Prosecution Insights
Last updated: May 04, 2026
Application No. 17/912,418

SYNTHESIS OF 3'N NUCLEOSIDES THROUGH OXIME INTERMEDIATES AND RELATED COMPOUNDS

Final Rejection §102
Filed
Sep 16, 2022
Priority
Mar 16, 2020 — provisional 62/990,361 +1 more
Examiner
LEWIS, PATRICK T
Art Unit
1691
Tech Center
1600 — Biotechnology & Organic Chemistry
Assignee
Janssen Biopharma Inc.
OA Round
2 (Final)
74%
Grant Probability
Favorable
3-4
OA Rounds
0m
Est. Remaining
89%
With Interview

Examiner Intelligence

Grants 74% — above average
74%
Career Allowance Rate
848 granted / 1140 resolved
+14.4% vs TC avg
Moderate +14% lift
Without
With
+14.3%
Interview Lift
resolved cases with interview
Typical timeline
2y 3m
Avg Prosecution
35 currently pending
Career history
1175
Total Applications
across all art units

Statute-Specific Performance

§101
4.0%
-36.0% vs TC avg
§103
30.5%
-9.5% vs TC avg
§102
20.4%
-19.6% vs TC avg
§112
21.4%
-18.6% vs TC avg
Black line = Tech Center average estimate • Based on career data from 1140 resolved cases

