JP4512592B2 - スフィンゴシン−1−リン酸受容体モジュレーターとしてのアミノプロパノール誘導体 - Google Patents
スフィンゴシン−1−リン酸受容体モジュレーターとしてのアミノプロパノール誘導体 Download PDFInfo
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- JP4512592B2 JP4512592B2 JP2006515899A JP2006515899A JP4512592B2 JP 4512592 B2 JP4512592 B2 JP 4512592B2 JP 2006515899 A JP2006515899 A JP 2006515899A JP 2006515899 A JP2006515899 A JP 2006515899A JP 4512592 B2 JP4512592 B2 JP 4512592B2
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- Prior art keywords
- phenyl
- methyl
- chloro
- amino
- methoxy
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- 125000000217 alkyl group Chemical group 0.000 claims description 22
- -1 chloro, fluoro, bromo, methoxy Chemical group 0.000 claims description 18
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 17
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
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- 125000001424 substituent group Chemical group 0.000 claims description 7
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- DYSVDTRRZTTYOH-AREMUKBSSA-N (2r)-2-amino-4-[3-chloro-5-methoxy-4-[2-(4-phenylphenyl)ethoxy]phenyl]-2-methylbutan-1-ol Chemical compound COC1=CC(CC[C@@](C)(N)CO)=CC(Cl)=C1OCCC1=CC=C(C=2C=CC=CC=2)C=C1 DYSVDTRRZTTYOH-AREMUKBSSA-N 0.000 claims description 3
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- PUIBZUZEPIQVDF-JOCHJYFZSA-N [(2r)-2-amino-4-[3-chloro-4-[2-(4-ethoxyphenyl)ethoxy]-5-methoxyphenyl]-2-methylbutyl] dihydrogen phosphate Chemical compound C1=CC(OCC)=CC=C1CCOC1=C(Cl)C=C(CC[C@@](C)(N)COP(O)(O)=O)C=C1OC PUIBZUZEPIQVDF-JOCHJYFZSA-N 0.000 claims 2
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Description
R1は、C1−6アルキル;ヒドロキシ、C1−2アルコキシまたは1〜6個のフッ素原子によって置換されるC1−6アルキル;C2−6アルケニル;またはC2−6アルキニルであり、
R2は、C1−10アルキル;C1−10ハロアルキル;C1−9アルコキシ;C1−9ハロアルコキシであり;前記のそれぞれは、所望により、フェニル、フェノキシ、C3−6シクロアルキル、C3−6シクロアルコキシ、ヘテロアリール、ヘテロアリールオキシ、複素環残基(ここで、フェニル、フェノキシ、C3−6シクロアルキル、C3−6シクロアルコキシ、ヘテロアリール、ヘテロアリールオキシ、複素環残基は、それぞれ、ヒドロキシ、ハロゲン、C1−4アルキル、C1−4ハロアルキル、C3−6シクロアルキル、C1−4アルコキシ、C1−4ハロアルコキシ、C3−6シクロアルコキシ、C3−6シクロアルキルC1−2アルキル、シアノ、フェニル、およびヒドロキシ、ハロゲン、C1−4アルキル、C1−4ハロアルキル、C1−4アルコキシ、またはシアノによって置換されるフェニルから選択される1〜5個の置換基によって環が置換されてもよい)によって末端の炭素原子上で置換されるか;
または式(b)
R10は、C1−6アルキルであり、そして、
R11は、C1−6アルキル;C1−10ハロアルキルであり;前記のそれぞれは、所望により、フェニル、フェノキシ、C3−6シクロアルキル、C3−6シクロアルコキシ、ヘテロアリール、ヘテロアリールオキシ、複素環残基(ここで、フェニル、フェノキシ、C3−6シクロアルキル、C3−6シクロアルコキシ、ヘテロアリール、ヘテロアリールオキシ、複素環残基は、それぞれ、ヒドロキシ、ハロゲン、C1−4アルキル、C1−4ハロアルキル、C3−6シクロアルキル、C1−4アルコキシ、C3−6シクロアルコキシ、C3−6シクロアルキルC1−2アルキル、シアノ、フェニル、およびヒドロキシ、ハロゲン、C1−4アルキル、C1−4アルコキシ、C1−4ハロアルキルまたはシアノによって置換されるフェニルから選択される1〜5個の置換基によって環が置換されてもよい)によって末端の炭素原子上で置換される]
