FIELD: organic chemistry, chemical technology, medicine.
SUBSTANCE: invention relates to a method for preparing new 2,4-dialkylindolo[2,3-h]-1-oxaazulenium chlorides of the general formula (I):
wherein Ia: R is -OCH3; R1 is CH3; Ib: R is hydrogen atom (H); R1 is CH3; Ic: R is -O-CH2-O-; R1 is CH3; Id: R is -O-CH2-CH2-O-; R1 is CH3; Ie: R is -OCH3; R1 is C2H5; If: -O-CH2-O-; R1 is C2H5. Method involves passing gaseous hydrogen chloride through solution of the corresponding 2-acetylaminoarylbis-(5-alkylfur-2-yl)methane of the formula (II):
in methanol at boiling for 80-90 min. Method provides preparing new tetracyclic derivatives eliciting the potential anticancer activity.
EFFECT: improved preparing method, valuable medicinal properties of compounds.
2 tbl, 5 ex
Title | Year | Author | Number |
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|
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NITRATE SALTS OF HYPOTENSIVE MEDICINAL AGENTS | 1999 |
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METHOD OF OBTAINING DERIVATIVES OF N-ACETYL-4-HYDROXY-2METHYL-5-(5-METHYLFUR-2-YL)-1H-BENZO[g]INDOLE | 2008 |
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NAPHTHALENE DERIVATIVES | 2001 |
|
RU2354646C2 |
SPIROIMIDAZOLIDINE DERIVATIVES, METHOD FOR THEIR PREPARING AND PHARMACEUTICAL COMPOSITION BASED ON THEREOF | 2000 |
|
RU2245879C2 |
COLORED POLYSILOXANE-POLYCARBONATES AND METHOD FOR THEIR PREPARING | 2005 |
|
RU2278127C1 |
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RU2119482C1 |
Authors
Dates
2005-01-10—Published
2003-07-07—Filed