PL408793A1 - Co-crystal 4-amino-N-(4,6-dimethylpyrimidin-2-yl)-benzene-1-sulfonamide - quinolin-2-carboxylic acid and method for producing it - Google Patents

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

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Publication number
PL408793A1
PL408793A1 PL40879314A PL40879314A PL408793A1 PL 408793 A1 PL408793 A1 PL 408793A1 PL 40879314 A PL40879314 A PL 40879314A PL 40879314 A PL40879314 A PL 40879314A PL 408793 A1 PL408793 A1 PL 408793A1
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PL
Poland
Prior art keywords
sulfonamide
benzene
amino
crystal
carboxylic acid
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PL40879314A
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Polish (pl)
Inventor
Dorota Pogoda
Veneta Videnova-Adrabinska
Jan Janczak
Original Assignee
Politechnika Wrocławska
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Application filed by Politechnika Wrocławska filed Critical Politechnika Wrocławska
Priority to PL40879314A priority Critical patent/PL408793A1/en
Publication of PL408793A1 publication Critical patent/PL408793A1/en

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Abstract

Wynalazek dotyczy kokryształu 4-amino-N-(4,6-dimetylopirymidyn-2-ylo)-benzeno-1-sulfonamid - kwas chinolino-2-karboksylowy o wzorze 1, który znajduje zastosowanie w przemyśle farmaceutycznym. Wynalazek ujawnia również sposób wytwarzania kokryształu o wzorze 1, charakteryzujący się tym, że 0,1 mmol 4-amino-N-(4,6-dimetylopirydymidyn-2-ylo)-benzeno-1 -sulfonamidu i 0,1 mmol kwasu chinolino-2-karboksylowego umieszcza się w moździerzu agatowym, po czym całość uciera się z 1 kroplą rozpuszczalnika wybranego spośród: metanolu, etanolu, acetonitrylu przez około 1 minutę. Całość rozpuszcza się w 8 ml wybranego rozpuszczalnika, miesza szybkością 100-300 rpm przez około 2 do 10 minut w temperaturze pokojowej i tak przygotowany roztwór przesącza, a następnie odparowuje w warunkach temperatury pokojowej, i po 3 do 5 dni. Uzyskuje się pomarańczowe kryształy.The invention relates to a 4-amino-N- (4,6-dimethylpyrimidin-2-yl) -benzene-1-sulfonamide-quinoline-2-carboxylic 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, characterized in that 0.1 mmol of 4-amino-N- (4,6-dimethylpyridimidin-2-yl) benzene-1-sulfonamide and 0.1 mmol of quinoline acid The 2-carboxylic acid 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. It is dissolved in 8 ml of the selected solvent, stirred at 100-300 rpm for about 2 to 10 minutes at room temperature and the solution thus prepared is filtered and then evaporated at room temperature and after 3 to 5 days. Orange crystals are obtained.

PL40879314A 2014-07-10 2014-07-10 Co-crystal 4-amino-N-(4,6-dimethylpyrimidin-2-yl)-benzene-1-sulfonamide - quinolin-2-carboxylic acid and method for producing it PL408793A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL40879314A PL408793A1 (en) 2014-07-10 2014-07-10 Co-crystal 4-amino-N-(4,6-dimethylpyrimidin-2-yl)-benzene-1-sulfonamide - quinolin-2-carboxylic acid and method for producing it

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PL40879314A PL408793A1 (en) 2014-07-10 2014-07-10 Co-crystal 4-amino-N-(4,6-dimethylpyrimidin-2-yl)-benzene-1-sulfonamide - quinolin-2-carboxylic acid and method for producing it

Publications (1)

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PL408793A1 true PL408793A1 (en) 2015-04-13

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PL40879314A PL408793A1 (en) 2014-07-10 2014-07-10 Co-crystal 4-amino-N-(4,6-dimethylpyrimidin-2-yl)-benzene-1-sulfonamide - quinolin-2-carboxylic acid and method for producing it

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PL (1) PL408793A1 (en)

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