CA2909998A1 - Crystalline forms of 5.alpha.-androstane-3.beta.,5,6.beta.-triol and preparation methods therefor - Google Patents
Crystalline forms of 5.alpha.-androstane-3.beta.,5,6.beta.-triol and preparation methods therefor Download PDFInfo
- Publication number
- CA2909998A1 CA2909998A1 CA2909998A CA2909998A CA2909998A1 CA 2909998 A1 CA2909998 A1 CA 2909998A1 CA 2909998 A CA2909998 A CA 2909998A CA 2909998 A CA2909998 A CA 2909998A CA 2909998 A1 CA2909998 A1 CA 2909998A1
- Authority
- CA
- Canada
- Prior art keywords
- beta
- crystalline form
- solvent
- alpha
- triol
- 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.)
- Abandoned
Links
- 238000002360 preparation method Methods 0.000 title abstract description 21
- 239000013078 crystal Substances 0.000 claims description 91
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 54
- 239000002904 solvent Substances 0.000 claims description 43
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 39
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 38
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 28
- 239000002244 precipitate Substances 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 14
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 14
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 12
- 238000007865 diluting Methods 0.000 claims description 11
- 230000007704 transition Effects 0.000 claims description 11
- 238000010790 dilution Methods 0.000 claims description 10
- 239000012895 dilution Substances 0.000 claims description 10
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 239000003208 petroleum Substances 0.000 claims description 6
- 238000001816 cooling Methods 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 2
- 238000000634 powder X-ray diffraction Methods 0.000 abstract description 26
- 230000000694 effects Effects 0.000 abstract description 2
- 238000002844 melting Methods 0.000 abstract description 2
- 230000008018 melting Effects 0.000 abstract description 2
- 238000010586 diagram Methods 0.000 description 22
- 238000000113 differential scanning calorimetry Methods 0.000 description 20
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000003814 drug Substances 0.000 description 6
- 229940079593 drug Drugs 0.000 description 6
- 239000007787 solid Substances 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 238000004455 differential thermal analysis Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 239000008186 active pharmaceutical agent Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 230000000324 neuroprotective effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 150000003431 steroids Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
- C07J1/0003—Androstane derivatives
- C07J1/0007—Androstane derivatives not substituted in position 17
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Steroid Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201210060611.6 | 2012-03-08 | ||
| CN201210060611.6A CN102617685B (zh) | 2012-03-08 | 2012-03-08 | 雄甾-3β,5α,6β-三醇的晶型化合物及其制备方法 |
| CA2866398A CA2866398C (en) | 2012-03-08 | 2012-04-11 | Crystalline forms of 5.alpha.-androstane-3.beta.,5,6.beta.-triol and preparation methods therefor |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2866398A Division CA2866398C (en) | 2012-03-08 | 2012-04-11 | Crystalline forms of 5.alpha.-androstane-3.beta.,5,6.beta.-triol and preparation methods therefor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2909998A1 true CA2909998A1 (en) | 2013-09-12 |
Family
ID=46557937
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2909998A Abandoned CA2909998A1 (en) | 2012-03-08 | 2012-04-11 | Crystalline forms of 5.alpha.-androstane-3.beta.,5,6.beta.-triol and preparation methods therefor |
| CA2866398A Active CA2866398C (en) | 2012-03-08 | 2012-04-11 | Crystalline forms of 5.alpha.-androstane-3.beta.,5,6.beta.-triol and preparation methods therefor |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2866398A Active CA2866398C (en) | 2012-03-08 | 2012-04-11 | Crystalline forms of 5.alpha.-androstane-3.beta.,5,6.beta.-triol and preparation methods therefor |
Country Status (13)
| Country | Link |
|---|---|
| US (3) | US9688716B2 (enExample) |
