Sunday 22 February 2015

NEW PATENT........WO 2015021902, Novel apixaban crystal form and preparation method thereof



 Apixaban.svgAPIXABAN






NEW PATENT       WO-2015021902
Novel apixaban crystal form and preparation method thereof
2y-Chem Ltd


Apixaban (BMS-562247-01, tradename Eliquis) is an anticoagulant for the treatment of venous thromboembolic events. It is a direct factor Xa inhibitor. Apixaban has been available in Europe since May 2012. An FDA decision on apixaban which was expected on June 28, 2012 was delayed.

On August 21, 2014, Pfizer announced that Apixaban was now FDA approved for treatment and secondary prophylaxis of DVT and PE. It is being developed in a joint venture by Pfizer and Bristol-Myers Squibb.

Novel crystalline polymorphic form A of apixaban, useful for treating venous thromboembolism. Appears to be the first filing by the assignees on this API, which was originally developed and launched by Bristol-Myers Squibb and Pfizer. 

Apixaban is protected by two patent families, that from WO0039131 (where it is first disclosed generically as part of the Markush formula) and that from WO03026652 (claimed specifically). Family members of WO03026652 have SPC protection until May 2026 and expire in the US in 2023 with US154 extension. 

Disclosed are an apixaban A-type crystal form and a preparation method thereof. A diffraction characteristic peak and a differential scanning calorimetry characteristic peak of X-ray powder thereof are respectively shown in FIG. 1 and FIG. 2. The A-type crystal form in the present invention is stable and nonhygroscopic, has a simple preparation method, and has excellent repetition.

The drug also has NCE exclusivity till 2017.







.

Sunday 15 February 2015

WO 2015014031 new patent on Duloxetine, Enzymeworks,Inc., 苏州汉酶生物技术有限公司


Duloxetine2DCSD.svgDuloxetine3DanJ.gif




WO 2015014031 


Biological preparation method of (S)-3-(dimethylamino)-1-(thiophene-2-radical)-1-propyl alcohol by EnzymeWorks Inc
Enzymeworks,Inc., 苏州汉酶生物技术有限公司

https://patentscope.wipo.int/search/en/detail.jsf?docId=WO2015014031

The present invention relates to a biological preparation method of (S)-3-(dimethylamino)-1-(thiophene-2-radical)-1-propyl alcohol. According to the method, (S)-3-(dimethylamino)-1-(thiophene-2-radical)-1-acetone or salt thereof is used as a substrate, and the substrate is subjected to asymmetric reduction reaction in the presence of biocatalyst, cofactor and hydrogen donor to produce (S)-3-(dimethylamino)-1-(thiophene-2-radical)-1-propyl alcohol. Particularly, the biocatalyst is a combination of ketoreductase (KRED) and glucose dehydrogenase, the hydrogen donor is glucose, and the asymmetric reduction reaction is conducted at pH 6.8-7.0 and 25ºC-35ºC. Compared with the biological method in the prior art, the present invention has higher processing stability, and is simpler, more efficient and safer. During the reaction, the generation of highly toxic organic solvents such as acetone can be avoided, the application principle of green chemistry is met, and industrialized application is facilitated.

Enzyme catalyzed synthesis of (S)-3-(dimethylamino)-1-(thiophene-2-radical)-1-propanol, by asymmetric reduction of its corresponding ketone, using ketoreductase and glucose dehydrogenase. Useful as an intermediate in synthesis of duloxetine (first claimed in EP273658), which was developed and launched by Eli Lilly, in collaboration with Shionogi and ex-licensee Boehringer Ingelheim. 

The advantage of the present process is its high efficiency and green chemistry approach in synthesis of the drug. Follows on from WO2014094462, claiming a similar method for preparing duloxetine intermediates.
Duloxetine (Duloxetine) is a low side effect, can effectively treat mental disorders and metabolic disorders drugs (US 5,023,269).The key is to obtain the synthesis of duloxetine intermediates contain a chiral center (S) -3- (dimethylamino) -1- (thiophen-2-yl) -1-propanol (DMAA). Thus the asymmetric reduction of 3- (dimethylamino) -1- (thiophen-2-yl) -1-propanone (DMAK) to give the intermediate is one of the most effective, most studied methods. In achieving this pathway chemical reduction method, due to the need catalytic ruthenium metal catalyst through reaction with hydrogen, its economy, safety and environmental friendliness does not meet the needs of production. Use of chiral resolving agents as chemical resolving agent split method, due to low yield and poor economic reasons, it can not serve as the main production methods. Therefore, the use of enzymatic reduction target product, with its high efficiency and environmental friendliness has become the most effective method.

[5]
In the biological reduction method, U.S. Patent US 2010/0151534 A1 discloses a ketoreductase (KRED) produced (S) -3- (dimethylamino) -1- (thiophen-2-yl) -1- propanol method, the process requires strict control of temperature and reaction, and adding isopropanol, while the reaction of the need to introduce the negative reaction of acetone to remove byproducts, complex operation, it is difficult to repeat, and acetone are dangerous goods, easy volatile, flammable.

