(-3-ketotetrahydrofuran-2-yl) ethanal derivatives and a method for their preparation
AssigneeBioCure, Inc.
InventorNeil Geddes Clarkson Hendry
Life of this patent
Estimating the term…
Loading patent…
AssigneeBioCure, Inc.
InventorNeil Geddes Clarkson Hendry
Estimating the term…
Compounds having utility in medicine in countering cellular malfunction e.g. in conditions embraced by the general term "cancer", which compounds normally exist us a keto-enol tautomeric pair, the racetalc keto form of which is rapresented by formula (Ia), wherein R is a hydrogen, lower alkyl, acyl, or another functional group of up to 6 carbons including at least one hetero atom, which atom may be directly bonded to the .beta.-carbon, which compound may be in the acylic form shown or in a cyclic form as equilibrium keto-enol tautomer derivatives and anomeric forms thereof, including enantiomers when R is hydrogen and diastereoisomers when R is another group. A method of obtaining such a compound comprises selecting an appropriate dihydrofuran having a protected primary alcohol side chain in the 2-position, subjecting the said protected alcohol side chain-substituted dihydrofuran to oxidation using a chromium-based reagent to yield the corresponding acid, subjecting said acid to iodolaetonisation conditions to yield the cis,cis,trans-trisubstituted iodo-lactone which upon displacement of the iodine provides the cis,cis,cis-tri-substituted hydroxylacetone which is capable of being reduced to obtain a lactol which is in equilibrium with the corresponding open chain aldehyde. ##STR1##
A compound of the formula (Ia) in which the compound normally exists as a keto-enol tautomeric pair, the racemic keto form of which is represented by the formula ##STR3## wherein R is a hydrogen, hydroxyl, lower alkyl, acyl, or another functional group of up to 6 carbons including at least one hetero atom, which atom may be directly bonded to the .beta.-carbon.
A method of obtaining (3-ketotetrahydrofuran-2-yl)ethanal comprising subjecting trans-hexen-3-ene-1,6-diol to an iodo-etherification reaction to give the corresponding 3-iodotetrahydrofuran which retains the free .alpha.-hydroxyl, using a protective group to protect said .alpha.-hydroxyl during a subsequent reaction to displace the iodine yielding the cis 3-hydroxytetrahydrofuran which upon deprotection and Swern oxidation provides the desired racemic (3-ketotetrahydrofuran-2-yl)ethanal.
Dependencies are inferred from the claim text.