Application of Herman Hoeksema

379 F.2d 1007, 54 C.C.P.A. 1618
CourtCourt of Customs and Patent Appeals
DecidedJune 29, 1967
DocketPatent Appeal 7778
StatusPublished
Cited by4 cases

This text of 379 F.2d 1007 (Application of Herman Hoeksema) is published on Counsel Stack Legal Research, covering Court of Customs and Patent Appeals primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Application of Herman Hoeksema, 379 F.2d 1007, 54 C.C.P.A. 1618 (ccpa 1967).

Opinion

KIRKPATRICK, Judge.

This appeal is from a decision of the Board of Appeals affirming the examiner’s rejection of claim 1 in appellant’s application serial No. 30,770, filed May 23, 1960, for “9-D-Psicofuranosylpurine and 6-Substituted Derivatives.” Claims 2 and 11-25 were allowed.

The subject matter is best illustrated by the appealed claim which reads: 1

1. An N-psieofuranoside having the formula:

wherein A is selected from the class consisting of hydrogen, the group -XR wherein R is selected from the class consisting of hydrogen, lower-alkyl, and lower-aralkyl, and X is selected from the class consisting of oxygen R2 and sulfur, and the group -NC^' ^^Rs wherein R2 is selected from the class consisting of hydrogen, lower-alkyl, lower-aralkyl, and lower-aryl, and R3 is selected from the class consisting of lower-alkyl, lower-aralkyl, and lower-aryl, and R' is selected from the class consisting of hydrogen, a hydrocarbon carboxylic acid acyl radical containing from two to twelve carbon atoms, inclusive, and a halo-, hydroxy-, lower-alkoxy-, amino-, cyano-, thioeyano-, and nitro-substituted hydrocarbon carboxylic acid acyl radical containing from two to twelve carbon atoms, inclusive.

The compounds embraced in the appealed claim are derivatives of a purine having a D-psicofuranosyl group attached to the 9-position of the purine. The controversy here is limited to the substituent A at the 6-position of the purine ring system. As the appealed claim states, A may represent the group -NR2R3 wherein R2 may be a hydrogen, lower alkyl, lower aralkyl or lower aryl, and R3 may be lower alkyl, lower aralkyl and lower aryl. Thus, the substituent A may be a secondary or tertiary amino group but it may not be a primary or unsubstituted amino group. The allowed claims all relate to products and processes where A is not an amino group.

The reference relied on is: 2

De Boer et al. 3,094,460 June 18, 1963 (filed January 20, 1959)

In the disclosure of De Boer et al., there is disclosed a new antibiotic material called psicofuranine which has the following structural formula:

*1009 It is clear that the appealed claim is readable on psicofuranine except for the substituent on the number 6-carbon in the purine ring system: Psicofuranine has a primary amino group whereas the claimed N-psicofuranoside has a substituted amino group at that position.

Recognizing the close resemblance of the reference compound to a compound within the scope of the appealed claim, appellant argued that his 6-lower-alkyl-amino -9 - D - psicofuranosylpurine and 6 - di - lower-alkylamino - 9 - D -psicofur-anosylpurine encompassed by the appealed claim are not obvious to one of ordinary skill in the art because De Boer et al. do not teach a method for producing appellant’s compounds and because there is no known or obvious method for producing them. Appellant contended that one of ordinary skill in the art would not know how to produce the claimed compounds with the disclosure of the De Boer et al. patent and, therefore, that that patent does not place appellant’s compounds in the possession of the public. In re Brown, 329 F.2d 1006, 51 CCPA 1254. In addition, appellant submitted an affidavit by one Dr. Paul F. Wiley who stated: that he does not believe the fermentation process disclosed in De Boer et al. could be adapted to the production of the instant claimed compounds; that the 6-amino-9-D-psicofur-anosylpurine of De Boer et al. could not be transformed by direct chemical substitution of the 6-amino group to the presently claimed compounds; and that such transformations could be carried out only by a complex multi-step procedure such as that described in the application on appeal.

The examiner rejected the appealed claim as being obvious in view of the disclosure of De Boer et al. under 35 U.S.C. § 103. It was the examiner’s position that the psicofuranine of De Boer et al. is the next lower homolog of a specific compound within the scope of the appealed claim: namely, where A is -NH-lower alkyl. The examiner further was of the opinion that appellant’s claimed 6-lower-alkylamino compound is so closely related to the 6-amino homolog of De Boer et al. as to be obvious to a chemist of ordinary skill and thus prima facie unpatentable thereover. With respect to the Wiley affidavit, the examiner commented that it is directed to the processes for preparing various compounds and it shows nothing unobvious for the claimed compounds. The examiner also gave little weight to the affidavit since it is not supported by experimental data.

The board affirmed the decision of the examiner. Noting that the appellant’s position is that the reference is not an enabling disclosure and recognizing this court’s comment in In re Riden, 318 F.2d 761, 50 CCPA 1411, that “the method of making the compounds is a relevant fact to be considered in the question of obviousness of the compounds,” the board stated that in its opinion the method of making the compound should never be the overriding factor in determining the question of obviousness of the compound. The board further pointed to the fact that although appellant stated that his complex multi-step process is necessary to introduce the alkylamino substituent, he has not asserted it is the only method. Continuing, the board stated:

We believe any chemist of average competence would recognize that in a compound having several reactive groups, such as here involved, the direct approach is seldom feasible but that blocking of the various reactive groups ultimately to be retained is first necessary. This was also pointed out to appellant’s counsel at the oral hearing with specific reference to the practice in the synthesis of steroids. Therefore here, as in Riden et al. supra, there is no basis for definitely concluding that a chemist could not, within his skill, produce the compound in controversy.
Under the circumstances and on the basis of the record before us, we do not believe appellant should prevail solely on the asserted difficulty of making the claimed compounds or the fact that he has been allowed process claims *1010 for one method to that end. 3 [Emphasis and footnote ours.]

Before this court, appellant admits that his 6-lower-alkylamino compounds would not be patentable if an operable method for making them would have been obvious at the time the invention was made to one of ordinary skill in this art. Appellant has not submitted any showing of unexpected properties possessed by his compounds but he predicates patentability solely on the alleged unobviousness of the process for making the claimed compounds.

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Related

In re Coker
463 F.2d 1344 (Customs and Patent Appeals, 1972)
Application of Herman Hoeksema
399 F.2d 269 (Customs and Patent Appeals, 1968)

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Bluebook (online)
379 F.2d 1007, 54 C.C.P.A. 1618, Counsel Stack Legal Research, https://law.counselstack.com/opinion/application-of-herman-hoeksema-ccpa-1967.