JP2012512885A5 - - Google Patents
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- JP2012512885A5 JP2012512885A5 JP2011542413A JP2011542413A JP2012512885A5 JP 2012512885 A5 JP2012512885 A5 JP 2012512885A5 JP 2011542413 A JP2011542413 A JP 2011542413A JP 2011542413 A JP2011542413 A JP 2011542413A JP 2012512885 A5 JP2012512885 A5 JP 2012512885A5
- Authority
- JP
- Japan
- Prior art keywords
- ethyl
- benzyloxyimino
- azetidine
- cyclohexyl
- benzyl
- 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
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- 238000000634 powder X-ray diffraction Methods 0.000 claims 12
- -1 4- {1-[(E) -4-cyclohexyl-3-trifluoromethyl-benzyloxyimino] -ethyl} -2-ethyl-benzyl Chemical group 0.000 claims 7
- KIHYPELVXPAIDH-APTWKGOFSA-N 1-[[4-[(Z)-N-[[4-cyclohexyl-3-(trifluoromethyl)phenyl]methoxy]-C-methylcarbonimidoyl]-2-ethylphenyl]methyl]azetidine-3-carboxylic acid Chemical compound CCC1=CC(C(\C)=N/OCC=2C=C(C(C3CCCCC3)=CC=2)C(F)(F)F)=CC=C1CN1CC(C(O)=O)C1 KIHYPELVXPAIDH-APTWKGOFSA-N 0.000 claims 4
- 150000003892 tartrate salts Chemical class 0.000 claims 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 2
- 229940049920 malate Drugs 0.000 claims 2
- 150000003891 oxalate salts Chemical class 0.000 claims 2
- KIHYPELVXPAIDH-HNSNBQBZSA-N 1-[[4-[(E)-N-[[4-cyclohexyl-3-(trifluoromethyl)phenyl]methoxy]-C-methylcarbonimidoyl]-2-ethylphenyl]methyl]azetidine-3-carboxylic acid Chemical compound CCC1=CC(C(\C)=N\OCC=2C=C(C(C3CCCCC3)=CC=2)C(F)(F)F)=CC=C1CN1CC(C(O)=O)C1 KIHYPELVXPAIDH-HNSNBQBZSA-N 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 230000000240 adjuvant Effects 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-L malate(2-) Chemical compound [O-]C(=O)C(O)CC([O-])=O BJEPYKJPYRNKOW-UHFFFAOYSA-L 0.000 claims 1
- 150000004701 malic acid derivatives Chemical class 0.000 claims 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-L oxalate Chemical compound [O-]C(=O)C([O-])=O MUBZPKHOEPUJKR-UHFFFAOYSA-L 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000011780 sodium chloride Substances 0.000 claims 1
Claims (16)
- 1−(4−{1−[(E)−4−シクロヘキシル−3−トリフルオロメチル−ベンジルオキシイミノ]−エチル}−2−エチル−ベンジル)−アゼチジン−3−カルボン酸の塩酸塩。
- 実質的に結晶性である、請求項1に記載の1−(4−{1−[(E)−4−シクロヘキシル−3−トリフルオロメチル−ベンジルオキシイミノ]−エチル}−2−エチル−ベンジル)−アゼチジン−3−カルボン酸の塩酸塩。
- 1−(4−{1−[(E)−4−シクロヘキシル−3−トリフルオロメチル−ベンジルオキシイミノ]−エチル}−2−エチル−ベンジル)−アゼチジン−3−カルボン酸の塩酸塩の結晶形態A。
- 結晶形態が、概ね2θ=8.1°、12.2°、15.8°、18.9°または19.7°に少なくとも1つの特異ピークを示す粉末X線回折パターンを有することを特徴とする、請求項3に記載の1−(4−{1−[(E)−4−シクロヘキシル−3−トリフルオロメチル−ベンジルオキシイミノ]−エチル}−2−エチル−ベンジル)−アゼチジン−3−カルボン酸の塩酸塩の結晶形態A。
- 結晶形態が、図1に示される粉末X線回折パターンと実質的に同じ粉末X線回折パターンを有することを特徴とする、請求項3または4に記載の1−(4−{1−[(E)−4−シクロヘキシル−3−トリフルオロメチル−ベンジルオキシイミノ]−エチル}−2−エチル−ベンジル)−アゼチジン−3−カルボン酸の塩酸塩の結晶形態A。
- 1−(4−{1−[(E)−4−シクロヘキシル−3−トリフルオロメチル−ベンジルオキシイミノ]−エチル}−2−エチル−ベンジル)−アゼチジン−3−カルボン酸のリンゴ酸塩。
