Ex Parte Krapp et alDownload PDFPatent Trial and Appeal BoardFeb 16, 201712376320 (P.T.A.B. Feb. 16, 2017) Copy Citation United States Patent and Trademark Office UNITED STATES DEPARTMENT OF COMMERCE United States Patent and Trademark Office Address: COMMISSIONER FOR PATENTS P.O.Box 1450 Alexandria, Virginia 22313-1450 www.uspto.gov APPLICATION NO. FILING DATE FIRST NAMED INVENTOR ATTORNEY DOCKET NO. CONFIRMATION NO. 12/376,320 02/04/2009 Michael Krapp 074012-0116-US-286410 5676 123223 7590 02/21/2017 Drinker Biddle & Reath LLP (WM) 222 Delaware Avenue, Ste. 1410 Wilmington, DE 19801-1621 EXAMINER HOLT, ANDRIAE M ART UNIT PAPER NUMBER 1616 NOTIFICATION DATE DELIVERY MODE 02/21/2017 ELECTRONIC Please find below and/or attached an Office communication concerning this application or proceeding. The time period for reply, if any, is set in the attached communication. Notice of the Office communication was sent electronically on above-indicated "Notification Date" to the following e-mail address(es): IPDocketWM @ dbr.com penelope. mongelluzzo @ dbr. com DB RIPDocket @ dbr. com PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE BEFORE THE PATENT TRIAL AND APPEAL BOARD Ex parte MICHAEL KRAPP, RAINER BERGHAUS, MATTHIAS BRATZ, ELMAR KIBLER, and HERVE R. VANTIEGHEM1 Appeal 2015-007595 Application 12/376,320 Technology Center 1600 Before ERIC B. GRIMES, RICHARD J. SMITH, and RACHEL H. TOWNSEND, Administrative Patent Judges. GRIMES, Administrative Patent Judge. DECISION ON APPEAL This is an appeal under 35U.S.C. § 134 involving claims to herbicide- containing concentrate, which have been rejected as obvious. We have jurisdiction under 35 U.S.C. § 6(b). We reverse. STATEMENT OF THE CASE Claims 17, 21, 30, 31, and 33—38 are on appeal. Claim 17 is the only independent claim and reads as follows (emphasis added): 1 Appellants identify the Real Party in Interest as BASF SE. (Appeal Br. 2.) Appeal 2015-007595 Application 12/376,320 17. A non-aqueous active compound concentrate comprising a) from 10 to 100 g/1 of at least one 4-benzoyl-substituted pyrazole compound of the formula I or one of its salts in which R1 and R5 are each methyl; R3 is methylsulfonyl; R2 is 4,5- dihydroisoxazol-3-yl; and R4 and R6 are hydrogen, b) from 400 to 700 g/1 of 2-chloro-N-(2,4-dimethyl-3-thienyl)-N- (2-methoxy-1 -methylethyl)acetamide, and c) from 10 to 200 g/1 of at least one surfactant S selected from a mixture of at least one anionic surfactant and at least one nonionic surfactant, where the components a), b) and c) are present dissolved in a mixture of organic solvents containing at least 95% by weight, based on the solvent mixture, of dl) at least one aprotic polar organic solvent having a miscibility with water at 25°C and 1 bar of at least 50 g/1, which is selected from the group consisting of dimethyl sulfoxide, N- methylpyrrolidone, N-ethylpyrrolidone, and mixtures thereof, and d2) at least one organic solvent having a solubility in water at 25°C and 1 bar of less than 5 g/1, which is a hydrocarbon solvent; in which the anionic surfactant is selected from the group consisting of compounds comprising at least one SO3 group or one PO4 group and at least one aliphatic hydrocarbon radical having 8 to 22 carbon atoms or an araliphatic hydrocarbon radical having 10 to 24 carbon atoms and in which the nonionic surfactant comprises, as main component, at least one poly-C2- C3-alkylene glycol ether compound, where the weight ratio of apolar protic [sic, aprotic polar] solvent to hydrocarbon solvent is from 1:10 to 10:1, and where the total amount of organic solvent is from 300 to 600 g/1. Components a) and b) of the claimed composition are known as topramezone and dimethenamid, respectively. (Spec. 1: 46-47, 4:41—45.) o R 2 Appeal 2015-007595 Application 12/376,320 DISCUSSION The Examiner has rejected all of the claims on appeal under 35 U.S.C. § 103(a) as obvious based on Sievemich2 and Aven.3 (Ans. 2.) The Examiner finds that Sievemich discloses synergistic mixtures comprising two herbicides, where topramezone and dimethenamid are particularly preferred. {Id. at 3 4.) The Examiner finds that Sievemich discloses that hydrocarbons and N-methylpyrrolidone are suitable inert auxiliaries for use in its composition, and that Sievemich also discloses suitable surfactants. {Id. at 4—5.) The Examiner finds that Aven teaches an emulsifiable concentrate for crop protection active agents, including dimethenamid, that comprises an organic solvent, a polar aprotic solvent, and a surfactant system that includes a nonionic surfactant and an anionic surfactant. {Id. at 6.) The Examiner concludes that it would have been obvious to modify Sievemich’s composition to include the solvent mixture and surfactants disclosed by Aven. {Id. at 7—9.) Appellants argue, among other things, that the “claimed concentrate requires that component dl) and component d2) of the recited solvent mixture account for at least 95% of the total solvent present in the concentrate” and the Examiner has not shown where this limitation is disclosed in the references. (Appeal Br. 18.) Appellants point out that Aven discloses that its composition also includes adjuvants, which are described as alcohol ethoxylates and therefore would be recognized by a person of 2 Sievemich et al., US 6,534,444 Bl, issued March 18, 2003. 