JP2005501898A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2005501898A5 JP2005501898A5 JP2003524956A JP2003524956A JP2005501898A5 JP 2005501898 A5 JP2005501898 A5 JP 2005501898A5 JP 2003524956 A JP2003524956 A JP 2003524956A JP 2003524956 A JP2003524956 A JP 2003524956A JP 2005501898 A5 JP2005501898 A5 JP 2005501898A5
- Authority
- JP
- Japan
- Prior art keywords
- haloenamine
- substituted
- immobilized
- hydrocarbyl
- acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 9
- -1 phosphorus halide Chemical class 0.000 claims 9
- 150000001875 compounds Chemical class 0.000 claims 8
- 238000000034 method Methods 0.000 claims 8
- 239000007788 liquid Substances 0.000 claims 6
- 239000000203 mixture Substances 0.000 claims 6
- 125000005843 halogen group Chemical group 0.000 claims 5
- 238000004519 manufacturing process Methods 0.000 claims 5
- 150000003511 tertiary amides Chemical class 0.000 claims 5
- 239000003153 chemical reaction reagent Substances 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- 229910052698 phosphorus Inorganic materials 0.000 claims 4
- 238000000926 separation method Methods 0.000 claims 4
- 150000003573 thiols Chemical class 0.000 claims 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 3
- 239000011574 phosphorus Substances 0.000 claims 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims 2
- 239000003125 aqueous solvent Substances 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 2
- 125000005328 phosphinyl group Chemical group [PH2](=O)* 0.000 claims 2
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical group ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 claims 2
- 229920000642 polymer Polymers 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 2
- OGFAWKRXZLGJSK-UHFFFAOYSA-N 1-(2,4-dihydroxyphenyl)-2-(4-nitrophenyl)ethanone Chemical compound OC1=CC(O)=CC=C1C(=O)CC1=CC=C([N+]([O-])=O)C=C1 OGFAWKRXZLGJSK-UHFFFAOYSA-N 0.000 claims 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims 1
- 229910019142 PO4 Inorganic materials 0.000 claims 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical compound OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 claims 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 125000002252 acyl group Chemical group 0.000 claims 1
- 125000004423 acyloxy group Chemical group 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims 1
- 125000004104 aryloxy group Chemical group 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 150000004820 halides Chemical class 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 239000010452 phosphate Substances 0.000 claims 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 claims 1
- 125000004437 phosphorous atom Chemical group 0.000 claims 1
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 claims 1
- 229940124530 sulfonamide Drugs 0.000 claims 1
- 150000003456 sulfonamides Chemical class 0.000 claims 1
- 150000003462 sulfoxides Chemical class 0.000 claims 1
- 150000003512 tertiary amines Chemical class 0.000 claims 1
- 150000003566 thiocarboxylic acids Chemical class 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US31615101P | 2001-08-30 | 2001-08-30 | |
| US10/061,617 US6677487B2 (en) | 2001-08-30 | 2002-02-01 | α-haloenamine reagents |
| PCT/US2002/025609 WO2003020684A1 (en) | 2001-08-30 | 2002-08-13 | (alpha)-haloenamine reagents |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005501898A JP2005501898A (ja) | 2005-01-20 |
| JP2005501898A5 true JP2005501898A5 (enExample) | 2005-12-22 |
Family
ID=26741280
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003524956A Pending JP2005501898A (ja) | 2001-08-30 | 2002-08-13 | α−ハロエナミン試剤 |
| JP2003523216A Withdrawn JP2005506977A (ja) | 2001-08-30 | 2002-08-30 | ポリアミド合成用の芳香族及びヘテロ芳香族酸ハロゲン化物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003523216A Withdrawn JP2005506977A (ja) | 2001-08-30 | 2002-08-30 | ポリアミド合成用の芳香族及びヘテロ芳香族酸ハロゲン化物 |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US6677487B2 (enExample) |
| EP (2) | EP1421056A1 (enExample) |