[6]
SUMMARY

[7]
Technical problem to be solved by the present invention is to overcome the deficiencies of the prior art, to provide an improved (S) -3- (dimethylamino) -1- (thiophen-2-yl) -1-propanol biological Methods.

[8]
To solve the above technical problem, the present invention takes the following technical solutions: one (S) -3- (dimethylamino) -1- (thiophen-2-yl) -1-propanol biological preparation method, the method 3- (dimethylamino) -1- (thiophen-2-yl) -1-propanone (DMAK) or a salt thereof as a substrate, so that the substrate in the presence of a biocatalyst, cofactor, and a hydrogen donor asymmetric reduction reaction of (S) -3- (dimethylamino) -1- (thiophen-2-yl) -1-propanol, wherein the biological catalyst is ketoreductase (KRED) and glucose dehydrogenase combination, the hydrogen donor is glucose, the asymmetric reduction reaction at a pH of 6.8 to 7.0 and a temperature of 25 ℃ ~ 35 ℃ in performed.

[9]
According to a particular embodiment of the invention embodiment, the biocatalyst, a hydrogen donor, cofactors, substrates feed weight ratio can be 0.02 to 0.1: 1.5 to 6: 0.01 to 0.1: 1, preferably 0.04 to 0.08: 1.5 to 3 : 0.01 to 0.05: 1.

[10]
Preferably, the biocatalyst ketoreductase and glucose dehydrogenase weight ratio of 1: 1 ~ 3. More preferably, the ketoreductase and glucose dehydrogenase weight ratio of 1: 2.

[11]
According to a preferred embodiment of the present invention, may be a cofactor NAD / NADH or NADP / NADPH.

[12]
Asymmetric reduction reaction temperature is preferably from 28 ℃ ~ 32 ℃. Asymmetric reduction reaction is preferably carried out in an aqueous buffer phase.
Figure PCTCN2013083235-appb-I000001


WO2014094462

http://www.google.com/patents/WO2014094462A1?cl=en


Example one
Three to 50 mL reaction flask add 1.0 g substrate MMAK and 1.2g glucose, 8 mL reaction flask again with a good pH of 7.0,0.1 M triethanolamine buffer. Placed in 30 ℃, 900 r / min magnetic stirring water bath with stirring and treated with 2 M NaOH solution to adjust pH to 7.0. When the temperature was stabilized, the reaction flask was added 0.95 mL solution of 20 mg ketoreductase, 31 mg GDH triethanolamine buffer. PH adjusted to 7.0 with NaOH, and washed with 0.95 mL triethanolamine buffer was added to the reaction flask. To the reaction flask was added 100 μL of a solution of 0.5 mg NADP triethanolamine buffer, the reaction started. The reaction temperature was maintained at 30 ℃. The pH of the reaction solution was added dropwise 2 M NaOH solution was adjusted by a pH titrator. Control pH 7.0, initial control point 6.5, final control point is 6.99. HPLC assay for controlling timing of sampling. Reaction 23 h, the conversion rate of> 99%.
Example two
Add 100.0 g and 120.0 g of substrate MMAK glucose into the reactor, was added to the reaction flask with 800 mL of a good pH 7.0,0.1 M triethanolamine buffer. Placed in 30 ℃, mechanically stirred water bath with stirring and treated with 2 M NaOH solution to adjust pH to 7.0. When the temperature was stabilized, the reaction flask was added 95 mL a solution of 2 g ketoreductase, 3.1 g GDH triethanolamine buffer. PH adjusted to 7.0 with NaOH, and washed with 95 mL of triethanolamine buffer was added to the reaction flask. To the reaction flask with 10 mL of a solution of 50 mg NADP triethanolamine buffer, the reaction started. The reaction temperature was maintained at 30 ℃. The pH of the reaction solution was added dropwise 2 M NaOH solution was adjusted by a pH titrator. Control pH 7.0, initial control point 6.5, final control point is 6.99. HPLC assay for controlling timing of sampling. Reaction 23 h, the conversion rate of> 98%.


Figure PCTCN2013083235-appb-I000001
CN101613672A *Aug 4, 2009Dec 30, 2009南京工业大学;南京同凯兆业生物技术有限责任公司Recombined Escherichia coli used for preparing (S)-4-chloro-3-hydroxybutanoate by asymmetric transformation and construction method thereof
CN101993828A *Nov 8, 2010Mar 30, 2011江南大学Method for improving transformation efficiency of (S)-phenyl glycol by coupling glucose-6-phosphate dehydrogenase and (S)-carbonyl reductase
CN102206686A *Apr 19, 2011Oct 5, 2011华东理工大学Preparation method of methyl (R)-o-chloromandelate utilizing biocatalytic asymmetric reduction
US20080220484 *Sep 14, 2006Sep 11, 2008Basf AktiengesellschaftReducing substituted alkanones such as 3-methylamino-1-(2-thienyl)-propan-1-one; biosynthesis; expression cassettes; host cells; for production of duloxetine

...............


