JP2007516946A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2007516946A5 JP2007516946A5 JP2006518378A JP2006518378A JP2007516946A5 JP 2007516946 A5 JP2007516946 A5 JP 2007516946A5 JP 2006518378 A JP2006518378 A JP 2006518378A JP 2006518378 A JP2006518378 A JP 2006518378A JP 2007516946 A5 JP2007516946 A5 JP 2007516946A5
- Authority
- JP
- Japan
- Prior art keywords
- dinorpreg
- ethyl
- water
- oxime
- acetoxy
- 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
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 8
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 claims 6
- 238000000034 method Methods 0.000 claims 6
- 239000000047 product Substances 0.000 claims 5
- 238000006243 chemical reaction Methods 0.000 claims 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims 2
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 claims 2
- 239000003610 charcoal Substances 0.000 claims 2
- 239000012459 cleaning agent Substances 0.000 claims 2
- 238000001914 filtration Methods 0.000 claims 2
- 229960004400 levonorgestrel Drugs 0.000 claims 2
- 239000012299 nitrogen atmosphere Substances 0.000 claims 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims 2
- 239000011541 reaction mixture Substances 0.000 claims 2
- 238000003756 stirring Methods 0.000 claims 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 claims 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims 1
- HMNQNULAYXDEEQ-UHFFFAOYSA-N acetic acid;hydroxylamine Chemical compound ON.CC(O)=O HMNQNULAYXDEEQ-UHFFFAOYSA-N 0.000 claims 1
- 230000021736 acetylation Effects 0.000 claims 1
- 238000006640 acetylation reaction Methods 0.000 claims 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 claims 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims 1
- 239000012298 atmosphere Substances 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 239000006227 byproduct Substances 0.000 claims 1
- 239000012043 crude product Substances 0.000 claims 1
- QGFRSPMTVBPWNK-UHFFFAOYSA-N dilithium;oxygen(2-);hydrate Chemical compound [Li+].[Li+].O.[O-2] QGFRSPMTVBPWNK-UHFFFAOYSA-N 0.000 claims 1
- -1 enol acetate enol Chemical class 0.000 claims 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 claims 1
- 230000007062 hydrolysis Effects 0.000 claims 1
- 238000006460 hydrolysis reaction Methods 0.000 claims 1
- WTDHULULXKLSOZ-UHFFFAOYSA-N hydroxylamine hydrochloride Substances Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 claims 1
- WCYJQVALWQMJGE-UHFFFAOYSA-M hydroxylammonium chloride Chemical compound [Cl-].O[NH3+] WCYJQVALWQMJGE-UHFFFAOYSA-M 0.000 claims 1
- 239000011261 inert gas Substances 0.000 claims 1
- 238000006146 oximation reaction Methods 0.000 claims 1
- 125000004043 oxo group Chemical group O=* 0.000 claims 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims 1
- 239000000741 silica gel Substances 0.000 claims 1
- 229910002027 silica gel Inorganic materials 0.000 claims 1
- 239000001632 sodium acetate Substances 0.000 claims 1
- 235000017281 sodium acetate Nutrition 0.000 claims 1
- 239000007858 starting material Substances 0.000 claims 1
- 239000000725 suspension Substances 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- 230000002194 synthesizing effect Effects 0.000 claims 1
- 235000005074 zinc chloride Nutrition 0.000 claims 1
- 239000011592 zinc chloride Substances 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU0301982A HUP0301982A2 (hu) | 2003-06-30 | 2003-06-30 | Eljárás nagy tisztaságú d-(17alfa)-13-etil-17-hidroxi-18,19-dinor-pregn-4-én-20-in-3-on-oxim előállítására |
| PCT/HU2004/000031 WO2005000868A1 (en) | 2003-06-30 | 2004-04-29 | Process for the synthesis of high purity d-(17alpha)-13-ethyl-17hydroxy-18,19-dinorpre:gn-4-ene-20-yne-3-one-oxime |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007516946A JP2007516946A (ja) | 2007-06-28 |
| JP2007516946A5 true JP2007516946A5 (https=) | 2007-08-09 |
Family
ID=90001694
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006518378A Pending JP2007516946A (ja) | 2003-06-30 | 2004-04-29 | 高純度ｄ−（１７α）−１３−エチル−１７−ヒドロキシ−１８，１９−ジノル−プレグ−４−エン−２０−イン−３−オン−オキシムの合成方法 |
Country Status (17)
| Country | Link |
|---|---|
| EP (1) | EP1638988B1 (https=) |
| JP (1) | JP2007516946A (https=) |
| CN (1) | CN100355771C (https=) |
| AT (1) | ATE462712T1 (https=) |
| AU (1) | AU2004251118A1 (https=) |
| BR (1) | BRPI0412186A (https=) |
| CA (1) | CA2528952A1 (https=) |