| JP (2) | JP2005501898A (enExample) |
| KR (2) | KR20040029461A (enExample) |
| CN (2) | CN1561326A (enExample) |
| AU (2) | AU2002323122B2 (enExample) |
| BR (2) | BR0212553A (enExample) |
| CA (2) | CA2458859A1 (enExample) |
| IL (2) | IL160609A0 (enExample) |
| MX (2) | MXPA04001957A (enExample) |
| PL (2) | PL368829A1 (enExample) |
| RS (2) | RS26104A (enExample) |
| RU (2) | RU2004109226A (enExample) |
| WO (2) | WO2003020684A1 (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6677487B2 (en) * | 2001-08-30 | 2004-01-13 | Pharmacia Corporation | α-haloenamine reagents |
| CN102399241A (zh) * | 2010-09-09 | 2012-04-04 | 信诺美(北京)化工科技有限公司 | 一种芳香基磷酸二酯的合成方法 |
| WO2015125721A1 (ja) * | 2014-02-18 | 2015-08-27 | 日産化学工業株式会社 | 電荷輸送性ワニス |
| US20190084928A1 (en) * | 2016-04-01 | 2019-03-21 | National University Corporation Chiba University | Method for producing nitrogen-containing aromatic amide, method for producing pyrrole-imidazole polyamide, and compound |
| KR102615161B1 (ko) | 2017-03-31 | 2023-12-15 | 신젠타 파티서페이션즈 아게 | 살진균 조성물 |
| CN113754553B (zh) * | 2021-10-18 | 2022-12-13 | 江苏快达农化股份有限公司 | 一种连续法合成水杨酰胺的方法 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2638356A1 (de) | 1976-08-26 | 1978-03-02 | Bayer Ag | Verfahren zur herstellung vinylsubstituierter cyclopropancarbonsaeureester |
| DE2715336A1 (de) | 1977-04-06 | 1978-10-19 | Bayer Ag | Verfahren zur herstellung viergliedriger cyclischer ketone |
| US4794109A (en) | 1982-11-16 | 1988-12-27 | Ciba-Geigy Corporation | 6-hydroxy-lower alkylpenem compounds, pharmaceutical preparations that contain these compounds, and the use of the latter |
| DE3789581D1 (de) | 1986-07-23 | 1994-05-19 | Ciba Geigy | Komplexe mit optisch aktiven Zuckerliganden, Verfahren zu deren Herstellung und deren Verwendung. |
| US5218097A (en) | 1988-12-07 | 1993-06-08 | Ciba-Geigy Corporation | Process for the preparation of protected mono-sugar and oligo-sugar halides |
| CH681623A5 (en) * | 1990-11-05 | 1993-04-30 | Ciba Geigy Ag | Prodn. of alpha-halo:enamine halogenating agents - comprises two stage halogenation of di:substd. acetamide in presence of carboxamide or lactam catalyst and addn. of amine |
| US5459131A (en) | 1991-03-15 | 1995-10-17 | American Cyanamid Company | Renin inhibitors |
| US5643878A (en) | 1991-09-12 | 1997-07-01 | Ciba-Geigy Corporation | 5-amino-4-hydroxyhexanoic acid derivatives |
| US5273991A (en) * | 1992-07-29 | 1993-12-28 | Research Corporation Technologies, Inc. | Imidazole-containing compositions and methods of use thereof analogs of distamycin |
| US5441876A (en) | 1993-07-30 | 1995-08-15 | The United States Of America As Represented By The Secretary Of The Navy | Process for the preparation of headgroup-modified phospholipids using phosphatidylhydroxyalkanols as intermediates |
| US5514643A (en) | 1993-08-16 | 1996-05-07 | Lucky Ltd. | 2-aminothiazolecarboxamide derivatives, processes for preparing the same and use thereof for controlling phytopathogenic organisms |
| WO1996033972A1 (en) * | 1995-04-28 | 1996-10-31 | Glaxo Group Limited | Methods for synthesizing diverse collections of pyridines, pyrimidines, 1,4-dihydro derivatives thereof, and piperidine derivatives |
| GB2310207A (en) | 1996-02-15 | 1997-08-20 | Pharmacia Spa | Antiviral ureido derivatives of substituted heterocyclic compounds |
| US6090947A (en) | 1996-02-26 | 2000-07-18 | California Institute Of Technology | Method for the synthesis of pyrrole and imidazole carboxamides on a solid support |
| TW533205B (en) | 1996-06-25 | 2003-05-21 | Novartis Ag | Substituted 3,5-diphenyl-l,2,4-triazoles and their pharmaceutical composition |
| DE19805431A1 (de) | 1998-02-11 | 1999-08-12 | Merck Patent Gmbh | Heteroaromatische Oligoamide als Affinitätsliganden |
| CN1348370A (zh) | 1999-04-15 | 2002-05-08 | 布里斯托尔-迈尔斯斯奎布公司 | 环状蛋白酪氨酸激酶抑制剂 |
| US6677487B2 (en) * | 2001-08-30 | 2004-01-13 | Pharmacia Corporation | α-haloenamine reagents |
-
2002
- 2002-02-01 US US10/061,617 patent/US6677487B2/en not_active Expired - Fee Related
