PL408794A1 - Co-crystal 4-amino-N-(4,6-dimethylpyrimidin-2-yl)-benzene-1-sulfonamide - 4-nitrophenyl acetic acid and method for producing it - Google Patents

Co-crystal 4-amino-N-(4,6-dimethylpyrimidin-2-yl)-benzene-1-sulfonamide - 4-nitrophenyl acetic acid and method for producing it

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Publication number
PL408794A1
PL408794A1 PL40879414A PL40879414A PL408794A1 PL 408794 A1 PL408794 A1 PL 408794A1 PL 40879414 A PL40879414 A PL 40879414A PL 40879414 A PL40879414 A PL 40879414A PL 408794 A1 PL408794 A1 PL 408794A1
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PL
Poland
Prior art keywords
sulfonamide
benzene
amino
crystal
dimethylpyrimidin
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PL40879414A
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Polish (pl)
Inventor
Dorota Pogoda
Veneta Videnova-Adrabinska
Jan Janczak
Original Assignee
Politechnika Wrocławska
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Publication date
Application filed by Politechnika Wrocławska filed Critical Politechnika Wrocławska
Priority to PL40879414A priority Critical patent/PL408794A1/en
Publication of PL408794A1 publication Critical patent/PL408794A1/en

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pyridine Compounds (AREA)

Abstract

Wynalazek dotyczy kokryształu 4-amino-N-(4,6-dimetylopirymidyn-2-ylo)-benzeno-1-sulfonamid - kwas 4-nitrofenylooctowy o wzorze 1, który znajduje zastosowanie w przemyśle farmaceutycznym. Wynalazek ujawnia również sposób wytwarzania kokryształu o wzorze 1, polegający na tym, że 0,1 mmol 4-amino-N-(4,6-dimetylopirydymidyn-2-ylo)-benzeno-1-sulfonamidu i 0,1 mmol kwasu 4-nitrofenylooctowego umieszcza się w moździerzu agatowym, po czym całość uciera się z 1 kroplą rozpuszczalnika wybranego spośród: metanolu, etanolu, acetonitrylu przez około 1 minutę. Następnie całość rozpuszcza się w 8 - 10 ml wybranego rozpuszczalnika, miesza szybkością 100 - 300 rpm przez około 2 do 10 minut w temperaturze w zakresie od 30 do 60°C, a klarowny roztwór pozostawia w celu powolnego odparowania rozpuszczalnika w warunkach temperatury pokojowej. Po czym po 2 do 4 dniach uzyskuje się żółte kryształy, które następnie przemywa się 5 ml aprotonowym rozpuszczalnikiem.The invention relates to a 4-amino-N- (4,6-dimethylpyrimidin-2-yl) -benzene-1-sulfonamide-4-nitrophenylacetic acid co-crystal of formula 1 which is used in the pharmaceutical industry. The invention also discloses a method for producing a co-crystal of Formula 1, wherein 0.1 mmol of 4-amino-N- (4,6-dimethylpyridimidin-2-yl) benzene-1-sulfonamide and 0.1 mmol of 4- nitrophenylacetate is placed in an agate mortar and the whole is triturated with 1 drop of a solvent selected from methanol, ethanol, acetonitrile for about 1 minute. The whole is then dissolved in 8-10 ml of the selected solvent, mixed at 100-300 rpm for about 2 to 10 minutes at a temperature in the range of 30 to 60 ° C, and the clear solution is allowed to slowly evaporate the solvent at room temperature. After 2 to 4 days yellow crystals are obtained, which are then washed with 5 ml aprotic solvent.

PL40879414A 2014-07-10 2014-07-10 Co-crystal 4-amino-N-(4,6-dimethylpyrimidin-2-yl)-benzene-1-sulfonamide - 4-nitrophenyl acetic acid and method for producing it PL408794A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL40879414A PL408794A1 (en) 2014-07-10 2014-07-10 Co-crystal 4-amino-N-(4,6-dimethylpyrimidin-2-yl)-benzene-1-sulfonamide - 4-nitrophenyl acetic acid and method for producing it

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PL40879414A PL408794A1 (en) 2014-07-10 2014-07-10 Co-crystal 4-amino-N-(4,6-dimethylpyrimidin-2-yl)-benzene-1-sulfonamide - 4-nitrophenyl acetic acid and method for producing it

Publications (1)

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PL408794A1 true PL408794A1 (en) 2015-04-13

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PL40879414A PL408794A1 (en) 2014-07-10 2014-07-10 Co-crystal 4-amino-N-(4,6-dimethylpyrimidin-2-yl)-benzene-1-sulfonamide - 4-nitrophenyl acetic acid and method for producing it

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PL (1) PL408794A1 (en)

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