A (en)
SE (1) SE419079B (en)
TR (1) TR19173A (en)
YU (1) YU40076A (en)
ZA (1) ZA76922B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2849357A1 (en) * 1978-11-14 1980-05-29 Saint Gobain METHOD AND DEVICE FOR INFLUENCING THE PROPERTIES OF FIBERS IN THE PRODUCTION OF FIBERS FROM THERMOPLASTIC MATERIAL

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2223318B1 (en) * 1973-03-30 1978-03-03 Saint Gobain

Also Published As

Publication number Publication date
FI59579C (en) 1981-09-10
IE43347L (en) 1976-08-18
PL112503B1 (en) 1980-10-31
HU176868B (en) 1981-05-28
TR19173A (en) 1978-06-16
ZA76922B (en) 1977-01-26
DE2606300C2 (en) 1983-11-17
PT64809A (en) 1976-03-01
AU503308B2 (en) 1979-08-30
IT1055883B (en) 1982-01-11
FI59579B (en) 1981-05-29
BE838652A (en) 1976-08-17
GB1521343A (en) 1978-08-16
CA1075863A (en) 1980-04-22
CS209485B2 (en) 1981-12-31
NO142168B (en) 1980-03-31
NO760518L (en) 1976-08-19
PT64809B (en) 1977-07-11
IE43347B1 (en) 1981-02-11
NZ180023A (en) 1978-07-28
CH614686A5 (en) 1979-12-14
NL7601316A (en) 1976-08-20
NO792844L (en) 1976-08-19
IN144822B (en) 1978-07-15
JPS51105420A (en) 1976-09-18
AR210752A1 (en) 1977-09-15
RO76342A (en) 1981-06-21
IL49052A0 (en) 1976-06-30
DK64576A (en) 1976-08-19
IL49052A (en) 1979-10-31
NO142168C (en) 1981-09-17
ES445155A1 (en) 1977-05-16
FR2384723A1 (en) 1978-10-20
ATA96576A (en) 1981-11-15
NO144138C (en) 1982-12-06
SE419079B (en) 1981-07-13
FI760383A (en) 1976-08-19
BR7600978A (en) 1976-09-14
LU74363A1 (en) 1976-12-31
AT367381B (en) 1982-06-25
DE2606300A1 (en) 1976-08-26
DD122813A5 (en) 1976-11-05
EG11994A (en) 1978-06-30
YU40076A (en) 1982-06-30
FR2384723B1 (en) 1980-05-30
AU1115376A (en) 1977-08-25
OA05246A (en) 1981-02-28
SE7601533L (en) 1976-08-19

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