- 2002-08-13 EP EP02757083A patent/EP1421056A1/en not_active Withdrawn
- 2002-08-13 BR BR0212553-6A patent/BR0212553A/pt not_active IP Right Cessation
- 2002-08-13 CA CA002458859A patent/CA2458859A1/en not_active Abandoned
- 2002-08-13 MX MXPA04001957A patent/MXPA04001957A/es not_active Application Discontinuation
- 2002-08-13 CN CNA028190084A patent/CN1561326A/zh active Pending
- 2002-08-13 RS YU26104A patent/RS26104A/sr unknown
- 2002-08-13 JP JP2003524956A patent/JP2005501898A/ja active Pending
- 2002-08-13 IL IL16060902A patent/IL160609A0/xx unknown
- 2002-08-13 RU RU2004109226/04A patent/RU2004109226A/ru not_active Application Discontinuation
- 2002-08-13 AU AU2002323122A patent/AU2002323122B2/en not_active Expired - Fee Related
- 2002-08-13 PL PL02368829A patent/PL368829A1/xx not_active Application Discontinuation
- 2002-08-13 WO PCT/US2002/025609 patent/WO2003020684A1/en not_active Ceased
- 2002-08-13 KR KR10-2004-7003127A patent/KR20040029461A/ko not_active Ceased
- 2002-08-30 CA CA002458616A patent/CA2458616A1/en not_active Abandoned
- 2002-08-30 PL PL02368830A patent/PL368830A1/xx not_active Application Discontinuation
- 2002-08-30 RS YUP-260/04A patent/RS26004A/sr unknown
- 2002-08-30 KR KR10-2004-7003109A patent/KR20040029460A/ko not_active Ceased
- 2002-08-30 JP JP2003523216A patent/JP2005506977A/ja not_active Withdrawn
- 2002-08-30 WO PCT/US2002/027953 patent/WO2003018552A2/en not_active Ceased
- 2002-08-30 EP EP02796456A patent/EP1430028A2/en not_active Withdrawn
- 2002-08-30 MX MXPA04001958A patent/MXPA04001958A/es unknown
- 2002-08-30 CN CNA028192117A patent/CN1561333A/zh active Pending
- 2002-08-30 AU AU2002332809A patent/AU2002332809B2/en not_active Expired - Fee Related
- 2002-08-30 BR BR0212393-2A patent/BR0212393A/pt not_active IP Right Cessation
- 2002-08-30 IL IL16059602A patent/IL160596A0/xx unknown
- 2002-08-30 RU RU2004109225/04A patent/RU2004109225A/ru not_active Application Discontinuation
-
2003
- 2003-09-17 US US10/664,123 patent/US6924396B2/en not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ATE451380T1 (de) | Verfahren zur herstellung von bisphosphonsäureverbindungen | |
| JP4303595B2 (ja) | アニオン性置換基を有する物質を捕捉可能な亜鉛錯体 | |
| IL174323A0 (en) | Surface immobilized polyelectrolyte with multiple functional groups capable of covalently bonding to biomolecules | |
| ATE233775T1 (de) | Verfahren zur herstellung von phosphinsäureestern | |
| JP2002508428A5 (enExample) | ||
| JP2005501898A5 (enExample) | ||
| JP2007511523A5 (enExample) | ||
| JP2016521250A5 (enExample) | ||
| WO2005016115A3 (en) | Biosensors utilizing dendrimer-immobilized ligands and their use thereof | |
| WO1990011322A3 (en) | Method and reagent for sulfurization of organophosphorous compounds | |
| DE50202036D1 (de) | Verfahren zur Herstellung von Carboxyethylmethylphosphinsäureglykolester | |
| CN103492405A (zh) | 使用捕获标记物的三磷酸化寡核苷酸的纯化 | |
| ATE508134T1 (de) | Amorphe form das natriumsalzes der ibandronsäure | |
| JP2003525287A5 (ja) | 1,3-ジヒドロ-2h-インドール-2-オンならびにアルギニン-バソプレッシンのv1bまたはv1bおよびv1aの両方のレセプターのリガンドとしてのそれらの使用 | |
| DE102004025694A1 (de) | Verfahren und Oberfläche zu hochparallelen Analysen von Nukleinsäureketten | |
| ATE433985T1 (de) | Phosphorhaltige mischungen, ein verfahren zu ihrer herstellung und ihre verwendung | |
| JP2004536049A5 (enExample) | ||
| WO2004082604A3 (en) | Phosphoric ester demulsifier composition | |
| DE502004011432D1 (de) | Verfahren zur herstellung von phosphoniumsalzen | |
| JP2014516947A5 (enExample) | ||
| ES2628322T3 (es) | Compuestos de tiol y su uso para la síntesis de oligonucleótidos modificados | |
| ATE312836T1 (de) | Verfahren zur herstellung von 4-amino-1- hydroxybutyliden-1,1-bisphosphonsäure | |
| US7601848B2 (en) | Multifunctional reagent for the synthesis of thiol modified oligomers | |
| DE502007005080D1 (de) | Verfahren zur herstellung quarternärer carbonate | |
| Sobkowska et al. | Aryl H-phosphonates. 6. Synthetic studies on the preparation of nucleoside N-alkyl-H-phosphonamidates |