の残基であり、
R3は、Z−X2〔ここで、Zは、CH2、CHF、CHMeまたはCF2であり、そして、X2はOHまたは式(a)
R4およびR5のそれぞれは、独立して、H;1、2または3個のハロゲン原子によって所望により置換されるC1−4アルキル;またはアシルであり、そして、
環Aは、R2によって、そして二つの更なる置換基によって、好ましくは、R2のオルト位で置換される}
の化合物を提供する。
R1〜R5は、上記の定義と同様であり、そして、
R6およびR7のそれぞれは、独立して、ヒドロキシ;ハロゲン;C1−4アルキル;C1−6シクロアルキル;C1−4アルコキシ;C1−6シクロアルコキシ;C3−6シクロアルキルC1−2アルキル;C1−4ハロアルキル;C1−4ハロアルコキシ;またはシアノである)である。
好ましくは、R6およびR7は、R2のオルト位で存在する。
1.R1は、CH3またはCH2−OH;
2.R2は、C1−7アルキルまたはC1−6アルコキシ;
4.R3は、CH2−OHまたはCH2−OPO3H2;
5.R4およびR5のいずれも水素
6.R6は、メチル、メトキシ、トリフルオロメチル、クロロ、フルオロまたはブロモ;
7.R6は、R2に対してオルト位;
8.R7は、メチル、メトキシ、トリフルオロメチル、クロロ、フルオロまたはブロモ;
9.R7は、R2に対してオルト位。
a)R3がZ−X2であって、X2がOHである式Iの化合物の場合は、
式III
の化合物に存在する保護基を除去するか、または
b)R3が、Z−X2であって、X2が式(a)の残基である式Iの化合物の場合は、
式IV
式(a’)
の化合物に存在する保護基を除去し、
そして、必要に応じて、遊離の形態で得られる式Iの化合物を所望の塩の形態に、またはその逆に塩の形態で得られる式Iの化合物を遊離の形態に変換させる、
ことを含んでなる。
式V
の化合物を変換させ、たとえば、アルキル化によって所望の残基−R2を導入することを含んでなる。式Vの化合物のアルキル化は、本分野で知られている方法に従って、たとえば、求核置換によって、たとえば、アルキル化剤X3−R2(ここで、X3はメシラート、トシラート、トリフラート、ノシラート(nosylate)、塩化物、臭化物、またはヨウ化物である)との反応によって行うことができる。アルキル化は、また、溶液中または固相支持体合成で、たとえば、式IVの化合物を樹脂に結合させることによって、HO−R2を用いて光延プロトコール(たとえば、Hughes, Organic Preparations and Procedures International 28, 127-64, 1996、または D.L. Hughes, Org. React. 42, 335, 1992に開示されているように)に従い行うことができる。もう一つの選択肢として、樹脂、たとえばポリスチレンに結合した、たとえば、トリフェニルホスフィンまたはジエチルアゾカルボキシラートを使用することができる。
RT=室温
AcOEt=酢酸エチル
Et2O=ジエチルエーテル
MS(ESI+):m/z=334/336(MH+)。
MS(ESI+):m/z=358/360(MH+)。
MS(ESI+):m/z=422/424/426(MH+)。
MS(ESI−):m/z=413/415(M−H−)。
MS(ESI+):m/z=420/422(MH+)。
MS(ESI−):m/z=498(M−H−)。
MS(ESI+):m/z=319(MH+)。
MS(ESI+):m/z=331(MH+)。
MS(ESI+):m/z=409(MH+)。
MS(ESI−):m/z=487(M−H−)。
MS(ESI+):m/z=441(MH+)。
ヒトS1P受容体EDG−1(S1P1)、EDG−3(S1P3)、EDG−5(S1P2)、EDG−6(S1P4)およびEDG−8(S1P5)に対する化合物のアゴニスト活性(Agonist activities)を試験する。機能的受容体活性化を、化合物によって誘発される、適切なヒトS1P受容体を安定に発現するトランスフェクトCHOまたはRH7777細胞から調製される膜蛋白質へのGTP[γ−35S]結合を定量化することによって評価する。使用されるアッセイ技術は、SPA(シンチレーション近接ベースアッセイ)である。要約すると、DMSOに溶解した化合物を段階希釈し、次に、50mM Hepes、100mM NaCl、10mM MgCl2、10μM GDP、0.1%無脂肪BSAおよび0.2nM GTP[γ−35S](1200Ci/mmol)の存在下で、SPA−ビーズ(Amersham-Pharmacia)によって固定化されたS1P受容体発現膜蛋白質(10−20μg/ウエル)に添加する。96ウエルのマイクロタイタープレート中で、室温で120分間インキュベーションの後、非結合GTP[γ−35S]を遠心工程により分離する。膜結合GTP[γ−35S]により誘発されたSPAビーズのルミネセンス(luminescence)を、TOPcountプレートリーダー(Packard)で定量する。EC50を、標準曲線に適合するソフトウエアーを使用して計算する。
式Iの化合物または賦形剤(vehicle)を、ラットに胃管栄養法によって経口的に投与する。血液学的モニタリングのための尾の血液を、個々の基底値を得るために−1日目、そして適用の2、6、24、48および72時間後に得る。このアッセイにおいて、式Iの化合物は、0.03〜3mg/kgの用量で投与した場合、末梢血リンパ球を減少させる。たとえば、以下の結果が得られる:
50%以上の末梢血リンパ球の減少
実施例1:0.5mg/kg経口で6時間後、>1mg/kg経口で48時間後