- 結晶形態が、概ね2θ=6.8°、13.7°、15.8°、17.2°または20.5°に少なくとも1つの特異ピークを示す粉末X線回折パターンを有することを特徴とする、請求項6に記載の1−(4−{1−[(E)−4−シクロヘキシル−3−トリフルオロメチル−ベンジルオキシイミノ]−エチル}−2−エチル−ベンジル)−アゼチジン−3−カルボン酸のリンゴ酸塩の結晶形態A。
- 結晶形態が、図2に示される粉末X線回折パターンと実質的に同じ粉末X線回折パターンを有することを特徴とする、請求項7に記載の1−(4−{1−[(E)−4−シクロヘキシル−3−トリフルオロメチル−ベンジルオキシイミノ]−エチル}−2−エチル−ベンジル)−アゼチジン−3−カルボン酸のリンゴ酸塩の結晶形態A。
- 1−(4−{1−[(E)−4−シクロヘキシル−3−トリフルオロメチル−ベンジルオキシイミノ]−エチル}−2−エチル−ベンジル)−アゼチジン−3−カルボン酸のシュウ酸塩。
- 結晶形態が、概ね2θ=7.3°に少なくとも1つの特異ピークを示す粉末X線回折パターンを有することを特徴とする、請求項9に記載の1−(4−{1−[(E)−4−シクロヘキシル−3−トリフルオロメチル−ベンジルオキシイミノ]−エチル}−2−エチル−ベンジル)−アゼチジン−3−カルボン酸のシュウ酸塩の結晶形態A。
- 結晶形態が、図3に示される粉末X線回折パターンと実質的に同じ粉末X線回折パターンを有することを特徴とする、請求項10に記載の1−(4−{1−[(E)−4−シクロヘキシル−3−トリフルオロメチル−ベンジルオキシイミノ]−エチル}−2−エチル−ベンジル)−アゼチジン−3−カルボン酸のシュウ酸塩の結晶形態A。
- 1−(4−{1−[(E)−4−シクロヘキシル−3−トリフルオロメチル−ベンジルオキシイミノ]−エチル}−2−エチル−ベンジル)−アゼチジン−3−カルボン酸の酒石酸塩。
- 結晶形態が、概ね2θ=6.8°、13.6°または17.9°に少なくとも1つの特異ピークを示す粉末X線回折パターンを有することを特徴とする、請求項12に記載の1−(4−{1−[(E)−4−シクロヘキシル−3−トリフルオロメチル−ベンジルオキシイミノ]−エチル}−2−エチル−ベンジル)−アゼチジン−3−カルボン酸の酒石酸塩の結晶形態A。
- 結晶形態が、図4に示される粉末X線回折パターンと実質的に同じ粉末X線回折パターンを有することを特徴とする、請求項13に記載の1−(4−{1−[(E)−4−シクロヘキシル−3−トリフルオロメチル−ベンジルオキシイミノ]−エチル}−2−エチル−ベンジル)−アゼチジン−3−カルボン酸の酒石酸塩の結晶形態A。
- 薬学的に許容されるアジュバント、希釈剤または担体と混合された、請求項1〜14のいずれか1項に記載の1−(4−{1−[(E)−4−シクロヘキシル−3−トリフルオロメチル−ベンジルオキシイミノ]−エチル}−2−エチル−ベンジル)−アゼチジン−3−カルボン酸の塩を含む、医薬組成物。
- 医薬として使用するための請求項1〜14のいずれか1項に記載の1−(4−{1−[(E)−4−シクロヘキシル−3−トリフルオロメチル−ベンジルオキシイミノ]−エチル}−2−エチル−ベンジル)−アゼチジン−3−カルボン酸の塩。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US20305108P | 2008-12-18 | 2008-12-18 | |
US61/203,051 | 2008-12-18 | ||
PCT/US2009/068352 WO2010080455A1 (en) | 2008-12-18 | 2009-12-17 | New salts |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2012512885A JP2012512885A (ja) | 2012-06-07 |
JP2012512885A5 true JP2012512885A5 (ja) | 2012-11-22 |
Family
ID=42316715
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2011542413A Pending JP2012512885A (ja) | 2008-12-18 | 2009-12-17 | 新規な塩 |
Country Status (12)
Country | Link |
---|---|
US (2) | US8486930B2 (ja) |
EP (1) | EP2379499B1 (ja) |
JP (1) | JP2012512885A (ja) |
KR (1) | KR20110101159A (ja) |
CN (2) | CN103204794A (ja) |
AU (1) | AU2009335887A1 (ja) |
BR (1) | BRPI0922466A2 (ja) |
CA (1) | CA2747558A1 (ja) |
ES (1) | ES2478842T3 (ja) |
MX (1) | MX2011006622A (ja) |
RU (1) | RU2011129229A (ja) |
WO (1) | WO2010080455A1 (ja) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
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CN103003253A (zh) * | 2010-08-05 | 2013-03-27 | 贝林格尔.英格海姆国际有限公司 | 2-{2-[[(4-甲氧基-2,6-二甲基苯基)磺酰基]-(甲基)氨基]乙氧基}-n-甲基-n-[3-(4-甲基哌嗪-1-基)环己基]乙酰胺的酸加成盐及其作为缓激肽b1受体拮抗剂的用途 |
JO3619B1 (ar) * | 2011-01-07 | 2020-08-27 | Novartis Ag | صياغات مثبطة للمناعة |
WO2012095853A1 (en) | 2011-01-10 | 2012-07-19 | Novartis Pharma Ag | Modified release formulations comprising sip receptor modulators |
CA2973540A1 (en) | 2015-02-26 | 2016-09-01 | Novartis Ag | Treatment of autoimmune disease in a patient receiving additionally a beta-blocker |