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Saturday 14 February 2015

Gilead v. Natco – Gilead’s patent invalid for obviousness-type double patenting





Gilead v. Natco – Gilead’s patent invalid for obviousness-type double patenting


Gilead owns U.S. Patents 5,763,483 and 5,952,375, directed to antiviral compounds and their methods of use. The two patents have the same inventorship and are said to have similar subject matter, but they do not claim priority to a common patent application. The ‘375 patent was filed earlier and issued later than the ‘483 patent. Because of the difference in the earliest file dates, the ‘483 patent expires 22 months later than the ‘383 patent. The filing, issue, and expiration dates are mapped as:
Gilead-patent-timefr
Natco filed an ANDA for a drug covered by the ‘483 patent, and Natco’s only defense when sued for infringement of the ‘483 patent was obviousness-type double patenting, i.e., the assertion that the ‘483 patent was an obvious variation over the ‘375 patent that improperly sought to extend the right to exclude past the expiration of the ‘375 patent.
The district court held for Gilead, concluding that a later-issued but earlier-expiring patent cannot serve as a double patenting reference to an earlier-issued but later-expiring patent, and rejected Natco’s double patenting invalidity defense.
The Federal Circuit majority (Chen and Prost, opinion by Chen) reversed and remanded (Rader dissented). The majority’s reversal is predicated on an assumption that the ‘483 patent is an obvious variation of the ‘375 patent, but the details of that conclusion are not discussed. However, the substantive issue of whether the two patents were obvious variants was not the issue here. Rather, this case on appeal turned on the narrow legal question: “Can a patent that issues after but expires before another patent qualify as a double patenting reference for that other patent?” The answer: Yes.
Gilead’s defense of its patents was that the ‘375 patent does not extend the term of exclusivity for the ‘483 patent because the ‘375 patent issued later. The majority dismisses this argument, stating that in the post-June 8, 1995 Uruguay Round (“URAA”) era, patent expiration dates should control the analysis, not patent issue dates. The panel was concerned over “gamesmanship” in patent expiries if Gilead’s argument was accepted, such as filing serial applications on obvious variations. The panel also points to potential irrational outcomes under Gilead’s arguments. For example, if the ‘375 patent hypothetically issued one day before the ‘483 patent, under Gilead’s argument the extra 22 months of patent life of the ‘483 patent would be improper. This could encourage gamesmanship in applicants’ orchestrating patent issue dates, and is contrary to the intent of Congress in the URAA.
The majority states that the ‘483 patent should have been subject to a terminal disclaimer based on the ‘375 patent according to MPEP § 804.I.B.1.
The panel concludes that looking to the earliest patent expiration for patents that are obvious variants “best fits and serves the purpose of the doctrine of double patenting.” Accordingly, an earlier-expiring patent can qualify as an obviousness-type double patent reference for a later-expiring patent under the circumstances of this case. The expiration of the ‘375 patent should trigger “the public’s right to use the invention claimed in it and all obvious modifications of that invention.” Reversed and remanded.
Rader’s dissent asserts that majority decision is an unwarranted expansion of the judicially created doctrine of obviousness-type double patenting. Rader makes general remarks that the court should be more cautious before articulating a “new rule.”
Rader makes two good points. First, if the ‘375 patent never issued, there would be no question of the validity of the full term of the ‘483 patent. Second, Rader points out that the later filing date of the ‘483 patent is subject to ten months of intervening prior art. But Rader doesn’t really tie these points into an argument that the majority was wrong.
Rader also makes policy objections to the majority holding, including that a disclaimer on the ‘375 patent reduces the risk of multiple assignees asserting essentially the same claims against accused infringers, which is not a danger here, and that no one possesses an affirmative right to practice claimed subject matter.
Ultimately, it appears that Rader’s objection is whether the ‘483 patent was an obvious variant of the ‘383 patent. He defers to the examiner, stating that subsequent improvements, if satisfying the criteria for patentability, could “bar the public from practicing some subject matter encompassed by the expiring patents.” But then he concedes that patentably indistinct claims should not bar the public. Rader makes no specific objection to the majority’s reasoning and stops short of saying he would have affirmed the district court.

In the URAA (post June 8, 1995) era, patent expirations must control this kind of analysis. The district court’s reasoning (and Gilead’s defense of its patents) was essentially based on the old 17-year expiration mindset, that patent expiration followed patent issue dates in lock step. That of course is no longer how the system works.
On the specific facts here, it would be more satisfying if the issue of obviousness was discussed, but presumably that will be taken up on remand.
ref
http://www.google.com/patents/US5952375







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