PL428569A1 - Flavanone analog and method of its preparation - Google Patents

Flavanone analog and method of its preparation

Info

Publication number
PL428569A1
PL428569A1 PL428569A PL42856919A PL428569A1 PL 428569 A1 PL428569 A1 PL 428569A1 PL 428569 A PL428569 A PL 428569A PL 42856919 A PL42856919 A PL 42856919A PL 428569 A1 PL428569 A1 PL 428569A1
Authority
PL
Poland
Prior art keywords
flavanone
analog
preparation
precipitate
ethanol
Prior art date
Application number
PL428569A
Other languages
Polish (pl)
Other versions
PL238431B1 (en
Inventor
Anna Sykuła
Paulina Błazińska
Elżbieta Łodyga-Chruścińska
Original Assignee
Politechnika Łódzka
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
Application filed by Politechnika Łódzka filed Critical Politechnika Łódzka
Priority to PL428569A priority Critical patent/PL238431B1/en
Publication of PL428569A1 publication Critical patent/PL428569A1/en
Publication of PL238431B1 publication Critical patent/PL238431B1/en

Links

Landscapes

  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Przedmiotem wynalazku jest analog flawanonu, o nazwie chemicznej (E)-N'-(2-fenylochroman-4-ylideno)izonikotynohydrazyd, o przedstawionym wzorze. Analog ten otrzymuje się w reakcji flawanonu z izoniazydem w środowisku bezwodnego etanolu w obecności stężonego kwasu siarkowego (VI) w temperaturze 60°C w czasie 24 godzin, po czym mieszaninę reakcyjną z wytrąconym osadem pozostawia się do wystudzenia, a następnie wytrącony osad produktu sączy się pod próżnią i przemywa etanolem i destylowaną wodą.The invention relates to a flavanone analog having the chemical name (E) -N '- (2-phenylchroman-4-ylidene) isonicotinohydrazide having the formula shown. This analogue is obtained by reacting flavanone with isoniazid in anhydrous ethanol in the presence of concentrated sulfuric acid (VI) at a temperature of 60 ° C for 24 hours, then the reaction mixture with a precipitate is allowed to cool, and then the precipitate of the product is filtered off. under vacuum and washed with ethanol and distilled water.

PL428569A 2019-01-14 2019-01-14 Flavanone analog and method of its preparation PL238431B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL428569A PL238431B1 (en) 2019-01-14 2019-01-14 Flavanone analog and method of its preparation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PL428569A PL238431B1 (en) 2019-01-14 2019-01-14 Flavanone analog and method of its preparation

Publications (2)

Publication Number Publication Date
PL428569A1 true PL428569A1 (en) 2020-07-27
PL238431B1 PL238431B1 (en) 2021-08-23

Family

ID=71733860

Family Applications (1)

Application Number Title Priority Date Filing Date
PL428569A PL238431B1 (en) 2019-01-14 2019-01-14 Flavanone analog and method of its preparation

Country Status (1)

Country Link
PL (1) PL238431B1 (en)

Also Published As

Publication number Publication date
PL238431B1 (en) 2021-08-23

Similar Documents

Publication Publication Date Title
NO120582B (en)
MX2022013045A (en) Synthesis of cantharidin.
SA519410408B1 (en) Method for preparing intermediate of 4-methoxypyrrole derivative
PL422926A1 (en) 7-propoxy-naringenin oxime and method for obtaining 7-propoxy-naringenin oxime
PL422932A1 (en) 7-isopropoxy-naringenin oxime and method for obtaining 7-isopropoxy-naringenin oxime
PL422935A1 (en) 7,4'-didecanoxy-naringenin oxime and method for obtaining 7,4'-didecanoxy-naringenin oxime
EA202192581A1 (en) D-METHYROSINE COMPOSITIONS AND METHODS FOR THEIR PRODUCTION
PL434616A1 (en) 7,4'-di-O-hexylnaringenin oxime and method of its preparation
PL428571A1 (en) Flavanone analog and method of its preparation
Buu-Hoï et al. NN′-Diarylthioureas and related compounds of potential biological interest
PL428568A1 (en) Flavanone analog and method of its preparation
US20140275624A1 (en) Preparation of 4-amino-2,4-dioxobutanoic acid
Burtles et al. LXXXVI.—The relation of pilocarpidine to pilocarpine. Synthesis of 1: 4-and 1: 5-dimethylglyoxalines
ES2367086T3 (en) AN IMPROVED PROCEDURE FOR THE PREPARATION OF NEVIRAPINA.
PL426156A1 (en) 4-iodophenyl-1-(4-methylimidazol-5-yl)thiosemicarbazide derivatives, method of their preparation and medical use
CN106008653A (en) Acylhydrazone glycyrrhetinate derivative as well as preparation method and application thereof
US2780623A (en) Method of preparing thioammeline
Ishidate et al. The Cleavage of Camphor Ring. V. 7-Hydroxy-π-apocamphane and 1-Hydroxy-10-apocamphor.
CHAN et al. A New Phytochemical Survey of Malaysia. IV. Chemical Screening
US2430006A (en) 4-methyl-5-imidazolone-(2)-caproic acid and esters thereof
PL443477A1 (en) 7,4'-di-O-undecylnaringenin oxime and method of obtaining 7,4'-di-O-undecylnaringenin oxime
PL419744A1 (en) 4'-Amino-4-carboxychalcone and method for obtaining 4'-amino-4-carboxychalcone
US2552026A (en) Production of amino nitriles by ammonolysis of chloro nitriles
PL421031A1 (en) 7-ethoxy-naringenin-oxime and method for obtaining 7-ethoxy-naringenin-oxime
PL422936A1 (en) 7,4'-diisopropoxy-naringenin oxime and method for obtaining 7,4'-diisopropoxy-naringenin oxime