| DE (1) | DE602004026306D1 (https=) |
| EA (1) | EA008411B1 (https=) |
| HR (1) | HRP20060038A2 (https=) |
| HU (1) | HUP0301982A2 (https=) |
| MX (1) | MXPA05013948A (https=) |
| NO (1) | NO20060455L (https=) |
| NZ (1) | NZ544378A (https=) |
| RS (1) | RS20050897A (https=) |
| UA (1) | UA80059C2 (https=) |
| WO (1) | WO2005000868A1 (https=) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7816546B2 (en) | 2003-06-30 | 2010-10-19 | Richter Gedeon Vegyeszeti Gyar Rt. | Process for the synthesis of high purity d-(17α)-13-ethyl-17-hydroxy-18,19-dinorpregn-4-ene-20-yn-3-one-oxime |
| ITMI20052464A1 (it) | 2005-12-22 | 2007-06-23 | S N I F F Italia S P A | Procedimento per la preparazi9one di norelgestromin norelgestromina |
| CN108827950B (zh) * | 2018-05-31 | 2020-08-21 | 成都市科隆化学品有限公司 | 乙酸中微量乙酸酐的检测方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL7306609A (https=) * | 1972-05-26 | 1973-11-28 | ||
| US4027019A (en) * | 1975-07-24 | 1977-05-31 | Ortho Pharmaceutical Corporation | 3-Oximes of D-17α-ethynyl-19-nortestosterone esters and method |
| CA2222133C (en) * | 1995-06-07 | 2002-12-24 | Cygnus, Inc. | Transdermal patch and method for administering 17-deacetyl norgestimate alone or in combination with an estrogen |
-
2003
- 2003-06-30 HU HU0301982A patent/HUP0301982A2/hu unknown
-
2004
- 2004-04-29 CN CNB2004800165780A patent/CN100355771C/zh not_active Expired - Fee Related
- 2004-04-29 MX MXPA05013948A patent/MXPA05013948A/es active IP Right Grant
- 2004-04-29 NZ NZ544378A patent/NZ544378A/en unknown
- 2004-04-29 WO PCT/HU2004/000031 patent/WO2005000868A1/en not_active Ceased
- 2004-04-29 BR BRPI0412186-4A patent/BRPI0412186A/pt not_active IP Right Cessation
- 2004-04-29 AT AT04730316T patent/ATE462712T1/de not_active IP Right Cessation
- 2004-04-29 AU AU2004251118A patent/AU2004251118A1/en not_active Abandoned
- 2004-04-29 RS YUP-2005/0897A patent/RS20050897A/sr unknown
- 2004-04-29 UA UAA200600812A patent/UA80059C2/uk unknown
- 2004-04-29 CA CA002528952A patent/CA2528952A1/en not_active Abandoned
- 2004-04-29 DE DE602004026306T patent/DE602004026306D1/de not_active Expired - Fee Related
- 2004-04-29 EP EP04730316A patent/EP1638988B1/en not_active Expired - Lifetime
- 2004-04-29 JP JP2006518378A patent/JP2007516946A/ja active Pending
- 2004-04-29 EA EA200600119A patent/EA008411B1/ru not_active IP Right Cessation
- 2004-04-29 HR HR20060038A patent/HRP20060038A2/xx not_active Application Discontinuation
-
2006
- 2006-01-27 NO NO20060455A patent/NO20060455L/no not_active Application Discontinuation
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP1301526B1 (en) | Oxidation process for preparing the intermediate 6.alpha.,9.alpha.-difluoro-11.beta.,17.alpha.-dihydroxy-16.alpha.-methyl-androst-1,4-dien-3-one 17.beta.-carboxylic acid | |
| CA2851399A1 (en) | Ulipristal acetate preparation method and intermediate thereof | |
| AU2001270906A1 (en) | Oxidation process for preparing the intermediate 6.alpha.,9.alpha.-difluoro-11.beta.,17.alpha.-dihydroxy-16.a lpha.-methyl-androst-1,4-dien-3-one 17.beta.-carboxylic acid | |
| CN115884978A (zh) | 制备胆酸衍生物的方法及其原料 | |
| JPS5842878B2 (ja) | １２−オキソコラン酸トシルヒドラゾン化合物、その製法ならびに利用 | |
| EP3712161A1 (en) | Process for preparing high puritiy allopregnanolone and intermediates thereof | |
| JPH0150704B2 (https=) | ||
| JP2007516946A5 (https=) | ||
| JP3440129B2 (ja) | グルタミン誘導体の製造法 | |
| JPH06172364A (ja) | セファロスポラン環の７−アミノ基のアシル化方法 | |
| JPS63146895A (ja) | 二水和タウロウルソデオキシコール酸の合成方法 | |
| EP1911741A1 (en) | Method for the preparation of fluticasone propionate | |
| HRP20060038A2 (en) | PROCESS FOR THE SYNTHESIS OF HIGH PURITY D-(17α)-13-ETHYL-17-HYDROXY-18,19-DINOPREGN-4-ENE-20-YNE-3-OXIME | |
| JP2000502102A (ja) | ９，１１β―エポキシドステロイドの調製方法 | |
| US4948916A (en) | Process for producing aminooxyacetic acid salts | |
| CN114195673A (zh) | 一种碘普罗胺中间体的制备方法及其用途 | |
| JP3572668B2 (ja) | アシルアミノフタル酸誘導体の製造方法 | |
| JPH06321982A (ja) | ３β−アミノコラン酸誘導体の製造方法 | |
| CN118978459B (zh) | Fmoc-L-Lys(ivDde)-OH的制备方法 | |
| CN112341354B (zh) | 一种pms的合成方法 | |
| CN101065394B (zh) | 一种硫代羟酸的酯化方法 | |
| JPH01131194A (ja) | プレグナノ［１７α，１６α−ｄ］オキサゾリン誘導体の製造法 | |
| JP4837833B2 (ja) | １，３，４−トリ−Ｏ−アシル−２−デオキシ−β−Ｄ−エリスロ−ペントピラノース類の製造方法 | |
| AU2010317895A1 (en) | Process for preparing (11beta, 16alpha)-9-fluoro-11-hydroxy-16,17-[1-methyl-ethylidenebis(oxy)]-21-[1-oxo-[4-(nitrooxymethyl) benzoxy]]pregna-1,4-dien-3,20-dione | |
| JP2002332274A (ja) | スクアラミンの製造方法 |