Prosecution Insights
Last updated: May 29, 2026
Application No. 17/627,221

HERBICIDAL COMPOSITION CONTAINING R-TYPE PYRIDYLOXY CARBOXYLIC ACID DERIVATIVE AND USE THEREOF

Non-Final OA §103§112
Filed
Jan 14, 2022
Priority
Jul 27, 2019 — CN 201910685431.9 +5 more
Examiner
PALLAY, MICHAEL B
Art Unit
1617
Tech Center
1600 — Biotechnology & Organic Chemistry
Assignee
Qingdao Kingagroot Chemical Compound Co. Ltd.
OA Round
4 (Non-Final)
56%
Grant Probability
Moderate
4-5
OA Rounds
0m
Est. Remaining
91%
With Interview

Examiner Intelligence

Grants 56% of resolved cases
56%
Career Allowance Rate
398 granted / 713 resolved
-4.2% vs TC avg
Strong +35% interview lift
Without
With
+34.8%
Interview Lift
resolved cases with interview
Typical timeline
3y 2m
Avg Prosecution
40 currently pending
Career history
770
Total Applications
across all art units

Statute-Specific Performance

§101
0.8%
-39.2% vs TC avg
§103
67.8%
+27.8% vs TC avg
§102
6.2%
-33.8% vs TC avg
§112
4.5%
-35.5% vs TC avg
Black line = Tech Center average estimate • Based on career data from 713 resolved cases

