Application of Robert L. Clarke

356 F.2d 987, 53 C.C.P.A. 954
Court of Customs and Patent Appeals·Decided March 10, 1966·No. Patent Appeal 7489·Published·Cited by 20 cases

Opinions

MARTIN, Judge.

The issue in this appeal from the Board of Appeals is whether Rule 131 affidavits that show certain facts about species of a claimed genus, and that also allege conception of the genus, are sufficient to antedate indirectly a reference disclosing a different species within the claimed genus. This issue arises with respect to generic claims 1 and 2 in appellant’s application serial No. 836,911, filed August 31, 1959, for “1,2-Diacylhexahy-dropyridazines and Preparation Thereof.”

The claims read:

1. 1,2-Diacylhexahydropyridazine in which each acyl is -CO-R wherein R is a member of the group consisting of hydrogen and a hydrocarbon radical having from one to nine carbon atoms.
2. 1,2-Bis (lower-alkanoyl) hexahydropyridazine.

The hexahydropyridazines are a type of bis-amides which are disclosed as having antiviral and diuretic activity with low toxicity in mammals. Structurally, the compounds may be represented thus:

The definition of R as “hydrocarbon” is disclosed in the application as:

* * * In the above general formula * * *, when the R’s represent separate radicals, they are preferably identical. When R represents a hydrocarbon radical, it preferably stands for an aliphatic hydrocarbon radical, either saturated or unsaturated, straight or branched; a cy-cloalkyl radical; a monocarbocyclic aromatic hydrocarbon radical; or a combination of the foregoing radicals. Thus, included in the definition of R are alkyl, for example, methyl, ethyl, propyl, isopropyl, bu-tyl, tertiary-butyl, hexyl, octyl and nonyl; alkenyl, for example, vinyl, 1-propenyl, allyl, 3-hexenyl and 4-octenyl; alkynyl, for example, ethy-nyl, propargyl and 3-hexynyl; cyclo-alkyl, for example, cyclopropyl, cy-[989] clobutyl, cyclopentyl, cyclohexyl, 4-methylcyelohexyl, 2,6-dimethylcyclo-hexyl, and cyclooctyl; cycloalkylalkyl, for example, eyclopentylethyl and cyclohexylmethyl; monocarbocyclic aryl, for example, phenyl, p-tolyl, 3,5-dimethylphenyl and 3-ethylphenyl; and monocarbocyclic aryl-loweralkyl, for example, benzyl, 2-phenylethyl and 3-phenylpropyl. (Emphasis ours.]

Appellant further discloses a genus of compounds, having the same properties, in which the two R’s of the above structure can be joined to form an alpha, beta-lower-alkylene bridge (hereinafter referred to as bridge compounds) .1

The reference relied on by the Patent Office as an anticipation within the meaning of 35 U.S.C. § 102(a), is a publication of Stetter et al. (Stetter) appearing in Vol. 91 of Chemiche Berichte, pp. 1982-8, under date of September 15, 1958. Since that date of publication is less than one year prior to the application date herein there is no question of a statutory time bar under 35 U.S.C. § 102(b). It is acknowledged by appellant that since Stetter shows a compound which falls within the scope of the generic claim it is an anticipation, provided Stetter is available as a reference.

Referring to the structure diagrammed above, Stetter shows a compound in which the R groups are each isopropyl (Stetter’s Compound VII), and a second compound in which the two R groups taken together are an ethylene bridge between the amide groups, thus forming a second ring (Stet-ter’s Compound XI). Stetter shows Compound VII to be an intermediate in a chemical synthesis which can be described broadly as the preparation of cyclic diamines by opening the rings of intermediate bicyclic compounds.2

In an attempt to remove Stetter as a reference under section 102(a), appellant filed a first affidavit under Rule 131 that shows reduction to practice, prior to the effective date of Stetter, of two compounds in which R in the structure shown above is respectively methyl and phenyl, and also an ethylene bridge compound, Stetter’s Compound XI. On the basis of that showing, the examiner allowed four claims: claim 3, a broad or “generic” claim to bridge compounds which includes the bridge Compound XI of Stetter; and three species claims, claim 4 to the methyl species, claim 5 to the phenyl species, both of these being species within rejected claim 1, and claim 6 specifically to the bridge compound, Compound XI of Stetter.

The first affidavit did not, however, relate to the isopropyl species, the Stet-ter Compound VII, which falls within the scope of claims 1 and 2 on appeal. Since the examiner considered that affidavit insufficient to remove the generic claim 1 and 2 anticipating Compound VII, appellant filed a second affidavit which alleges conception of the generic invention prior to the effective date of Stetter. Apparently appellant cannot, or cares not to show specific data as to the prior invention of the species Compound VII of Stetter. Could he, this case would be governed by In re Stempel, 241 F.2d 755, 44 CCPA 820, holding in a genus-species case that all the applicant can be required to show is priority with respect to so much of the claimed invention as the reference happens to show; when he has done that he has disposed of the reference.

[990] Because of its import, the body of the second affidavit is reproduced in full:

I, ROBERT L. CLARKE, being duly sworn, depose and say that:
I am the Robert L. Clarke who is the applicant in the above-identified application and who executed on April 30, 1962 the Antedating Affidavit submitted with the response filed May 1,1962 in the above-identified application;
In the United States of America prior to September 15, 1958, I conceived the broad idea of the generic invention described in the above-identified application and embodied in Claims 1 and 2 thereof and I carried out the preparation of and had testing done on exemplary compounds as described in said antedating affidavit for the purpose of verifying the operability of said broad idea of the generic invention and I concluded from said preparation and testing of the exemplary compounds that the broad idea of the generic invention was operative as I conceived it;
And further I say not.

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Application of Robert L. Clarke, 356 F.2d 987, 53 C.C.P.A. 954 (ccpa 1966).

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