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公开(公告)号:US20240287005A1
公开(公告)日:2024-08-29
申请号:US18569408
申请日:2022-06-15
发明人: Pierre DUCRAY , Denise RAGEOT , Andreas TURBERG
IPC分类号: C07D261/04 , A01N43/80 , A01P7/02 , A01P7/04 , A61K31/42 , A61K31/422 , A61P33/14 , C07D413/12
CPC分类号: C07D261/04 , A01N43/80 , A01P7/02 , A01P7/04 , A61K31/42 , A61K31/422 , A61P33/14 , C07D413/12
摘要: The present invention provides compounds of formula (I):
which are useful for long-lasting treatment and control of pests, for example fleas and ticks, in companion animals and livestock, and pharmaceutical compositions and methods of using the same.-
公开(公告)号:US12065414B2
公开(公告)日:2024-08-20
申请号:US17465197
申请日:2021-09-02
发明人: Kumar Kamlesh Singh , Sanjay Jagdish Desai , Kuldeep Natwarlal Jain , Jitesh Amratlal Desai , Sarvil Dhirajbhai Patel
IPC分类号: C07D261/04
CPC分类号: C07D261/04
摘要: The invention relates to process for the preparation of isoxazoline-substituted benzamide compound and intermediates thereof. The invention also relates to process for the preparation of Fluralaner and intermediates thereof.
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公开(公告)号:US11858904B2
公开(公告)日:2024-01-02
申请号:US16761695
申请日:2018-11-06
申请人: Intervet Inc.
发明人: Luke Ryan Schenck , Athanas Koynov , George X. Zhou , Aaron Cote
IPC分类号: C07D261/04 , A01N43/80
CPC分类号: C07D261/04 , A01N43/80 , C07B2200/13
摘要: The application relates to a process to produce large isoxazoline compound particles which comprises initiating crystallization and then maintaining the temperature of the crystallization in the metastable region by removing, reheating and recycling a portion of the solvent thereby allowing the existing crystals to grow larger while minimizing the formation of newer smaller crystals.
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公开(公告)号:US11753385B2
公开(公告)日:2023-09-12
申请号:US17495481
申请日:2021-10-06
发明人: Teruhiko Ishikawa , Morita Iwami
IPC分类号: C07D211/44 , C07D211/46 , C07D211/74 , C07D261/04 , C07D498/04 , C07B33/00 , C07C225/06 , C07C271/18
CPC分类号: C07D261/04 , C07B33/00 , C07C225/06 , C07C271/18 , C07D211/44 , C07D211/46 , C07D211/74 , C07D498/04 , Y02P20/55
摘要: Provided is a production method of kakeromycin and a derivative thereof showing an antifungal activity and cytotoxicity and expected as a new antifungal agent or anticancer agent, by chemical synthesis. A production method of a compound represented by the formula (1):
wherein R is an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group; and n is 0 or 1, or a salt thereof, including a step of subjecting a compound represented by the formula (2):
wherein R and n are as defined above, or a salt thereof, to an oxidation reaction.-
公开(公告)号:US11753384B2
公开(公告)日:2023-09-12
申请号:US17049128
申请日:2019-04-24
发明人: Toshihiro Nagata , Daisuke Shikama
IPC分类号: C07D261/04 , B01J31/02
CPC分类号: C07D261/04 , B01J31/0232 , B01J31/0237 , B01J2231/348 , B01J2531/002
摘要: The objective of the present invention is to provide a production method for a 4,5-dihydroisoxazole represented by formula (3), which is safe, industrially desirable, economical, and environmentally friendly.
The present invention causes the compound of formula (1) to react with hydroxylamine in the presence of an acid catalyst to produce the compound of formula (3) through the reaction represented by the reaction equation.-
公开(公告)号:US20230174460A1
公开(公告)日:2023-06-08
申请号:US17920588
申请日:2021-04-21
发明人: Emily Balskus , Chi Le
IPC分类号: C07C229/42 , C07D261/04 , C07D239/34 , C07D241/18 , C07D239/42 , C07D237/14 , C07D231/56 , C07D213/65 , C07C229/36 , C07D213/64 , C07C291/04
CPC分类号: C07C229/42 , C07D261/04 , C07D239/34 , C07D241/18 , C07D239/42 , C07D237/14 , C07D231/56 , C07D213/65 , C07C229/36 , C07D213/64 , C07C291/04
摘要: The present disclosure provides compounds of formula (I), (II), and (Ia):
Methods of preparing these molecules and their use for treatment of Parkinson's Disease are described.-
公开(公告)号:US11649219B2
公开(公告)日:2023-05-16
申请号:US16406768
申请日:2019-05-08
IPC分类号: C07D261/04 , A01N43/80
CPC分类号: C07D261/04 , A01N43/80 , C07B2200/13 , A01N43/80 , A01N25/12
摘要: A process for preparing clomazone is provided, the process comprising reacting 4,4-dimethyl-3-isoxazolidinone with 2-chlorobenzyl chloride in an aqueous medium in the presence of a base, in particular an alkali metal hydroxide. A method for preparing clomazone is also disclosed, the method comprising (a) crystallizing clomazone from solution in an organic solvent; and (b) isolating the resulting crystals. N-benzene is a particularly suitable solvent. Further, there is provided Form I crystalline 2-[(2-chlorophenyl)methyl]-4,4-dimethyl-3-isoxazolidinone (clomazone), wherein the polymorph Form I is characterized by at least one of the following properties:
(i) an X-ray powder diffraction pattern having characteristic peaks expressed in degrees 2θ(+/−0.20° θ) at one or more of the following positions: about 10.63, 16.07, 18.08, 19.11, 19.34, 21.20, 24.78 and 28.80; and
(ii) an infrared (IR) spectrum having a characteristic peak: at about 2967 and 2870 cm−1.-
公开(公告)号:US11576382B2
公开(公告)日:2023-02-14
申请号:US16968913
申请日:2019-02-01
申请人: FMC Corporation
发明人: Ming Xu , George Philip Lahm , Jeffrey Keith Long
IPC分类号: A01N43/80 , C07D261/04 , C07D413/12
摘要: Disclosed are compounds of Formula 1, wherein J is and R1a, R1b, R2, R3, R4, R5, R6, R7, R8, R14, R15, R16, Q and X are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula 1 and methods for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound or a composition of the invention.
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公开(公告)号:US11324220B2
公开(公告)日:2022-05-10
申请号:US16928493
申请日:2020-07-14
发明人: Chunhua Yang
IPC分类号: C07D453/04 , C07D261/04 , A01N43/80 , A01N43/42 , A61K31/42
摘要: This invention relates to processes for the preparation of antiparasitic isoxazoline compounds enriched in an enantiomer using quinine-based chiral phase transfer catalyst. The invention also relates to novel quinine-based phase transfer catalysts and to a toluene solvent form of the isoxazoline compound of the invention.
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公开(公告)号:US20220073479A1
公开(公告)日:2022-03-10
申请号:US17414477
申请日:2019-12-20
申请人: Intervet Inc.
发明人: Harald Schmitt
IPC分类号: C07D261/04
摘要: The present invention relates to a novel method for preparing (5S)-4-[5-(3,5-di-chlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]-2-methyl-benzoic acid, which can preferably be used in the synthesis of (5S)-4-[5-(3,5-dichlorophenyl)-5-(trifluoro-Q methyl)-4H-isoxazol-3-yl]-N-[2-oxo-2-(2,2,2-trifluoroethylamino)ethyl]-2-methyl-benzamide.
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