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公开(公告)号:US10526264B2
公开(公告)日:2020-01-07
申请号:US16315417
申请日:2017-06-23
Applicant: BASF SE
Inventor: Martin John McLaughlin , Karsten Koerber , Birgit Gockel , Pascal Bindschaedler , Sebastian Soergel , Devendra Vyas , Johannes Roeckl
IPC: C07C33/00 , C07C17/00 , C07C25/00 , C07C45/00 , C07C63/00 , C07C33/48 , C07C49/813 , C07C45/51 , C07C63/74 , C07C17/263 , C07C25/24
Abstract: Compounds of formula I a process for preparation of compounds of formula I; precursor compounds of formula II a process for preparation of precursor compounds of formula II; compounds of formula III a process for the preparation of compounds of formula IV from compounds of formula III and the use of compounds of formula I for the preparation of compounds of formula IV.
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公开(公告)号:US20230322693A1
公开(公告)日:2023-10-12
申请号:US18028129
申请日:2021-09-28
Applicant: BASF SE
Inventor: Christopher Koradin , Harish Shinde , Martin John McLaughlin , Rahul Kaduskar , Philipp M. Staehle , Roland Goetz , Sunil Khamkar
IPC: C07D277/56
CPC classification number: C07D277/56
Abstract: The present invention relates to a process for the preparation 2-chloro-1-(2-chlorothiazol-5-yl)ethanone.
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公开(公告)号:US10961213B2
公开(公告)日:2021-03-30
申请号:US16480407
申请日:2018-01-16
Applicant: BASF SE
Inventor: Martin John McLaughlin , Karsten Koerber , Birgit Gockel , Devendra Vyas , Arun Narine
IPC: C07D307/79
Abstract: The present invention relates to a process for preparing benzylic amides of formula I wherein the variables have the meaning as defined in the description, by reductive amidation of a nitrile of formula II wherein the variables have the meanings given for formula I, with an activated carbonyl compound of formula III, and which nitrile is obtained by reaction of a compound of formula IV with a halogen compound of formula V, wherein X is a halogen atom, preferably bromo, which halogen compound V in turn is obtained by Sandmeyer reaction of an aniline derivative of formula VI novel compounds of formula I, and processes for preparing compounds of formula XII wherein the variables have the meaning as defined in the description by condensing compounds of formula I with compounds of formula X and subjecting the resulting α,β-unsaturated ketone of formula XI to a reaction with hydroxylamine to yield compounds of formula XII.
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公开(公告)号:US20180297979A1
公开(公告)日:2018-10-18
申请号:US15764414
申请日:2016-09-29
Applicant: BASF SE
Inventor: Martin John McLaughlin , Karsten Koerber , Birgit Gockel , Wolfgang von Deyn
IPC: C07D401/06 , A01N43/54 , A01N25/02 , A01N25/08
Abstract: Provided herein are imino compounds of formula I and stereoisomers, tautomers and salts thereof. Further provided herein are agricultural and veterinary compositions including the compounds. Also provided herein are methods related to the use of these compounds, and the stereoisomers, tautomers and/or salts thereof, for combating invertebrate pests. Further provided herein are methods for combating invertebrate pests, wherein the methods include applying such compounds, steroisomers, tautomers, and salts.
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公开(公告)号:US20240101547A1
公开(公告)日:2024-03-28
申请号:US18272840
申请日:2022-01-21
Applicant: BASF SE
Inventor: Christopher Koradin , Martin John McLaughlin , Roland Goetz , Rahul Kaduskar , Harish Shinde , Guillaume Michel Jacques Garivet
IPC: C07D417/12
CPC classification number: C07D417/12
Abstract: The present invention relates to a method for preparing 2-[2-(2-chlorothiazol-5-yl)-2-oxo-ethyl]sulfanyl-6-hydroxy-3-methyl-5-phenyl-pyrimidin-4-one or a tautomer thereof, to 2-[2-(2-chlorothiazol-5-yl)-2-oxo-ethyl]sulfanyl-6-hydroxy-3-methyl-5-phenyl-pyrimidin-4-one or a tautomer thereof and to its use as intermediate in the preparation of 2,3-dihydrotheiazolo [3,2-a]pyrimidinium compounds, and specifically of 3-(2-chlorothiazol-5-yl)-8-methyl-7-oxo-6-phenyl-2,3-dihydrothiazolo [3,2-a]pyrimidin-4-ium-5-olate and enantiomerically enriched forms thereof.
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公开(公告)号:US20220017439A1
公开(公告)日:2022-01-20
申请号:US17295102
申请日:2019-11-25
Applicant: BASF SE
Inventor: Karsten Koerber , Michael Rack , Pascal Bindschaedler , Martin John McLaughlin , Birgit Gockel , Devendra Vyas , Sebastian Soergel
Abstract: The invention relates to a process for the preparation of 5-bromo-1,3-dichloro-2-fluoro-benzene by diazotization and reduction of 6-bromo-2,4-dichloro-3-fluoro-aniline, which is obtained by bromination of 2,4-dichloro-3-fluoro-aniline, which is obtained by reduction of 1,3-dichloro-2-fluoro-4-nitro-benzene, and a process for preparing active compounds of formula V (Formula V) wherein the variables are defined in the specification by further transforming 5-bromo-1,3-dichloro-2-fluoro-benzene obtained from 2,4-dichloro-3-fluoro-aniline by the process according to the invention.
