BY-LAW 639-05 PDF

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Quite clearly, the very reference relied on by the examiner teaches that compounds similar in structure in this art do not possess similar properties. We disagree with the examiner’s position.

R1 represents hydrogen, lower alkyl, cycloalkyl-lower alkyl of not more than 10 carbon atoms, lower alkenyl, lower alkynyl, di-lower alkylamino -lower alkyl, hydroxy lower alkyl, alkoxy lower alkyl, alkanoyloxy lower alkyl having 4 to 11 carbon atoms, lower alkylthio-lower alkyl, phenyl-lower alkyl, phenyl- lower alkyl substituted by halogen with an atomic number up to 35, lower alkyl, lower alkoxy, methylenedioxy, and trifluoromethyl, or lower alkanoyl, the ring A is unsubstituted or substituted by halogen with an atomic number up to 35, lower alkyl, hydroxyl, lower alkoxy, alkanoyloxy having carbon atoms, lower alkylthio, trifluoromethyl or cyano, X represents 0, S, methylene, a direct bond or a divalent radical of the partial formula.

A method of treating states of agitation in a warmblooded animal which comprises administering to said animal a therapeutically effective amount of a compound according to claim 17, or a pharmaceutically acceptable acid addition salt thereof. The sole issue presented for review is whether the examiner correctly rejected claims 6, 7, 9 and 11 through 20 under 35 U.

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In obviousness rejections based on close similarity in chemical structure, the prima facie case of obviousness rises from the expectation that compounds similar in structure will have similar properties. The single prior art reference relied on by the examiner is: Pyrrolidino and piperidino compounds contain a 5- and 6-membered ring, respectively.

Claims 17, 11 and 14 are representative. In the examiner’s answer, page 2, the examiner indicates that the subject matter defined in claims 8 and 10 is allowable over the prior art of record. As described therein, the pyrrolidino derivatives are useful in treating conditions of stress and agitation whereas the piperidino compounds are useful in treating depressed patients.

We agree with appellants that a person having 639-0 skill in the art, given only the van der Burg patent but not appellants’ disclosure, would not have had sufficient basis to predict what, if any, utility appellants’ azepine compounds might possess. The examiner here takes the position that appellants’ claimed compounds, pharmaceutical compositions containing same, and method of treating states of agitation by administering same would have been obvious in view of the disclosure of van der Burg.

See the van der Burg patent, column 1, lines 43 through As acknowledged by the examiner in his answer, page 4, a person having ordinary skill in the art ‘knows that the 5- and 6-membered compounds also possess opposite utilities. This leaves for our review claims 6, 7, 9 and 11 through A compound which is neither because the depressant and anti-depressant effects counteract each other?

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Accordingly, the examiner’s decision is reversed. Specifically, the examiner asserts that appellants’ azepine compounds which contain a 7-membered ring would have been prima facie obvious in view of the closely related pyrrolidino and piperidino compounds disclosed by the prior art reference.

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The very prior art reference here relied on by by-lae examiner, however, undermines the prima facie case because the reference teaches that compounds similar in structure in this art do not possess similar properties. Skip to main content.

In conclusion the examiner’s prima facie case of obviousness is based on the expectation that compounds which are similar in structure will have similar properties. Application for Patent filed September 29,Serial No.

More specifically, the issue is whether the examiner has established that the claimed subject matter would have been prima facie obvious in view of the disclosure of van der Burg. A pharmaceutical composition useful in the treatment of states of agitation in a warmblooded animal comprising a therapeutically effective amount of an azatetracyclic compound according to claim 17, or a pharmaceutically acceptable acid addition salt bg-law together with a pharmaceutical carrier.

This fact is not in dispute. Van der Burg discloses that the known pyrrolidino and piperidino compounds possess diametrically opposite utilities.

O. Reg. 639/05: Conditions of Carriage – Household Goods Carriers

This appeal arises from the examiner’s final rejection of claims 6 through 20, which are all of the claims in the application. In re Payne, F.

What utility would a person having ordinary skill in the art have expected for the azepine or 7-membered ring compound?