| EP (2) | EP3112374A1 (enExample) |
| JP (1) | JP2015511587A (enExample) |
| KR (1) | KR20150002653A (enExample) |
| CN (4) | CN102617685B (enExample) |
| AU (1) | AU2012372640B2 (enExample) |
| CA (2) | CA2909998A1 (enExample) |
| IL (1) | IL234492A (enExample) |
| IN (1) | IN2014DN08198A (enExample) |
| RU (1) | RU2608894C2 (enExample) |
| SG (1) | SG11201405376TA (enExample) |
| TW (1) | TW201336861A (enExample) |
| WO (1) | WO2013131305A1 (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101742858B1 (ko) * | 2012-05-07 | 2017-06-01 | 더 프록터 앤드 갬블 캄파니 | 가요성 용기 |
| CN109985048B (zh) * | 2017-12-29 | 2021-06-29 | 广州市赛普特医药科技股份有限公司 | 2β,3α,5α-三羟基雄甾-6-酮用于炎症反应的治疗 |
| US11532903B2 (en) * | 2021-04-01 | 2022-12-20 | Ideal Industries, Inc. | Universal electrical connector |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2191576A (en) | 1936-11-21 | 1940-02-27 | Soc Of Chemical Ind | 3,5,6-trihydroxy androstane and pregnane compounds |
| US2191578A (en) | 1939-07-24 | 1940-02-27 | Crosley Corp | Ice-cream tray |
| DE3265852D1 (en) * | 1981-09-21 | 1985-10-03 | Schering Ag | 3-beta,7-beta,15-alpha-trihydroxy-5-androsten-17-one, its 3,15-dipivalate, and its preparation |
| US6046185A (en) * | 1996-07-11 | 2000-04-04 | Inflazyme Pharmaceuticals Ltd. | 6,7-oxygenated steroids and uses related thereto |
| CN101884638B (zh) * | 2010-07-09 | 2011-11-09 | 中山大学 | 5α-雄甾(烷)-3β,5,6β-三醇在制备神经元保护药物中的应用 |
| CN101961311B (zh) | 2010-09-21 | 2012-11-21 | 中山大学 | 一种5α-雄甾(烷)-3β,5,6β-三醇注射剂及其制备方法 |
| CN102180928B (zh) * | 2011-03-15 | 2013-01-16 | 广州市赛普特医药科技有限公司 | 3β,5α,6β-三羟基甾体化合物及其合成方法和应用 |
-
2012
- 2012-03-08 CN CN201210060611.6A patent/CN102617685B/zh active Active
- 2012-03-08 CN CN201310393373.5A patent/CN103626819B/zh active Active
- 2012-03-08 CN CN201310393026.2A patent/CN103626818B/zh active Active
- 2012-03-08 CN CN201310392426.1A patent/CN103626817B/zh active Active
- 2012-04-11 CA CA2909998A patent/CA2909998A1/en not_active Abandoned
- 2012-04-11 EP EP16184231.5A patent/EP3112374A1/en not_active Ceased
- 2012-04-11 US US14/383,405 patent/US9688716B2/en active Active
- 2012-04-11 WO PCT/CN2012/073854 patent/WO2013131305A1/zh not_active Ceased
- 2012-04-11 AU AU2012372640A patent/AU2012372640B2/en active Active
- 2012-04-11 CA CA2866398A patent/CA2866398C/en active Active
- 2012-04-11 IN IN8198DEN2014 patent/IN2014DN08198A/en unknown
- 2012-04-11 JP JP2014560211A patent/JP2015511587A/ja active Pending
- 2012-04-11 KR KR1020147028362A patent/KR20150002653A/ko not_active Ceased
- 2012-04-11 EP EP12870566.2A patent/EP2889303A4/en not_active Withdrawn
- 2012-04-11 SG SG11201405376TA patent/SG11201405376TA/en unknown
- 2012-04-11 RU RU2014136891A patent/RU2608894C2/ru active
-
2013
- 2013-03-07 TW TW102108093A patent/TW201336861A/zh unknown
-
2014
- 2014-09-07 IL IL234492A patent/IL234492A/en active IP Right Grant
-
2017
- 2017-05-08 US US15/589,228 patent/US9944672B2/en active Active
- 2017-05-08 US US15/589,268 patent/US9944673B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| CN102617685B (zh) | 2014-01-22 |
| IN2014DN08198A (enExample) | 2015-05-01 |
| AU2012372640A1 (en) | 2014-09-25 |
| RU2014136891A (ru) | 2016-05-10 |
| EP2889303A4 (en) | 2016-02-17 |
| CA2866398A1 (en) | 2013-09-12 |
| CN103626818A (zh) | 2014-03-12 |
| US9944672B2 (en) | 2018-04-17 |
| CN103626818B (zh) | 2016-03-30 |
| IL234492A (en) | 2017-02-28 |
| CN102617685A (zh) | 2012-08-01 |
| WO2013131305A1 (zh) | 2013-09-12 |
| EP2889303A1 (en) | 2015-07-01 |
| CA2866398C (en) | 2016-06-28 |
| CN103626817B (zh) | 2016-01-20 |
| RU2608894C2 (ru) | 2017-01-26 |
| JP2015511587A (ja) | 2015-04-20 |
| CN103626817A (zh) | 2014-03-12 |
| SG11201405376TA (en) | 2014-11-27 |
| US20150045566A1 (en) | 2015-02-12 |
| US9944673B2 (en) | 2018-04-17 |
| EP3112374A1 (en) | 2017-01-04 |
| CN103626819A (zh) | 2014-03-12 |
| CN103626819B (zh) | 2016-01-20 |
| TW201336861A (zh) | 2013-09-16 |
| US9688716B2 (en) | 2017-06-27 |
| US20170305958A1 (en) | 2017-10-26 |
| US20170305957A1 (en) | 2017-10-26 |
| AU2012372640B2 (en) | 2015-07-09 |
| KR20150002653A (ko) | 2015-01-07 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request |
Effective date: 20161027 |
|
| FZDE | Dead |
Effective date: 20201123 |