Chemical synthesis of flavipucine

Chemistry of carbon compounds – Miscellaneous organic carbon compounds – C-metal

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

424263, C07D21140

Patent

active

040948781

ABSTRACT:
A method for the total chemical synthesis of flavipucine employs the condensation of 4-hydroxy-6-methyl-2-pyridone with isobutylglyoxal in alkali alkoxide. The resulting alkali salt is acylated in both the 1' and 4 positions. Treatment of the 1',4-diacyloxy derivative with excess alkaline peroxide yields flavipucine.

REFERENCES:
girota et al., J. Chem. Soc., Chem. Comm. 1976, pp. 566 to 567.
Chemical Abstracts, vol. 77, abst. No. 114194m (1972) (abst. of Findlay et al., J. Chem. Soc., Perkin Trans. 1 1972, pp. 2071-2074).
Findlay et al., Can. J. Chem. vol. 54, pp. 270 to 274 (1976).
Findlay et al., Synthetic Communications, vol. 3, pp. 355-358 (1973).

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Chemical synthesis of flavipucine does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Chemical synthesis of flavipucine, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Chemical synthesis of flavipucine will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-9405

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.