Office Action

§102
DETAILED ACTION Notice of Pre-AIA or AIA Status The present application, filed on or after March 16, 2013, is being examined under the first inventor to file provisions of the AIA . Applicant’s Response Dated September 17, 2025 In the Response dated September 17, 2025, claims 1, 4, 6-7, 22-24, 26, and 29-30 were amended, and claim 32 was canceled. Claims 1-2, 4, 6-8, 10-13, 17-19, 22-24, 26, and 29-30 are pending. An action on the merits of claims 1-2, 4, 6-8, 10-13, 17-19, 22-24, 26, and 29-30 is contained herein. The rejection of claims 1, 6-8, 10-13, and 29-30 under 35 U.S.C. 102(a)(1) as being anticipated by Kojima, Naoshi, Istvan E. Szabo, and Thomas C. Bruice. "Synthesis of ribonucleic guanidine: replacement of the negative phosphodiester linkages of RNA with positive guanidinium linkages." Tetrahedron 58.5 (2002): 867-879 (Kojima) has been rendered moot in view of applicant’s amendment dated September 17, 2025. The rejection of claims 1, 6-8, and 10-13 under 35 U.S.C. 102(a)(1) as being anticipated by Ogawa, Akira, et al. "Nucleosides and Nucleotides. 180. Synthesis and Antitumor Activity of Nucleosides That Have a Hydroxylamino Group Instead of a Hydroxyl Group at the 2 ‘-or 3 ‘-Position of the Sugar Moiety." Journal of medicinal chemistry 41.25 (1998): 5094-5107 (Ogawa) has been rendered moot in view of applicant’s amendment dated September 17, 2025. The rejection of claim 23 under 35 U.S.C. 102(a)(1) as being anticipated by Khalil et al. Eur. J. Org. Chem. 2012, 3172–3179 (Khalil) is maintained. The rejection of claims 24 and 26 under 35 U.S.C. 102(a)(1) as being anticipated by Khalil et al. Eur. J. Org. Chem. 2012, 3172–3179 (Khalil) has been rendered moot in view of applicant’s amendment dated September 17, 2025. The rejection of claim 18 under 35 U.S.C. 103 as being unpatentable over Kojima, Naoshi, Istvan E. Szabo, and Thomas C. Bruice. "Synthesis of ribonucleic guanidine: replacement of the negative phosphodiester linkages of RNA with positive guanidinium linkages." Tetrahedron 58.5 (2002): 867-879 (Kojima) has been rendered moot in view of applicant’s amendment dated September 17, 2025. Rejections Set Forth in the Office Action Dated May 23, 2025 The text of those sections of Title 35, U.S. Code not included in this action can be found in a prior Office action. Claim(s) 23 is/are rejected under 35 U.S.C. 102(a)(1) as being anticipated by Khalil et al. Eur. J. Org. Chem. 2012, 3172–3179 (Khalil). Applicant's arguments filed September 17, 2025 have been fully considered but they are not persuasive. Applicant submits that Khalil fails to teach or disclose a nucleoside of Formula (I') or (II') having a nucleobase selected from the group consisting of adenine, adenine comprising an N-benzoyl protecting group, adenine comprising an N-benzyl protecting group, guanine comprising an N- benzoyl protecting group, guanine comprising an N-isobutyryl group, uracil, and thymine, as recited in claim 23. Applicant submits, each of compounds 18 and 19 of Khalil has a cytosine nucleobase, and these compounds are thereby outside the scope of B of Formula (I') or (II') of claim 23 since B cannot be cytosine. Applicant’s amendment and argument has been fully considered; however, Khalil further teaches compounds 7 and 9 (Figure 2). Compound 7 or 9 is embraced by instant formula (I’) or formula (II’), respectively, wherein B = uracil; R = H; and R2 = F. Thus, the rejection is maintained. Conclusion Claims 1-2, 4, 6-8, 10-13, 17-19, 22-24, 26, and 29-30 are pending. Claim 23 is rejected. Claims 24 and 26 are objected to as being dependent upon a rejected base claim, but would be allowable if rewritten in independent form including all of the limitations of the base claim and any intervening claims. Claims 1-2, 4, 6-8, 10-13, 17-19, 22, and 29-30 are allowed. Applicant's amendment necessitated the new ground(s) of rejection presented in this Office action. Accordingly, THIS ACTION IS MADE FINAL. See MPEP § 706.07(a). Applicant is reminded of the extension of time policy as set forth in 37 CFR 1.136(a). A shortened statutory period for reply to this final action is set to expire THREE MONTHS from the mailing date of this action. In the event a first reply is filed within TWO MONTHS of the mailing date of this final action and the advisory action is not mailed until after the end of the THREE-MONTH shortened statutory period, then the shortened statutory period will expire on the date the advisory action is mailed, and any nonprovisional extension fee (37 CFR 1.17(a)) pursuant to 37 CFR 1.136(a) will be calculated from the mailing date of the advisory action. In no event, however, will the statutory period for reply expire later than SIX MONTHS from the mailing date of this final action. Contacts Any inquiry concerning this communication or earlier communications from the examiner should be directed to PATRICK T LEWIS whose telephone number is (571)272-0655. The examiner can normally be reached Monday to Friday, 10 AM to 4 PM EST (Maxi Flex). Examiner interviews are available via telephone, in-person, and video conferencing using a USPTO supplied web-based collaboration tool. To schedule an interview, applicant is encouraged to use the USPTO Automated Interview Request (AIR) at http://www.uspto.gov/interviewpractice. If attempts to reach the examiner by telephone are unsuccessful, the examiner’s supervisor, Deirdre Claytor can be reached at (571) 272-8394. The fax phone number for the organization where this application or proceeding is assigned is 571-273-8300. Information regarding the status of published or unpublished applications may be obtained from Patent Center. Unpublished application information in Patent Center is available to registered users. To file and manage patent submissions in Patent Center, visit: https://patentcenter.uspto.gov. Visit https://www.uspto.gov/patents/apply/patent-center for more information about Patent Center and https://www.uspto.gov/patents/docx for information about filing in DOCX format. For additional questions, contact the Electronic Business Center (EBC) at 866-217-9197 (toll-free). If you would like assistance from a USPTO Customer Service Representative, call 800-786-9199 (IN USA OR CANADA) or 571-272-1000. /PATRICK T LEWIS/Primary Examiner, Art Unit 1691 /PL/
Read full office action

Prosecution Timeline

Sep 16, 2022
Application Filed
May 21, 2025
Non-Final Rejection — §102
Sep 17, 2025
Response Filed
Jan 07, 2026
Final Rejection — §102
Apr 06, 2026
Request for Continued Examination
Apr 07, 2026
Response after Non-Final Action

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Study what changed to get past this examiner. Based on 5 most recent grants.

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Prosecution Projections

3-4
Expected OA Rounds
74%
Grant Probability
89%
With Interview (+14.3%)
2y 3m (~0m remaining)
Median Time to Grant
Moderate
PTA Risk
Based on 1140 resolved cases by this examiner. Grant probability derived from career allowance rate.

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