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EP4471004
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EP About this file: EP4471004
| EP4471004 - METHOD FOR PRODUCING AMIDE COMPOUND [Right-click to bookmark this link] | Status | Request for examination was made Status updated on 01.11.2024 Database last updated on 24.03.2026 | |
| Former | The international publication has been made Status updated on 05.08.2023 | Most recent event Tooltip | 17.12.2025 | New entry: Renewal fee paid | Applicant(s) | For all designated states Nippon Soda Co., Ltd. 2-7-2, Marunouchi Chiyoda-ku Tokyo 100-7010 / JP | [2024/49] | Inventor(s) | 01 /
NODA Kaoru Takaoka-shi, Toyama 933-8507 / JP | 02 /
TAKEHISA Katsuma Takaoka-shi, Toyama 933-8507 / JP | [2024/49] | Representative(s) | Mewburn Ellis LLP Aurora Building Counterslip Bristol BS1 6BX / GB | [2024/49] | Application number, filing date | 22924219.3 | 27.12.2022 | [2024/49] | WO2022JP48272 | Priority number, date | JP20220011981 | 28.01.2022 Original published format: JP 2022011981 | [2024/49] | Filing language | JA | Procedural language | EN | Publication | Type: | A1 Application with search report | No.: | WO2023145372 | Date: | 03.08.2023 | Language: | JA | [2023/31] | Type: | A1 Application with search report | No.: | EP4471004 | Date: | 04.12.2024 | Language: | EN | [2024/49] | Search report(s) | International search report - published on: | JP | 03.08.2023 | (Supplementary) European search report - dispatched on: | EP | 12.12.2025 | Classification | IPC: | C07C231/10, C07C237/06 | [2024/49] | CPC: |
C07C231/10 (EP,KR,US);
C07C237/06 (EP,KR);
Y02E60/10 (EP)
| C-Set: |
C07C231/10, C07C237/06 (EP)
| Designated contracting states | AL, AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LI, LT, LU, LV, MC, ME, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, TR [2024/49] | Title | German: | VERFAHREN ZUR HERSTELLUNG EINER AMIDVERBINDUNG | [2024/49] | English: | METHOD FOR PRODUCING AMIDE COMPOUND | [2024/49] | French: | PROCÉDÉ DE PRODUCTION D'UN COMPOSÉ AMIDE | [2024/49] | Entry into regional phase | 11.07.2024 | Translation filed | 11.07.2024 | National basic fee paid | 11.07.2024 | Search fee paid | 11.07.2024 | Designation fee(s) paid | 11.07.2024 | Examination fee paid | Examination procedure | 11.07.2024 | Examination requested [2024/49] | Fees paid | Renewal fee | 17.12.2024 | Renewal fee patent year 03 | 16.12.2025 | Renewal fee patent year 04 |
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| Responsibility for the accuracy, completeness or quality of the data displayed under the link provided lies entirely with the Unified Patent Court. | Documents cited: | Search | [Y] US8349899 (ARTERBURN JEFFREY et al.) [Y] 1-3 * See examples 10, 11, 14 and 17 * | [Y] HARMAND LYDIE ET AL: "Recyclable catalyst for the asymmetric Henry reaction based on functionalized imidazolidine-4-one-copper(II) complexes supported by a polystyrene copolymer", TETRAHEDRON LETTERS, vol. 56, no. 45, 1 November 2015 (2015-11-01), AMSTERDAM, NL, pages 6240 - 6243, XP093082580, ISSN: 0040-4039, DOI: 10.1016/j.tetlet.2015.09.112 [Y] 1-3 * See scheme 1, page 6241 * DOI: http://dx.doi.org/10.1016/j.tetlet.2015.09.112 | [Y] YEHUDA