3 Aven, EP 1023833 A2, published August 2, 2000. 3 Appeal 2015-007595 Application 12/376,320 ordinary skill in the art as common organic solvents. (Id. at 18—19.) Appellants argue that “Aven’s adjuvants, which are present from 150 to 500 g/1, when combined with Aven’s teaching of the inclusion of 80 to 300 g/1 of an aprotic polar solvent and 150 to 400 g/1 of an organic hydrocarbon solvent, describe a concentrate in which there exist at least three very different classes of co-solvents.” (Id. at 19.) Appellants argue that, when the amounts of all three solvents are considered, the percentage of organic solvent and polar aprotic solvent is less than 95% of the total solvent. (Id.) The Examiner agrees that “Aven does teach that one or more adjuvants are used in the formulation and that these adjuvants are selected from known solvents.” (Ans. 12.) The Examiner reasons, however, that the claims “use the transitional phrase ‘comprising’ which indicates that other components can be added to the formulation. Therefore, it would have been obvious to the skilled artisan that other solvent classes can be added to the formulation.” (Id. at 13.) That is, “the instant claims do not indicate that the polar solvent and the organic solvent have to be 95% by weight of all solvents present,” only that the polar aprotic solvent(s) and organic solvent(s) are made up of at least 95% of one of the specific solvents or type of solvents listed in the claim. (Id.) We agree with Appellants, however, that the Examiner’s claim interpretation is broader than is reasonable based on the claim language read in light of the Specification. The disputed limitation reads as follows: “where the components a), b) and c) are present dissolved in a mixture of organic solvents containing at least 95% by weight, based on the solvent mixture.” The claim thus requires that the topramezone, dimethenamid, and 4 Appeal 2015-007595 Application 12/376,320 surfactants (components a), b), and c)) are “dissolved in a mixture of organic solvents,” where the mixture contains at least 95%, by weight of the solvent mixture, components dl) and d2). The plain meaning of the claim language is that the solvent mixture in which components a), b), and c) are dissolved contains at least 95% of components dl) and d2). Although the Examiner is correct that another solvent can be present (Ans. 13), the claim language limits such other solvent(s) to no more than 5% of the solvent mixture. Aven discloses an emulsifiable concentrate that contains, among other things, “150 to 500 g/1 of one or more adjuvants,” “optionally one or more organic solvents,” and “a water-miscible polar aprotic solvent.” (Aven | 6.) Aven states that “[sjuitable adjuvants [] are selected from the group consisting of alcohol alkoxylates and water-immiscible N-alkyl- pyrrolidones, preferably N-C3 15 alkyl-pyrrolidones, in particular N-octyl- pyrrolidone or N-dodecyl-pyrrolidone.” (Id. 129.) The Examiner finds that Aven’s “adjuvants are selected from known solvents.” (Ans. 12.) Thus, Aven’s compositions contain at least 150 g/1 of adjuvant/solvent. Aven discloses specific embodiments that contain up to 400 g/1 of organic solvent and 80 to 300 g/1 of polar aprotic solvent. (Aven H 50—51.) These compositions thus can contain no more than 82% of combined organic solvent and polar aprotic solvent.4 Even Aven’s broadest description of its composition still requires at least 150 g/1 of adjuvant(s) (id. | 6), and in order for that amount to be no more than 5% of the total solvent, 4 400 g/1 organic solvent plus 300 g/1 polar aprotic solvent plus 150 g/1 of adjuvant is 850 g/1 of total solvents, of which 700 g/1 is organic solvent or polar aprotic solvent; 700/850 = 0.82. 5 Appeal 2015-007595 Application 12/376,320 the amount of organic solvent and polar aprotic solvent would have to be at least 3000 g/1, which is much more than is used in any of Aven’s specifically described embodiments. (See id. at || 50-51, 62—78.) In summary, we agree with Appellants that the Examiner has not shown that the limitation of “components a), b) and c). . . dissolved in a mixture of organic solvents containing at least 95% by weight, based on the solvent mixture,” of components dl) and d2) would have been obvious to a person of ordinary skill in the art based on the cited references. We therefore reverse the rejection on appeal. REVERSED 6 Copy with citationCopy as parenthetical citation