DE4441462C1 - Verfahren zur stereoselektiven Reduktion von 17-Oxo-Steroiden - Google Patents
Verfahren zur stereoselektiven Reduktion von 17-Oxo-SteroidenInfo
- Publication number
- DE4441462C1 DE4441462C1 DE4441462A DE4441462A DE4441462C1 DE 4441462 C1 DE4441462 C1 DE 4441462C1 DE 4441462 A DE4441462 A DE 4441462A DE 4441462 A DE4441462 A DE 4441462A DE 4441462 C1 DE4441462 C1 DE 4441462C1
- Authority
- DE
- Germany
- Prior art keywords
- methylene
- methyl ether
- estradiol
- hydroxy steroid
- reduction
- 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.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims description 22
- 238000011916 stereoselective reduction Methods 0.000 title claims description 6
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 claims abstract description 60
- 150000000179 1,2-aminoalcohols Chemical class 0.000 claims abstract description 36
- 239000003054 catalyst Substances 0.000 claims abstract description 34
- 229910000085 borane Inorganic materials 0.000 claims abstract description 30
- 238000006722 reduction reaction Methods 0.000 claims description 22
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 230000000707 stereoselective effect Effects 0.000 abstract 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 69
- 238000004128 high performance liquid chromatography Methods 0.000 description 26
- 238000001953 recrystallisation Methods 0.000 description 26
- -1 lithium aluminum hydride Chemical compound 0.000 description 13
- 238000011097 chromatography purification Methods 0.000 description 9
- GLWZHHIKYKXSQM-LLVKDONJSA-N 1-[(r)-amino(phenyl)methyl]cyclopentan-1-ol Chemical compound C1([C@@H](N)C2(O)CCCC2)=CC=CC=C1 GLWZHHIKYKXSQM-LLVKDONJSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 4
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- OGCGXUGBDJGFFY-MRXNPFEDSA-N (r)-alpha,alpha-diphenyl-2-pyrrolidinemethanol Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(O)[C@H]1CCCN1 OGCGXUGBDJGFFY-MRXNPFEDSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- MIWZUUDZNFGLRT-HNNXBMFYSA-N [(2s)-azetidin-2-yl]-diphenylmethanol Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(O)[C@@H]1CCN1 MIWZUUDZNFGLRT-HNNXBMFYSA-N 0.000 description 3
- UWTDFICHZKXYAC-UHFFFAOYSA-N boron;oxolane Chemical compound [B].C1CCOC1 UWTDFICHZKXYAC-UHFFFAOYSA-N 0.000 description 3
- OGCGXUGBDJGFFY-INIZCTEOSA-N diphenyl-[(2s)-pyrrolidin-2-yl]methanol Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(O)[C@@H]1CCCN1 OGCGXUGBDJGFFY-INIZCTEOSA-N 0.000 description 3
- 229960005309 estradiol Drugs 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- MIWZUUDZNFGLRT-OAHLLOKOSA-N [(2r)-azetidin-2-yl]-diphenylmethanol Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(O)[C@H]1CCN1 MIWZUUDZNFGLRT-OAHLLOKOSA-N 0.000 description 2
- FIGHBCGEPWLMOK-AWEZNQCLSA-N [(3r)-1,1-dioxothiazetidin-3-yl]-diphenylmethanol Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(O)[C@@H]1CS(=O)(=O)N1 FIGHBCGEPWLMOK-AWEZNQCLSA-N 0.000 description 2
- ZSKDXMLMMQFHGW-SNVBAGLBSA-N [(3r)-1,2,3,4-tetrahydroisoquinolin-3-yl]methanol Chemical compound C1=CC=C2CN[C@@H](CO)CC2=C1 ZSKDXMLMMQFHGW-SNVBAGLBSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 238000013375 chromatographic separation Methods 0.000 description 2
- 229940011871 estrogen Drugs 0.000 description 2
- 239000000262 estrogen Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 239000012279 sodium borohydride Substances 0.000 description 2
- 229910000033 sodium borohydride Inorganic materials 0.000 description 2
- 239000003270 steroid hormone Substances 0.000 description 2
- YUEFUFVJLIDEOA-KRWDZBQOSA-N (2r)-2-amino-1,1-diphenyl-3-propan-2-ylsulfanylpropan-1-ol Chemical compound C=1C=CC=CC=1C(O)([C@@H](N)CSC(C)C)C1=CC=CC=C1 YUEFUFVJLIDEOA-KRWDZBQOSA-N 0.000 description 1
- GLWZHHIKYKXSQM-NSHDSACASA-N 1-[(s)-amino(phenyl)methyl]cyclopentan-1-ol Chemical compound C1([C@H](N)C2(O)CCCC2)=CC=CC=C1 GLWZHHIKYKXSQM-NSHDSACASA-N 0.000 description 1
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 1
- FVQDOKQWEOZEBQ-UHFFFAOYSA-N B1NCCO1 Chemical class B1NCCO1 FVQDOKQWEOZEBQ-UHFFFAOYSA-N 0.000 description 1
- 229910004664 Cerium(III) chloride Inorganic materials 0.000 description 1
- BFPYWIDHMRZLRN-SLHNCBLASA-N Ethinyl estradiol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1 BFPYWIDHMRZLRN-SLHNCBLASA-N 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- VYLVYHXQOHJDJL-UHFFFAOYSA-K cerium trichloride Chemical compound Cl[Ce](Cl)Cl VYLVYHXQOHJDJL-UHFFFAOYSA-K 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- LNUDNNFEXRHHGY-DEOSSOPVSA-N dinaphthalen-2-yl-[(2s)-pyrrolidin-2-yl]methanol Chemical compound C=1C=C2C=CC=CC2=CC=1C(C=1C=C2C=CC=CC2=CC=1)(O)[C@@H]1CCCN1 LNUDNNFEXRHHGY-DEOSSOPVSA-N 0.000 description 1
