Efficient and scalable process for the manufacture of fondaparinux sodium
View Patent ↗The present invention relates to a process for the synthesis of the Factor Xa anticoagulent Fondaparinux and related compounds. The invention relates, in addition, to efficient and scalable processes for the synthesis of various intermediates useful in the synthesis of Fondaparinux and related compounds.
1. A process for the preparation of a monosaccharide AMod3 having the structure
comprising anhydro ring opening and acetylating the monomer IntA5 having the structure
to form a compound AMod 1 having the structure
and α-methylglycosylating the monomer AMod1 to form the monomer AMod3.
2. A process for the preparation of Fondaparinux sodium compound IntB1 having the structure
comprising the step of:
(a) benzylating the compound SM-B having the structure
3. The process of claim 2 , further comprising the steps:
(i) selectively hydrolyzing the compound IntB1 to form a compound IntB2 having the structure
(ii) oxidatively cleaving the 5,6 dihydroxy group of the compound IntB2 to form a compound IntB3 having the structure
(iii) reacting the compound IntB3 with tris(phenylthio) methane to form a compound IntB4 having the structure
(iv) esterifying the compound IntB4 to form a compound IntB5 having the structure
(v) cleaving the 1,2-isopropylidene group of the compound IntB5 to form a compound IntB6 having the structure
and
(vi) reacting the compound IntB6 with 2-methoxy propene to form Monomer B-1 having the structure
4. A process for preparing EDC-Trimer-CB of the formula
comprising the steps:
(a) coupling an E monomer having the structure
to a DC Building Block having the structure
to obtain EDC-Trimer-CB.