Patent Application
20120083594
1. Field of the Invention
The invention relates to a process of preparing the (B—C) disaccharide intermediate, a building block for the preparation of polysaccharides, and more particularly fondaparinux.
2. Description of the Related Art
Fondaparinux (A—B—C—D—E) is a heparin sulfated pentasaccharide with anticoagulant activity and a linear sequence is required for binding to antithrombin III (ATIII). Because fondaparinux is a synthetic compound, it is considered a safer medication than the traditional anticoagulant, heparin or LMWH (low-molecular-weight heparin).
U.S. Pat. No. 4,818,816 discloses processes for preparing the (B—C) disaccharide building block of fondaparinux. However, the selectivity is not good enough and the compound needs to be purified by column chromatography, which is not suitable for use in an industrial process.
The present invention provides a novel process for preparing the intermediate of the (B—C) disaccharide building block of fondaparinux (A—B—C—D—E). The selectivity of the process is 100%. In addition, the compound obtained by the process could be purified by crystallization. The present invention is more suitable for use in an industrial process.
The present invention provides a compound of formula (I)
wherein
R1 is selected from the group consisting of alkylacyl, arylacyl and alkylarylacyl, or substituted alkylacyl, arylacyl and alkylarylacyl; carbonate, and carbamate;
R2 is an oxygen-protecting group;
R3 and R4 are independently selected from hydrogen, methyl, C2-C5 alkyl, phenyl and aryl.
Compound (I) above can be used in preparing the intermediate of B—C disaccharide building block of fondaparinux.
Preferably, R1 is benzoyl.
Preferably, R2 is selected from the group consisting of 4-methoxyphenyl; benzyl, substituted benzyl; alkylacyl, arylacyl and alkylarylacyl, or substituted alkylacyl, arylacyl and alkylarylacyl; and carbonate.
The present invention also provides a process for preparing the compound of formula (I) by glycosylation of compound of formula (II)
with the compound of formula (III)
wherein
R1, R2, R3 and R4 are as defined for compound of formula (I); and X1 is a leaving group.
Preferably, X1 is selected from thioalkyl, thioaryl, halogen, imidoyl, 4-penten-1-yloxy and the stereochemistry may be alpha or beta. More preferably, X1 is thiocresyl.
The above glycosylation is preferably conducted in the presence of an activator and a solvent. Preferably, the activator is a sulfonic acid, sulfonate, silyl sulfonate, N-iodosuccinimide (NIS), or a mixture thereof, more preferably, the activator is NIS, trifluoromethanesulfonic acid (TfOH), or Trimethylsilyl triflate (TMSOTf). Preferably, the solvent is an aprotic solvent, and more preferably the solvent is dichloromethane (DCM) and acetonitrile (ACN).
Compound (I) can be used for preparing (B—C)′ disaccharide. (B—C)′ disaccharide can be applied for preparing polysaccharides generally, and more particularly, fondaparinux by using the “BC+A+DE” or “BC+DE+A” synthetic strategy where (B—C)′, (B—C)″, (D—E)′ and (D—E)″ represent the β-anomeric disaccharides.
The present process has several advantages: (1) higher efficiency in the glycosylation of compound (II) and (III) (high yield and exclusive stereoselectivity), as only β-anomeric disaccharide is produced; (2) a convenient synthetic process from compound (I) to (B—C)′; (3) the preparation of compound (II) is easier than the method disclosed in U.S. Pat. No. 4,818,816; (4) less protecting groups on the C unit are used, resulting in less waste.
Charged (IIa) (7.65 g, 1.2 eq.), (III) (1.62 g, 1 eq.) and molecular sieve (MS, 3 g, 1 part) in dry DCM (50 mL, 5 part), the mixture was stirred for 30 min. To the reaction mixture is added N-iodosuccinimide (NIS) (15.6 g, 1.1 eq.) and the mixture was cooled to −40° C., and TfOH (0.4 mL, 0.2 eq.) was added. The reaction mixture was stirred at −50˜−40° C. for 1 hr. After the reaction was finished, Et3N (0.4 mL) was added and stirred for 10 min. The reaction mixture was filtered and washed with DCM (14 mL, 5 part). The filtrate was washed with 10% Na2S2O3(aq) (4 part), and concentrated. Crystallization from DCM/n-heptane gave (Ia) (5.7 g, 87%)
Charged (Ia) (9.0 g, 1 eq.) in THF (45 mL, 5 part) and added 30% NaOMe solution (4.1 mL, 1.5 eq.). The mixture was stirred for 30 min at 4˜6° C. After the reaction was completed, the mixture was added to amberlite to neutralize the solution and remove solvent to afford the oily intermediate (Ib). After washed by NaCl(aq), the (Ib) was dissolved in THF and cooled to 0˜5° C. and added NaH (1.83 g of a 60% suspension in oil, 3 eq.), TBAI (0.56 g, 0.1eq.). The mixture was stirred for 10 min and benzyl bromide (4.5 mL, 2.5eq.) was added. The mixture was stirred for 3 h at rt, water was added, and the mixture was evaporated. Extraction with DCM and crystallization from DCM/n-heptane gave (Ic) (7.1 g, 80%).
Charged (Ic) (7.0 g, 1 eq.) in DMF/H2O (10/1 mL) and added NaN3 (4.0 g, 5 eq.). The mixture was stirred for 24 hr at 120° C. After the reaction was completed, the mixture was extracted with ethyl acetate. The organic layer was evaporated to afford crude (Id). Then, crude (Id) was dissolved in pyridine (6 mL, 0.8 part) and added Ac2O (3 mL, 0.4 part). The mixture was stirred for 16 hr at rt. After the reaction was completed, the mixture was extracted with ethyl acetate and washed by NaHCO3(aq). The solvent of pyridine was co-evaporated with toluene three times. The organic phase was concentrated and the residue was purified by column chromatography to give (Ie) (6.3 g, 78%).
Charged (Ie) (6.3 g, 1 eq.) in 80% AcOH(aq) (60 mL). The mixture was stirred for 5 hr at 70° C. After the reaction was completed, the solvent was removed by vacuum. The mixture was extracted with ethyl acetate and washed by NaHCO3(aq). The organic layer was concentrated and the residue was purified by column chromatography to give (If) (5.3 g, 97%).
Charged (If) (4.0 g, 1 eq.) in DCM/H2O (40/20 mL) and added 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) (220 mg, 0.2 eq.) and [bis(acetoxy)iodo]benzene (BAIB) (6.8 g, 3 eq.). The reaction mixture was stirred at room temperature for 1 hr. The reaction was monitored by TLC. After the reaction was finished, the reaction mixture was washed with 10% Na2S2O3(aq) and extracted with ethyl acetate. The organic layer was concentrated to give the acid intermediate (Ig) without further purification. Then, charged crude (Ig) in DMF (40 mL) and added K2CO3 (660 mg, 0.64 eq.) and Mel (1.1 mL, 2.5 eq.). The reaction mixture was stirred at room temperature for 16 hr. The reaction was monitored by TLC. After the reaction was finished, the reaction mixture was extracted with ethyl acetate and washed by NaCl(aq). The organic layer was concentrated and the residue was purified by column chromatography to give (Ih) (3.4 g, 80%).
The present application claims priority from U.S. Provisional Patent Application Ser. No. 61/389,844, filed on Oct. 5, 2010, the contents of which is herein incorporated by reference.
| Number | Date | Country | |
|---|---|---|---|
| 61389844 | Oct 2010 | US |