実施例5:0.2mg/kg経口で6時間後、>1mg/kg経口で48時間後
実施例9:0.2mg/kg経口で6時間後
1.1 処置を必要とする対象におけるリンパ球が介在する障害または疾患、たとえば上記のようなものを予防または処置する方法であり、該対象に有効量の式Iの化合物またはその薬学的に許容される塩を投与することを含んでなる方法;
Claims (12)
- 遊離の形態または塩の形態である式I
R1は、C1−6アルキルであり、
R2は、C 1−9アルコキシ、C1−9ハロアルコキシ、またはC 1−4 アルコキシまたはフェニルによって置換されたフェニルによって末端の炭素原子上で置換されたC 1−9 アルコキシであり、
R3は、−CH 2 OHまたは−CH 2 O−PO(OH) 2 であり、
R4およびR5のそれぞれは、独立して、Hであり、
環Aは、二つの更なる置換基R 6 およびR 7 によって置換され、
R 6 は、メチル、メトキシ、トリフルオロメチル、クロロ、フルオロまたはブロモであり、
R 7 は、メチル、メトキシ、トリフルオロメチル、クロロ、フルオロまたはブロモである}
の化合物。 - R 6 およびR 7 が、それぞれR 2 のオルト位に存在する請求項1に記載の化合物。
- R 6 が、メチル、トリフルオロメチル、クロロまたはブロモである請求項1〜3のいずれか一項に記載の化合物。
- R 6 が、クロロ、フルオロ、ブロモ、メトキシまたはメチルである請求項1〜3のいずれか一項に記載の化合物。
- R 7 が、メチル、トリフルオロメチル、クロロまたはブロモである請求項1〜5のいずれか一項に記載の化合物。
- R 7 が、クロロ、フルオロ、ブロモまたはトリフルオロメチルである請求項1〜5のいずれか一項に記載の化合物。
- R 2 が、C 1−6 アルコキシである請求項1〜7のいずれか一項に記載の化合物。
- 遊離の形態または塩の形態である式Iの化合物が、以下の化合物の群から選択される請求項1に記載の化合物:
(R)−2−アミノ−4−(3,5−ジクロロ−4−ペンチルオキシ−フェニル)−2−メチル−ブタン−1−オール・ヒドロトリフラート
(R)−2−アミノ−4−(3−ブロモ−5−メチル−4−ペンチルオキシ−フェニル)−2−メチル−ブタン−1−オール・ヒドロトリフラート
(R)−2−アミノ−4−(3,5−ジブロモ−4−ペンチルオキシ−フェニル)−2−メチル−ブタン−1−オール・塩酸塩
リン酸モノ−[(R)−2−アミノ−4−(3,5−ジクロロ−4−ペンチルオキシ−フェニル)−2−メチル−ブチル]エステル
(R)−2−アミノ−4−[3−クロロ−5−メトキシ−4−(4,4,5,5,5−ペンタフルオロ−ペンチルオキシ)−フェニル]−2−メチル−ブタン−1−オール・塩酸塩
リン酸モノ−{(R)−2−アミノ−4−[3−クロロ−5−メトキシ−4−(4,4,5,5,5−ペンタフルオロ−ペンチルオキシ−フェニル]−2−メチル−ブチル}エステル
(R)−2−アミノ−4−(3−クロロ−5−フルオロ−4−ペンチルオキシ−フェニル)−2−メチル−ブタン−1−オール・塩酸塩
(R)−2−アミノ−4−(3−クロロ−5−メトキシ−4−ペンチルオキシ−フェニル)−2−メチル−ブタン−1−オール・ヒドロトリフラート
(R)−2−アミノ−4−{3−クロロ−4−[2−(4−エトキシ−フェニル)−エトキシ]−5−メトキシ−フェニル}−2−メチル−ブタン−1−オール・ヒドロトリフラート
リン酸モノ−((R)−2−アミノ−4−{3−クロロ−4−[2−(4−エトキシ−フェニル)−エトキシ]−5−メトキシ−フェニル}−2−メチル−ブチル)エステル
(R)−2−アミノ−4−[4−(2−ビフェニル−4−イル−エトキシ)−3−クロロ−5−メトキシ−フェニル]−2−メチル−ブタン−1−オール・ヒドロトリフラート。 - 遊離の形態または塩の形態である式Iの化合物が、以下の化合物の群から選択される請求項1に記載の化合物:
(R)−2−アミノ−4−(3,5−ジクロロ−4−ペンチルオキシ−フェニル)−2−メチル−ブタン−1−オール・ヒドロトリフラート
リン酸モノ−[(R)−2−アミノ−4−(3,5−ジクロロ−4−ペンチルオキシ−フェニル)−2−メチル−ブチル]エステル
(R)−2−アミノ−4−[3−クロロ−5−メトキシ−4−(4,4,5,5,5−ペンタフルオロ−ペンチルオキシ)−フェニル]−2−メチル−ブタン−1−オール・塩酸塩
リン酸モノ−{(R)−2−アミノ−4−[3−クロロ−5−メトキシ−4−(4,4,5,5,5−ペンタフルオロ−ペンチルオキシ−フェニル]−2−メチル−ブチル}エステル
(R)−2−アミノ−4−{3−クロロ−4−[2−(4−エトキシ−フェニル)−エトキシ]−5−メトキシ−フェニル}−2−メチル−ブタン−1−オール・ヒドロトリフラート
リン酸モノ−((R)−2−アミノ−4−{3−クロロ−4−[2−(4−エトキシ−フェニル)−エトキシ]−5−メトキシ−フェニル}−2−メチル−ブチル)エステル。 - 薬剤として使用するためおよび薬剤の製造に使用するための請求項1〜10のいずれか一項に記載の化合物またはその薬学的に許容される塩。
- 請求項1〜10のいずれか一項に記載の化合物またはその薬学的に許容される塩をその目的のための薬学的に許容される希釈剤または担体と一緒に含んでなる薬剤組成物。
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GBGB0313612.4A GB0313612D0 (en) | 2003-06-12 | 2003-06-12 | Organic compounds |
PCT/EP2004/006318 WO2004110979A2 (en) | 2003-06-12 | 2004-06-11 | Amino-propanol derivatives as sphingosine-1-phosphate receptor modulator |
