FIELD: medicine.
SUBSTANCE: present invention refers to a compound for treating neurodegenerative diseases and pain, a method for preparing it and compositions based thereon. Disclosed is a compound having the following structure:
or its pharmaceutically acceptable salt, where X is Cl or Br. Disclosed method comprises a step of reacting 6-chloropurinurbofuranoside in the presence of a base with an appropriately substituted (thienyl)methanamine, or first obtaining (2',3'-O-isopropylidene) adenosine derivative containing a hydroxyl-protecting group, then obtaining (2',3'-O-isopropylidene) adenosine derivative containing a hydroxyl-protecting group and an amino-protecting group which is reacted with the corresponding thienyl derivative 7:
,
where X is Cl or Br and Y is X, OH, methanesulfonate (OSO2CH3, OMs), p-toluenesulfonate (OSO2C6H4-p-CH3, OTs), or trifluoromethanesulfonate (OSO2CF3, OTf), after which protective groups are removed.
EFFECT: novel compounds effective in treating neurodegenerative diseases and pain, effective methods for preparing them and compositions based thereon.
17 cl, 7 ex, 10 dwg
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Authors
Dates
2019-07-23—Published
2014-10-22—Filed