- OGCGXUGBDJGFFY-UHFFFAOYSA-N diphenylprolinol Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(O)C1CCCN1 OGCGXUGBDJGFFY-UHFFFAOYSA-N 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229960003399 estrone Drugs 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 239000012280 lithium aluminium hydride Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000011946 reduction process Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 150000003431 steroids Chemical class 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000002699 waste material Substances 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
- C07J1/0051—Estrane derivatives
- C07J1/0062—Estrane derivatives substituted in position 17 alfa not substituted in position 17 beta
-
- 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
- C07J1/0051—Estrane derivatives
- C07J1/0059—Estrane derivatives substituted in position 17 by a keto group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J53/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by condensation with a carbocyclic rings or by formation of an additional ring by means of a direct link between two ring carbon atoms, including carboxyclic rings fused to the cyclopenta(a)hydrophenanthrene skeleton are included in this class
- C07J53/002—Carbocyclic rings fused
- C07J53/004—3 membered carbocyclic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Steroid Compounds (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4441462A DE4441462C1 (de) | 1994-11-22 | 1994-11-22 | Verfahren zur stereoselektiven Reduktion von 17-Oxo-Steroiden |
| DE59502492T DE59502492D1 (de) | 1994-11-22 | 1995-11-04 | Verfahren zur stereoselektiven Reduktion von 17-Oxo-Steroiden |
| AT95117386T ATE167191T1 (de) | 1994-11-22 | 1995-11-04 | Verfahren zur stereoselektiven reduktion von 17- oxo-steroiden |
| EP95117386A EP0713880B1 (de) | 1994-11-22 | 1995-11-04 | Verfahren zur stereoselektiven Reduktion von 17-Oxo-Steroiden |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4441462A DE4441462C1 (de) | 1994-11-22 | 1994-11-22 | Verfahren zur stereoselektiven Reduktion von 17-Oxo-Steroiden |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE4441462C1 true DE4441462C1 (de) | 1996-05-23 |
Family
ID=6533807
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE4441462A Expired - Lifetime DE4441462C1 (de) | 1994-11-22 | 1994-11-22 | Verfahren zur stereoselektiven Reduktion von 17-Oxo-Steroiden |
| DE59502492T Expired - Fee Related DE59502492D1 (de) | 1994-11-22 | 1995-11-04 | Verfahren zur stereoselektiven Reduktion von 17-Oxo-Steroiden |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE59502492T Expired - Fee Related DE59502492D1 (de) | 1994-11-22 | 1995-11-04 | Verfahren zur stereoselektiven Reduktion von 17-Oxo-Steroiden |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP0713880B1 (cg-RX-API-DMAC7.html) |
| AT (1) | ATE167191T1 (cg-RX-API-DMAC7.html) |
| DE (2) | DE4441462C1 (cg-RX-API-DMAC7.html) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102012016476A1 (de) | 2012-08-17 | 2014-02-20 | Max Franz | Chirale Azetidincarbonsäure-Derivate |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DD145919B1 (de) * | 1978-06-28 | 1982-06-30 | Kurt Ponsold | Verfahren zur herstellung von 14,1 -methylenderivaten der oestranreihe |
| JPS57146786A (en) * | 1981-03-09 | 1982-09-10 | Kyowa Hakko Kogyo Co Ltd | Optically active borane compound and preparation of optically active compound using the same |
| HU200755B (en) * | 1983-04-04 | 1990-08-28 | Sumitomo Chemical Co. Ltd.,Jp | Process for producing optically active alcohol derivatives by using asymmetrically modified compounds of boron hydride type |
| JPS6118790A (ja) * | 1984-07-05 | 1986-01-27 | Sumitomo Chem Co Ltd | 光学活性ボラン錯体およびその製造法 |
-
1994
- 1994-11-22 DE DE4441462A patent/DE4441462C1/de not_active Expired - Lifetime
-
1995
- 1995-11-04 EP EP95117386A patent/EP0713880B1/de not_active Expired - Lifetime
- 1995-11-04 AT AT95117386T patent/ATE167191T1/de not_active IP Right Cessation
- 1995-11-04 DE DE59502492T patent/DE59502492D1/de not_active Expired - Fee Related
Non-Patent Citations (1)
| Title |
|---|
| Tetrahedron Letters 35 (1994), 2329-2330 * |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0713880B1 (de) | 1998-06-10 |
| DE59502492D1 (de) | 1998-07-16 |
| EP0713880A3 (cg-RX-API-DMAC7.html) | 1996-06-19 |
| ATE167191T1 (de) | 1998-06-15 |
| EP0713880A2 (de) | 1996-05-29 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8100 | Publication of patent without earlier publication of application | ||
| D1 | Grant (no unexamined application published) patent law 81 | ||
| 8364 | No opposition during term of opposition | ||
| 8327 | Change in the person/name/address of the patent owner |
Owner name: JENAPHARM GMBH & CO. KG, 07745 JENA, DE |
|
| 8330 | Complete renunciation |