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公开(公告)号:US20210380569A1
公开(公告)日:2021-12-09
申请号:US17288976
申请日:2019-10-28
Applicant: BASF SE
Inventor: Roland Goetz , Michael Rack , Martin John McLaughlin , Harish Shinde , Ritesh Karalkar , Kailaskumar Borate , Karsten Koerber , Arun Narine , Nikolas Huwyler
IPC: C07D413/04 , B01J31/02
Abstract: The invention relates to a process for preparing optically enriched isoxazoline compounds of formula (I), wherein the variables are as defined in the specification, and the shown enantiomer has at least 80% ee; by oxo-Michael addition of hydroxyl amine or its salt to an enone of formula (II), wherein the variables have the meanings given for formula (I), in the presence of a catalyst of formula (III) and a base.
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公开(公告)号:US10206397B2
公开(公告)日:2019-02-19
申请号:US15023128
申请日:2014-09-18
Applicant: BASF SE
Inventor: Martin John McLaughlin , Nina Gertrud Bandur , Matthias Pohlman , Jochen Dietz , Wolfgang Von Deyn
IPC: A01N43/40 , C07D405/14 , C07D401/06 , C07D405/06 , C07D417/06 , A01N43/54 , A01N43/78 , A01N53/00 , C07D401/14 , C07D417/14
Abstract: The present invention relates to N-acylimino compound of formula (I): wherein X is O or S, in particular O; m is an integer selected from 0, 1, 2, 3, 4, 5 or 6; Het is a 5 or 6 membered carbon-bound or nitrogen-bound heterocyclic ring, W1-W2-W3-W4 represents a carbon chain group connected to N and C═N, and thus forming a saturated, unsaturated, or partially unsaturated 5 or 6 membered nitrogen containing heterocycle, wherein W1, W2, W3 and W4 each individually represent CRvRw, R1, R2 may be hydrogen, halogen, etc. R3 may be hydrogen, halogen, CN, C1-C6-alkyl, etc. R4a, R4b if present, may be hydrogen, halogen, C1-C6-alkyl, etc. R5 may be hydrogen, halogen, C1-C6-alkyl, C1-C6-alkenyl, C1-C6-alkinyl, C3-C8-cycloalkyl, S(O)nNR9aR9b, NR9aR9b, C(═O)OR8, C(═O)NR9aR9b, C(═S)NR9aR9b, C(═O)R7a, C(═S)R7a, NR9a—C(═O)R7a, NR9a—C(═S)R7a, NR9a—S(O)nR8a, a moiety Q-phenyl, where the phenyl ring is optionally substituted with one or more, e.g. 1, 2, 3, 4 or 5 identical or different substituents R10, or a moiety Q-Het#, or R3 and R5 together may also form with the carbon atom they are bound to, a 3, 4, 5 or 6 membered saturated partially unsaturated carbocycle or heterocycle. The invention also relates to the use of the N-acylimino heterocyclic compounds, their stereoisomers, their tautomers and their salts, for combating invertebrate pests. Furthermore the invention relates also to methods of combating invertebrate pests, which comprises applying such compounds.
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公开(公告)号:US20240101575A1
公开(公告)日:2024-03-28
申请号:US18272820
申请日:2022-01-21
Applicant: BASF SE
Inventor: Christopher Koradin , Martin John McLaughlin , Roland Goetz , Rahul Kaduskar , Harish Shinde
IPC: C07D513/04
CPC classification number: C07D513/04
Abstract: The present invention relates to a method for preparing an enantiomerically enriched form of 3-(2-chlorothiazol-5-yl)-8-methyl-7-oxo-6-phenyl-2,3-dihydrothiazolo[3,2-a]pyrimidin-4-ium-5-olate.
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公开(公告)号:US11440861B2
公开(公告)日:2022-09-13
申请号:US17295102
申请日:2019-11-25
Applicant: BASF SE
Inventor: Karsten Koerber , Michael Rack , Pascal Bindschaedler , Martin John McLaughlin , Birgit Gockel , Devendra Vyas , Sebastian Soergel
IPC: C07C17/35 , B01J21/18 , B01J23/44 , C07C25/08 , C07C245/20 , C07C37/045 , C07C39/30 , C07C17/093
Abstract: The invention relates to a process for the preparation of 5-bromo-1,3-dichloro-2-fluoro-benzene by diazotization and reduction of 6-bromo-2,4-dichloro-3-fluoro-aniline, which is obtained by bromination of 2,4-dichloro-3-fluoro-aniline, which is obtained by reduction of 1,3-dichloro-2-fluoro-4-nitro-benzene, and a process for preparing active compounds of formula V (Formula V) wherein the variables are defined in the specification by further transforming 5-bromo-1,3-dichloro-2-fluoro-benzene obtained from 2,4-dichloro-3-fluoro-aniline by the process according to the invention.
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