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GB0324210D0 (en) | 2003-10-15 | 2003-11-19 | Novartis Ag | Organic compounds |
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JP2008509931A (ja) | 2004-08-13 | 2008-04-03 | プレーシス ファーマスーティカルズ インコーポレイテッド | スフィンゴシン−1−ホスフェート(s1p)レセプター活性を調節するための方法および組成物 |
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GB0504544D0 (en) * | 2005-03-04 | 2005-04-13 | Novartis Ag | Organic compounds |
PT1919290E (pt) * | 2005-07-12 | 2014-03-20 | Ampio Pharmaceuticals Inc | Métodos e produtos para tratamento de doenças |
EP1932522B1 (en) * | 2005-10-07 | 2012-05-23 | Kyorin Pharmaceutical Co., Ltd. | Therapeutic agent for liver disease containing 2-amino-1,3-propanediol derivative as active ingredient |
ES2369520T3 (es) * | 2005-12-15 | 2011-12-01 | Mitsubishi Tanabe Pharma Corporation | Compuesto amínico y su uso para propósitos médicos. |
TWI389683B (zh) * | 2006-02-06 | 2013-03-21 | Kyorin Seiyaku Kk | A therapeutic agent for an inflammatory bowel disease or an inflammatory bowel disease treatment using a 2-amino-1,3-propanediol derivative as an active ingredient |
WO2008018427A1 (fr) * | 2006-08-08 | 2008-02-14 | Kyorin Pharmaceutical Co., Ltd. | Dérivé d'ester de l'acide aminophosphorique et modulateur du récepteur s1p contenant ledit dérivé en tant que principe actif |
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TW200946105A (en) | 2008-02-07 | 2009-11-16 | Kyorin Seiyaku Kk | Therapeutic agent or preventive agent for inflammatory bowel disease containing amino alcohol derivative as active ingredient |
CN102164891B (zh) | 2008-07-23 | 2014-09-03 | 艾尼纳制药公司 | 可用于治疗自身免疫性疾病和炎性疾病的经取代的1,2,3,4-四氢环戊并[b]吲哚-3-基乙酸衍生物 |
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HUE028212T2 (en) | 2009-06-22 | 2016-12-28 | Ampio Pharmaceuticals Inc | Procedure for treating diseases |
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CN102565253A (zh) * | 2010-12-16 | 2012-07-11 | 中国人民解放军第二军医大学 | 一种小分子代谢物图谱及其制作方法和用途 |
JP6033791B2 (ja) * | 2011-12-23 | 2016-11-30 | Meiji Seikaファルマ株式会社 | 新規s1p受容体調整薬 |
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AU2004247384B2 (en) | 2008-02-28 |
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US7696184B2 (en) | 2010-04-13 |
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US20070010494A1 (en) | 2007-01-11 |
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CN100358861C (zh) | 2008-01-02 |
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