EP3400211A1 (en) | 2016-01-04 | 2018-11-14 | Auspex Pharmaceuticals, Inc. | Azetidine modulators of the sphingosine 1-phosphate receptor |
US11958805B2 (en) * | 2017-03-09 | 2024-04-16 | Novartis Ag | Solid forms comprising an oxime ether compound, compositions and methods of use thereof |
US11629124B2 (en) * | 2017-03-09 | 2023-04-18 | Novartis Ag | Solid forms comprising an oxime ether compound, compositions and methods of use thereof |
CN111405897A (zh) | 2017-09-27 | 2020-07-10 | 雷迪博士实验室有限公司 | 辛波莫德、其盐及其固态形式的制备方法 |
AU2018341154A1 (en) | 2017-09-29 | 2020-03-12 | Novartis Ag | Dosing regimen of siponimod |
MX2020007326A (es) | 2017-09-29 | 2020-09-07 | Novartis Ag | Regimen de dosificacion de siponimod. |
US11673860B2 (en) | 2018-01-22 | 2023-06-13 | Teva Pharmaceuticals International Gmbh | Crystalline siponimod fumaric acid and polymorphs thereof |
CN110776450B (zh) * | 2018-07-27 | 2022-09-27 | 广东东阳光药业有限公司 | 一种辛波莫德晶型及其制备方法 |
WO2020234423A1 (en) | 2019-05-21 | 2020-11-26 | Synthon B.V. | Siponimod maleic acid and fumaric acid salt |
IL292529A (en) | 2019-10-31 | 2022-06-01 | Idorsia Pharmaceuticals Ltd | Combination of cxcr7 antagonist with s1p1 receptor modulator |
US11135197B2 (en) | 2020-02-07 | 2021-10-05 | Argentum Pharmaceuticals Llc | Dosage regimen of an S1P receptor modulator |
US20240010616A1 (en) | 2020-09-25 | 2024-01-11 | Synthon B.V. | Siponimod salts and cocrystals |
CN112402610A (zh) * | 2020-11-20 | 2021-02-26 | 睿阜隆(杭州)生物医药有限公司 | 1-磷酸鞘氨醇受体调节剂在制备治疗糖尿病的药物中的新用途 |
EP4212156A1 (en) | 2022-01-13 | 2023-07-19 | Abivax | Combination of 8-chloro-n-(4-(trifluoromethoxy)phenyl)quinolin-2-amine and its derivatives with a s1p receptor modulator |
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-
2009
- 2009-12-17 BR BRPI0922466A patent/BRPI0922466A2/pt not_active IP Right Cessation
- 2009-12-17 EP EP09793424.4A patent/EP2379499B1/en active Active
- 2009-12-17 CN CN2013101141799A patent/CN103204794A/zh active Pending
- 2009-12-17 CN CN2009801504811A patent/CN102256941A/zh active Pending
- 2009-12-17 CA CA2747558A patent/CA2747558A1/en not_active Abandoned
- 2009-12-17 MX MX2011006622A patent/MX2011006622A/es not_active Application Discontinuation
- 2009-12-17 WO PCT/US2009/068352 patent/WO2010080455A1/en active Application Filing
- 2009-12-17 JP JP2011542413A patent/JP2012512885A/ja active Pending
- 2009-12-17 RU RU2011129229/04A patent/RU2011129229A/ru not_active Application Discontinuation
- 2009-12-17 KR KR1020117013936A patent/KR20110101159A/ko not_active Application Discontinuation
- 2009-12-17 US US13/140,490 patent/US8486930B2/en active Active
- 2009-12-17 ES ES09793424.4T patent/ES2478842T3/es active Active
- 2009-12-17 AU AU2009335887A patent/AU2009335887A1/en not_active Abandoned
-
2013
- 2013-04-03 US US13/856,371 patent/US8697682B2/en active Active
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