Office Action

§103 §112
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 . Status Applicant’s response dated 21 January 2026 to the previous Office action dated 21 October 2025 is acknowledged. Pursuant to amendments therein, claims 3, 5-8, 10, and 13-21 are pending in the application. A new rejection under 35 U.S.C. 112 is made herein in view of applicant’s claim amendments. The rejection under 35 U.S.C. 103 made in the previous Office action is withdrawn in view of applicant’s claim amendments, but a new (modified) rejection under 35 U.S.C. 103 is made herein in view of applicant’s claim amendments. Election/Restrictions Claims 10 and 17-21 are withdrawn from further consideration pursuant to 37 CFR 1.142(b), as being drawn to a nonelected invention, there being no allowable generic or linking claim. Applicant timely traversed the restriction (election) requirement in the reply filed on 24 September 2024. Applicant’s election of Compound A2 as species of active ingredient A in the reply filed on 24 September 2024 is acknowledged. Because applicant did not distinctly and specifically point out the supposed errors in the restriction requirement, the species election has been treated as an election without traverse (MPEP § 818.01(a)). Active ingredient A species other than Compound A2 are withdrawn from further consideration pursuant to 37 CFR 1.142(b) as being drawn to nonelected species. Election was made without traverse in the reply filed on 24 September 2024. Applicant’s election of glufosinate ammonium as species of active ingredient B in the reply filed on 24 September 2024 is acknowledged. Because applicant did not distinctly and specifically point out the supposed errors in the restriction requirement, the species election has been treated as an election without traverse (MPEP § 818.01(a)). Active ingredient B species other than glufosinate ammonium are withdrawn from further consideration pursuant to 37 CFR 1.142(b) as being drawn to nonelected species. Election was made without traverse in the reply filed on 24 September 2024. Claims 3, 5-8, and 13-16 are under current consideration. Claim Rejections - 35 USC § 112 The following is a quotation of 35 U.S.C. 112(b): (b) CONCLUSION.—The specification shall conclude with one or more claims particularly pointing out and distinctly claiming the subject matter which the inventor or a joint inventor regards as the invention. The following is a quotation of 35 U.S.C. 112 (pre-AIA ), second paragraph: The specification shall conclude with one or more claims particularly pointing out and distinctly claiming the subject matter which the applicant regards as his invention. Claim 13 is rejected under 35 U.S.C. 112(b) or 35 U.S.C. 112 (pre-AIA ), second paragraph, as being indefinite for failing to particularly point out and distinctly claim the subject matter which the inventor or a joint inventor (or for applications subject to pre-AIA 35 U.S.C. 112, the applicant), regards as the invention. Claim 13 depends upon claim 12, which has been canceled, and thus claim 13 is rejected as incomplete and therefore indefinite per MPEP 608.01(n)(V). Claim Rejections - 35 USC § 103 In the event the determination of the status of the application as subject to AIA 35 U.S.C. 102 and 103 (or as subject to pre-AIA 35 U.S.C. 102 and 103) is incorrect, any correction of the statutory basis (i.e., changing from AIA to pre-AIA ) for the rejection will not be considered a new ground of rejection if the prior art relied upon, and the rationale supporting the rejection, would be the same under either status. The following is a quotation of 35 U.S.C. 103 which forms the basis for all obviousness rejections set forth in this Office action: A patent for a claimed invention may not be obtained, notwithstanding that the claimed invention is not identically disclosed as set forth in section 102, if the differences between the claimed invention and the prior art are such that the claimed invention as a whole would have been obvious before the effective filing date of the claimed invention to a person having ordinary skill in the art to which the claimed invention pertains. Patentability shall not be negated by the manner in which the invention was made. This application currently names joint inventors. In considering patentability of the claims the examiner presumes that the subject matter of the various claims was commonly owned as of the effective filing date of the claimed invention(s) absent any evidence to the contrary. Applicant is advised of the obligation under 37 CFR 1.56 to point out the inventor and effective filing dates of each claim that was not commonly owned as of the effective filing date of the later invention in order for the examiner to consider the applicability of 35 U.S.C. 102(b)(2)(C) for any potential 35 U.S.C. 102(a)(2) prior art against the later invention. Claim(s) 3, 5-8, and 13-16 is/are rejected under 35 U.S.C. 103 as being unpatentable over Lian et al. ‘070 (CN 109535070 A; published 29 March 2019; of record; English machine translation made 28 December 2024; of record). Lian et al. ‘070 discloses an herbicidal composition comprising an herbicidally effective amount (claim 9 of translation) of a compound of formula I (claim 1 of translation) wherein additional herbicide can be mixed therewith (claim 8 of translation) such as glufosinate ammonium (pages 14-15 of translation) wherein the compound of formula I can be compound 68 (i.e., corresponds to instant compound A2) (pages of 21-22 and 25 of original document) wherein the active material or compound of formula I may be 0.1-99 wt% of the formulation (page 14 of translation) wherein the formulation may be dispersible oil suspension, water suspension, wettable powder, emulsifiable concentrate (page 13 of translation) wherein safener and/or auxiliary agents can be mixed therewith (claim 8 of translation) wherein mefenpyrdiethyl or furilazole can be mixed therewith (page 15 of translation) wherein surfactant can be mixed therein (page 13 of translation) wherein carrier can be mixed therein (page 14 of translation). It would have been prima facie obvious to a person of ordinary skill in the art before the effective filing date of the claimed invention to follow the suggestions of Lian et al. ‘070 as discussed above and to make the herbicidal composition thereof with an herbicidally effective amount of compound 68 (i.e., corresponds to instant compound A2) and glufosinate ammonium therein in amounts of 0.1-99 wt% of the formulation, and including safener, auxiliary agents, carrier, surfactant, mefenpyrdiethyl, and/or furilazole therein, wherein the formulation is a dispersible oil suspension, water suspension, wettable powder, or emulsifiable concentrate, with a reasonable expectation of success. Such active ingredient amounts of 0.1-99 wt% is presumed to be synergistic per MPEP 2112(V) and 2112.01(I) given that the composition of Lian et al. ‘070 is substantially identical to that of the claims, and given that compositions that are physically the same must have the same properties per MPEP 2112.01(II). Although Lian et al. ‘070 does not specifically disclose the R enantiomer/optical isomer form of compound 68, it would have been prima facie obvious to a person of ordinary skill in the art before the effective filing date of the claimed invention to make the herbicidal composition of Lian et al. ‘070 as discussed above wherein the compound 68 therein is the R enantiomer/optical isomer form (i.e., a type of stereoisomer) of compound 68, with a reasonable expectation of success, given that stereoisomers are prima facie obvious and stereoisomers are prima facie obvious over prior art mixtures of stereoisomers per MPEP 2144.09(II). Although Lian et al. ‘070 does not disclose such claimed weight ratios of ingredient A to ingredient B as set forth in claims 3 and 13, it would have been prima facie obvious to a person of ordinary skill in the art before the effective filing date of the claimed invention to optimize herbicidal effectiveness of the herbicidal composition of Lian et al. ‘070 as discussed above by varying the amounts of compound 68 (i.e., corresponds to instant compound A2) and glufosinate ammonium therein through routine experimentation per MPEP 2144.05(II), with a reasonable expectation of success, given that compound 68 (i.e., corresponds to instant compound A2) and glufosinate ammonium are both known herbicide active ingredients and thus both known result-effective variables, and also given that differences in concentration will generally not support patentability per MPEP 2144.05(II)(A). Regarding claims 5 and 14, the amount of 0.1-99 wt% active material as discussed above overlaps the claimed ranges of 1-95% and 10-80%, and a prima facie case of obviousness exists where prior art and claimed ranges overlap per MPEP 2144.05(I). Response to Declaration The declaration under 37 CFR 1.132 filed 21 January 2026 is insufficient to overcome the obviousness rejection as set forth in the last Office action because: although the declaration alleges unexpected results, it fails to clearly set forth the nature of the tested compositions (e.g., all components and concentrations thereof) such that it can be determined whether the asserted unexpected results are commensurate in scope with the claimed invention and whether the asserted unexpected results are truly unexpected. The burden is on applicant to establish that results are in fact unexpected and unobvious and of both statistical and practical significance, per MPEP 716.02(b). Such evidence of unexpected results must be commensurate in scope with the claimed invention per MPEP 716.02(d), and must compare the claimed subject matter with the closest prior art (or closer) per MPEP 716.02(e). At the very least, it is clear that the asserted unexpected results are limited to compound A2 as active ingredient A and glufosinate ammonium as active ingredient B, yet the claims are not limited as such nor are persuasive evidence and/or arguments presented indicating that such asserted unexpected results should be extended to encompass all claimed active ingredients A and B per MPEP 716.02(d)(I). Response to Arguments Applicant's arguments filed 21 January 2026 have been fully considered but they are not persuasive, in that they rely upon the declaration which is insufficient as discussed above. Conclusion No claims 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. Any inquiry concerning this communication or earlier communications from the examiner should be directed to MICHAEL B. PALLAY whose telephone number is (571)270-3473. The examiner can normally be reached Monday through Friday from 8:30 AM to 5:00 PM Eastern Time. 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, Sue Liu can be reached on (571)272-5539. 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. /MICHAEL B. PALLAY/Primary Examiner, Art Unit 1617
Read full office action

