Medichem, S.A. v. Rolabo, S.L., Defendant-Cross

353 F.3d 928, 69 U.S.P.Q. 2d (BNA) 1283, 2003 U.S. App. LEXIS 26236, 2003 WL 22999460
CourtCourt of Appeals for the Federal Circuit
DecidedDecember 23, 2003
Docket02-1461, 02-1480
StatusPublished
Cited by35 cases

This text of 353 F.3d 928 (Medichem, S.A. v. Rolabo, S.L., Defendant-Cross) is published on Counsel Stack Legal Research, covering Court of Appeals for the Federal Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Medichem, S.A. v. Rolabo, S.L., Defendant-Cross, 353 F.3d 928, 69 U.S.P.Q. 2d (BNA) 1283, 2003 U.S. App. LEXIS 26236, 2003 WL 22999460 (Fed. Cir. 2003).

Opinion

GAJARSA, Circuit Judge.

Medichem, S.A. (“Medichem”), appeals the decision of the United States District Court for the Southern. District of New York following a bench trial that there was no interference-in-fact under 35 U.S.C. *930 § 291 between the claimed inventions of U.S. Patent Nos. 6,084,100 (the “'100 patent”) belonging to Medichem and 6,093,827 (the “'827 patent”) belonging to Rolabo, S.L. (“Rolabo”). Medichem, S.A. v. Rolabo, S.L., No. 01-CV-3087 (S.D.N.Y. May 9, 2002) (“District Court Opinion”). Rolabo cross-appeals the district court’s conclusion that this was not an exceptional case under 35 U.S.C. § 285 and its denial of Rolabo’s request for attorney fees. Because we find the district court erred in its application of the two-way test, we vacate its priority determination, reverse its conclusion that the '827 patent was neither anticipated nor obvious in light of the '100 patent, and remand for further proceedings consistent with this opinion. As further proceedings are necessary, any resolution of Rolabo’s request for attorney fees under 35 U.S.C. § 285 is at this time premature.

I. BACKGROUND

A. The Patents

Medichem is a Barcelona-based manufacturer of pharmaceutical ingredients. The company is the assignee of the '100 patent, entitled “Process for the Preparation of Loratadine.” Loratadine is an antihistamine that is the active pharmaceutical ingredient in the popular allergy medication Claritin®. Rolabo is also a manufacturer of pharmaceutical ingredients based in Barcelona, Spain, and is the assignee of the '827 patent, entitled “Process for the Preparation of 10,ll-Dihydro-5H-diben-zoa[a,d] cyclohept-5-enes and Derivatives Thereof,” which, like the '100 patent, is a process for the preparation of Loratadine.

Claims 1 and 2 of the '100 patent claim read:

1. A process for the preparation of lor-atadine consisting of reacting, in an organic solvent and in the presence of a tertiary amine, 8-chloro-5,6-dihyrobenzo[5,6]cyclohepta[l,2-b]py-ridin-ll-one, of formula VII with a low-valent titanium species.
2. The process of claim 1, wherein the low-valent titanium species are generated by reduction of titanium tetrachloride with zinc dust.

'100 patent, col. 5, 1. 59 to col. 6, 1. 21. Claims 1 and 17 of the '827 patent read:

1. A process for preparing 5,6-dihy-dro-llH-dibenzo[a,d]cyclohept-ll-enes comprising reacting a diben-zosuberone or an aza derivative thereof with an aliphatic ketone in the presence of low-valent titanium wherein said low-valent titanium is generated by zinc.
17. A process as claimed in claim 1 for preparing Loratadine.

'827 patent, col. 5, 11. 34-38, col. 8, 11. 3-4 (emphasis added). Both the '100 and the '827 patents involve chemical reactions generally known in the art as “McMurry” reactions, after Professor John McMurry, who described the intermolecular coupling between the different carbonyl groups in a compound using low-valent titanium in a 1989 publication.

B. Proceedings to Date

1. District Court Proceedings

Medichem filed a complaint under 35 U.S.C. § 291 against Rolabo in the United States District Court for the Southern District of New York on April 13, 2001. Section 291, entitled “Interfering Patents,” provides a cause of action to one patent owner against another patent owner where the inventions claimed by their respective patents interfere with one another. Addressing priority first, the district court found that the evidence submitted by Med-ichem supported an invention date in the fall of 1996 for the '100 patent. Since Rolabo did not allege an invention date *931 prior to the fall of 1996, the district court awarded priority to Medichem.

The district court turned next to the issue of interference-in-fact between the '100 and '827 patents, and announced that it was applying the two-way test for identifying an interference provided in the Patent and Trademark Organization’s (“PTO”) regulation, 37 C.F.R. § 1.601(n). Under the two-way test, the district court first treated the '100 patent as prior art, identifying the key question as “whether the inclusion of tertiary amine in Medichem’s patent claims is material in a way that negates obviousness and makes the patents noninterfering.” 1 Because of the presence of a tertiary amine throughout the '100 patent’s claims and examples, the district court found that a tertiary amine would appear to a reader of the '100 patent as a necessary component of Medi-chem’s process. Absent the tertiary amine, the district court explained, it would not be obvious that the same result could be achieved. Therefore, the absence of a tertiary amine requirement in the '827 patent “strongly suggested]” that the two processes were materially different.

Continuing its analysis under the interference inquiry, the district court assessed whether one of ordinary skill in the art would find the elimination of a tertiary amine obvious or anticipated in light of the '100 patent and the prior art in 1996, the invention date of the '100 patent. The district court accepted each of the parties’ expert witnesses, five in all, as representative of the ordinary skill in the relevant art of synthetic organic chemistry. All witnesses were not, however, determined by the district court to be equally credible in their testimony. Ultimately, the 'district court relied entirely on the testimony of -Rolabo’s third expert, Dr. Leckta.

Dr; Leckta confirmed the district court’s belief that, while a person of skill in the ¿rt in 1996 would have understood the role of the tertiary amine in Medichem’s process, the result if the tertiary amine were omitted would not have been obvious. The tertiary amine, Dr. Leckta noted, was significant in aiding Medichem’s process for creating Loratadine, but also had drawbacks in the form of longer reaction times, lower yields, and additional workup time. Based on its conclusion that the removal of the tertiary amine would not be obvious to one of ordinary skill in the art in 1996, the district court found that one leg of the two-way test (i.e., treating the '100 patent as prior art) required by the PTO’s test for interferences under section 1.601(n) was not satisfied and, as a result, there could be no dnterference-in-fact. The district court .did not reach the second leg of the two-way test. Medichem timely appealed the - district court’s finding of no interference • and Rolabo cross-appealed the district court’s denial of attorney fees under § 285. We have jurisdiction pursuant to 28 U:S.C. § 1295(a)(1).

2. Interim PTO Proceedings

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353 F.3d 928, 69 U.S.P.Q. 2d (BNA) 1283, 2003 U.S. App. LEXIS 26236, 2003 WL 22999460, Counsel Stack Legal Research, https://law.counselstack.com/opinion/medichem-sa-v-rolabo-sl-defendant-cross-cafc-2003.