PL410357A1 - Gamma 2-[(5-nitro-2-furanyl)-methylene]-hydraziecarboxamide form and method for producing it - Google Patents

Gamma 2-[(5-nitro-2-furanyl)-methylene]-hydraziecarboxamide form and method for producing it

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Publication number
PL410357A1
PL410357A1 PL410357A PL41035714A PL410357A1 PL 410357 A1 PL410357 A1 PL 410357A1 PL 410357 A PL410357 A PL 410357A PL 41035714 A PL41035714 A PL 41035714A PL 410357 A1 PL410357 A1 PL 410357A1
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PL
Poland
Prior art keywords
furanyl
nitro
methylene
carboxamide
hydrazine
Prior art date
Application number
PL410357A
Other languages
Polish (pl)
Other versions
PL224685B1 (en
Inventor
Dorota Pogoda
Veneta Videnova-Adrabińska
Original Assignee
Politechnika Wrocławska
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.)
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Publication date
Application filed by Politechnika Wrocławska filed Critical Politechnika Wrocławska
Priority to PL410357A priority Critical patent/PL224685B1/en
Publication of PL410357A1 publication Critical patent/PL410357A1/en
Publication of PL224685B1 publication Critical patent/PL224685B1/en

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Abstract

Wynalazek dotyczy odmiany ? 2-[(5-nitro-2-furanylo)-metyleno]-hydrazyno-karboksyamidu o wzorze 1, która znajduje zastosowanie w przemyśle farmaceutycznym. Ujawniono również sposób wytwarzania formy ? 2-[(5-nitro-2-furanylo)-metyleno]-hydrazyno-karboksyamidu o wzorze 1, który polega na tym, że do 0,100 mmol 2-[(5-nitro-2-furanylo)-metyleno]-hydrazyno-karboksyamidu dodaje się 4-6 ml rozpuszczalnika polarnego wybranego z grupy: metanol, etanol, propan-1-ol, propan-2-ol, butan-2-ol lub acetonitryl i miesza się na mieszadle magnetycznym z szybkością 100 - 300 rpm w temperaturze 60-80°C przez 10-20 minut, po czym klarowny roztwór ochładza się do temperatury 25-30°C i pozostawia do powolnego odparowania rozpuszczalnika w warunkach temperatury pokojowej, w wyniku czego po 2 do 5 dni uzyskuje się gotowy produkt w postaci żółtych kryształów.The invention relates to a variation? 2 - [(5-nitro-2-furanyl) methylene] hydrazine carboxamide of formula 1, which is used in the pharmaceutical industry. Also disclosed is a method for making the mold? 2 - [(5-nitro-2-furanyl) -methylene] -hydrazine-carboxamide of formula 1, which consists in that up to 0.100 mmol of 2 - [(5-nitro-2-furanyl) -methylene] -hydrazine carboxamide 4-6 ml of polar solvent selected from the group: methanol, ethanol, propan-1-ol, propan-2-ol, butan-2-ol or acetonitrile are added and mixed on a magnetic stirrer at a speed of 100 - 300 rpm at temperature 60-80 ° C for 10-20 minutes, after which the clear solution is cooled to 25-30 ° C and allowed to evaporate slowly at room temperature, resulting in a finished product in the form of yellow after 2 to 5 days crystals.

PL410357A 2014-12-04 2014-12-04 Gamma 2-[(5-nitro-2-furanyl)-methylene]-hydraziecarboxamide form and method for producing it PL224685B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL410357A PL224685B1 (en) 2014-12-04 2014-12-04 Gamma 2-[(5-nitro-2-furanyl)-methylene]-hydraziecarboxamide form and method for producing it

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PL410357A PL224685B1 (en) 2014-12-04 2014-12-04 Gamma 2-[(5-nitro-2-furanyl)-methylene]-hydraziecarboxamide form and method for producing it

Publications (2)

Publication Number Publication Date
PL410357A1 true PL410357A1 (en) 2016-01-18
PL224685B1 PL224685B1 (en) 2017-01-31

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Family Applications (1)

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PL410357A PL224685B1 (en) 2014-12-04 2014-12-04 Gamma 2-[(5-nitro-2-furanyl)-methylene]-hydraziecarboxamide form and method for producing it

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PL224685B1 (en) 2017-01-31

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