Prosecution Timeline

Show 5 earlier events
Sep 19, 2025
Request for Continued Examination
Sep 22, 2025
Response after Non-Final Action
Oct 21, 2025
Non-Final Rejection mailed — §103, §112
Jan 21, 2026
Response Filed
Jan 21, 2026
Response after Non-Final Action
Mar 09, 2026
Final Rejection mailed — §103, §112
May 06, 2026
Response after Non-Final Action
May 26, 2026
Interview Requested

Precedent Cases

Applications granted by this same examiner with similar technology

Patent 12611396
Microsphere-Based Injectible Celecoxib Formulation
4y 3m to grant Granted Apr 28, 2026
Patent 12610953
AGROCHEMICAL METHOD
2y 11m to grant Granted Apr 28, 2026
Patent 12605404
Synthetic Cellular Membrane Chemical Ionophore Delivery System Comprising Hexa-Aqua Ligand Compositions
4y 8m to grant Granted Apr 21, 2026
Patent 12604897
IMINODIPROPIONATE SURFACTANTS FOR AGRICULTURAL USE
4y 6m to grant Granted Apr 21, 2026
Patent 12605487
METAL SUBSTRATE WITH ANTIBACTERIAL AND OSTEOINTEGRATIVE PROPERTIES FOR IMPLANTOLOGY APPLICATIONS
4y 3m to grant Granted Apr 21, 2026
Study what changed to get past this examiner. Based on 5 most recent grants.

Strategy Recommendation AI-generated — please review before filing

Get a prosecution strategy drawn from examiner precedents, rejection analysis, and claim mapping.
Typically takes 5-10 seconds — AI-generated, attorney review required before filing

Prosecution Projections

4-5
Expected OA Rounds
56%
Grant Probability
91%
With Interview (+34.8%)
3y 2m (~0m remaining)
Median Time to Grant
High
PTA Risk
Based on 713 resolved cases by this examiner. Grant probability derived from career allowance rate.

Sign in with your work email

Enter your email to receive a magic link. No password needed.

Personal email addresses (Gmail, Yahoo, etc.) are not accepted.

Free tier: 3 strategy analyses per month