KNOBLER ET AL: "749. Reaction of N-carboxy-alpha-amino-acid anhydrides with hydrochlorides of hydroxylamine, O-alkylhydroxylamines, and amines; syntheses of amino-hydroxamic acids, amido-oxy-peptides, and alpha-amino-acid amides", JOURNAL OF THE CHEMICAL SOCIETY (RESUMED), ROYAL SOCIETY OF CHEMISTRY, 1 January 1964 (1964-01-01), pages 3941 - 3951, XP008096536, ISSN: 0368-1769, DOI: 10.1039/JR9640003941 [Y] 1-3 * See schema, e.g. on pages 3941-3942 * DOI: http://dx.doi.org/10.1039/JR9640003941 | International search | [Y] WO2019198592 (NIPPON SODA CO et al.) [Y] 1-3 * paragraph [0176], example 2, compound 18 * | [AY] JP2017509688 (エフ．ホフマン−ラ ロシュ アーゲーＦ． ＨＯＦＦＭＡＮＮ−ＬＡ ＲＯＣＨＥ ＡＫＴＩＥＮＧＥＳＥＬＬＳＣＨＡＦＴ et al.) [A] 3 [Y] 1-2 | [AY] JP2009173621 (NISSAN CHEMICAL IND LTD et al.) [A] 2 [Y] 1, 3 | [AY] JP2013537914 [A] 2 [Y] 1, 3 | [AY] JP2008545660 [A] 2 [Y] 1, 3 | [Y] US8349899 (ARTERBURN JEFFREY et al.) [Y] 1-3 * claims, examples 10, 11, 14 * | [Y] YEHUDA KNOBLER; SHMUEL BITTNER; MAX FRANKEL: "749. Reaction of N-carboxy-alpha-amino-acid anhydrides with hydrochlorides of hydroxylamine, O-alkylhydroxylamines, and amines; syntheses of amino-hydroxamic acids, amido-oxy-peptides, and alpha-amino-acid amides", JOURNAL OF THE CHEMICAL SOCIETY, 1 January 1964 (1964-01-01), pages 3941 - 3951, XP008096536, ISSN: 0368-1769, DOI: 10.1039/JR9640003941 [Y] 1-3 * page 3941, drawings, Amino-acid amides; Basicity and Steric Factors, General Procedure for the Preparation of Amino-acid amide Hydrochlorides (VIII) and of amino-acid amide (IX) * DOI: http://dx.doi.org/10.1039/JR9640003941 | [Y] HARMAND LYDIE, DRABINA PAVEL, PEJCHAL VLADIMR, HUSKOV LENKA, SEDLK MILO: "Recyclable catalyst for the asymmetric Henry reaction based on functionalized imidazolidine-4-one-copper(II) complexes supported by a polystyrene copolymer", TETRAHEDRON LETTERS, ELSEVIER, AMSTERDAM , NL, vol. 56, no. 45, 1 November 2015 (2015-11-01), Amsterdam , NL , pages 6240 - 6243, XP093082580, ISSN: 0040-4039, DOI: 10.1016/j.tetlet.2015.09.112 [Y] 1-3 * scheme 1, compound 2 * DOI: http://dx.doi.org/10.1016/j.tetlet.2015.09.112 | by applicant | JP2009173621 | WO2006127587 | WO2019198592 | ENDO ET AL.: "Development of a-Amino Acid N-carboxylic Anhydride (NCA) Synthesis Method by Phosgene-free Method and its Application to Polypeptide Synthesis", JOURNAL OF THE JAPAN ADHESION SOCIETY, vol. 52, no. 11, 2016, pages 333 - 341 [Y] 1, 3 | OLGA SCHAFER ET AL.: "Combining Orthogonal Reactive Groups in Block Copolymers for Functional Nanoparticle Synthesis in a Single Step", ACS MACRO LETT., vol. 6, 2017, pages 1140 - 1145, XP093117943, DOI: 10.1021/acsmacrolett.7b00678 [Y] 1, 3 DOI: http://dx.doi.org/10.1021/acsmacrolett.7b00678 | JAN FREUDENBERG ET AL.: "Chirality Control of Screw-Sense in Aib-Polymers: Synthesis and Helicity of Amino Acid Functionalized Polymers", ACSMACRO LETT., vol. 9, 2020, pages 686 - 692 | OYA ET AL.: "Acylation Reaction Using N-carboxyamino Acid Anhydride", ORGANIC SYNTHETIC CHEMISTRY, vol. 29, no. 8, 1971, pages 751 - 759 [Y] 1-3 * page 3941, drawings, Amino-acid amides; Basicity and Steric Factors, General Procedure for the Preparation of Amino-acid amide Hydrochlorides (VIII) and of amino-acid amide (IX) * |