JP2022514347A - 置換3-((3-アミノフェニル)アミノ)ピペリジン-2,6-ジオン化合物、その組成物、及びそれを用いた治療法 - Google Patents
置換3-((3-アミノフェニル)アミノ)ピペリジン-2,6-ジオン化合物、その組成物、及びそれを用いた治療法 Download PDFInfo
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- JP2022514347A JP2022514347A JP2021535546A JP2021535546A JP2022514347A JP 2022514347 A JP2022514347 A JP 2022514347A JP 2021535546 A JP2021535546 A JP 2021535546A JP 2021535546 A JP2021535546 A JP 2021535546A JP 2022514347 A JP2022514347 A JP 2022514347A
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- piperidine
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- 150000003456 sulfonamides Chemical class 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 239000010414 supernatant solution Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 239000007916 tablet composition Substances 0.000 description 1
- 239000007885 tablet disintegrant Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 238000003419 tautomerization reaction Methods 0.000 description 1
- RCINICONZNJXQF-MZXODVADSA-N taxol Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 description 1
- CUHRQSCWDNWKOJ-NSHDSACASA-N tert-butyl (2S)-4-(2-ethoxy-2-oxoethylidene)-2-methylpiperidine-1-carboxylate Chemical compound C(C)OC(C=C1C[C@@H](N(CC1)C(=O)OC(C)(C)C)C)=O CUHRQSCWDNWKOJ-NSHDSACASA-N 0.000 description 1
- VMWRROAFENCIJX-GJZGRUSLSA-N tert-butyl (2S,4R)-4-[2-(5-amino-3-ethylpyridin-2-yl)oxyethyl]-2-methylpiperidine-1-carboxylate Chemical compound NC=1C=C(C(=NC=1)OCC[C@H]1C[C@@H](N(CC1)C(=O)OC(C)(C)C)C)CC VMWRROAFENCIJX-GJZGRUSLSA-N 0.000 description 1
- HQMYWQCBINPHBB-QMMMGPOBSA-N tert-butyl (2s)-2-methyl-4-oxopiperidine-1-carboxylate Chemical compound C[C@H]1CC(=O)CCN1C(=O)OC(C)(C)C HQMYWQCBINPHBB-QMMMGPOBSA-N 0.000 description 1
- BNWCETAHAJSBFG-UHFFFAOYSA-N tert-butyl 2-bromoacetate Chemical compound CC(C)(C)OC(=O)CBr BNWCETAHAJSBFG-UHFFFAOYSA-N 0.000 description 1
- CVAWKJKISIPBOD-UHFFFAOYSA-N tert-butyl 2-bromopropanoate Chemical compound CC(Br)C(=O)OC(C)(C)C CVAWKJKISIPBOD-UHFFFAOYSA-N 0.000 description 1
- NFEGNISFSSLEGU-UHFFFAOYSA-N tert-butyl 2-diethoxyphosphorylacetate Chemical compound CCOP(=O)(OCC)CC(=O)OC(C)(C)C NFEGNISFSSLEGU-UHFFFAOYSA-N 0.000 description 1
- HQMYWQCBINPHBB-UHFFFAOYSA-N tert-butyl 2-methyl-4-oxopiperidine-1-carboxylate Chemical compound CC1CC(=O)CCN1C(=O)OC(C)(C)C HQMYWQCBINPHBB-UHFFFAOYSA-N 0.000 description 1
- HFMHEXPZANOFSL-UHFFFAOYSA-N tert-butyl 3-(hydrazinecarbonyl)pyrrolidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCC(C(=O)NN)C1 HFMHEXPZANOFSL-UHFFFAOYSA-N 0.000 description 1
- CTEDVGRUGMPBHE-UHFFFAOYSA-N tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCC(CO)CC1 CTEDVGRUGMPBHE-UHFFFAOYSA-N 0.000 description 1
- RXNQBVRCZIYUJK-UHFFFAOYSA-N tert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCC(COS(C)(=O)=O)CC1 RXNQBVRCZIYUJK-UHFFFAOYSA-N 0.000 description 1
- UJCMPIUPGRHLMQ-UHFFFAOYSA-N tert-butyl 4-[2-(2-bromo-4-nitrophenoxy)ethyl]piperidine-1-carboxylate Chemical compound BrC1=C(OCCC2CCN(CC2)C(=O)OC(C)(C)C)C=CC(=C1)[N+](=O)[O-] UJCMPIUPGRHLMQ-UHFFFAOYSA-N 0.000 description 1
- NLSHFDZSIYOALM-UHFFFAOYSA-N tert-butyl 4-[[4-[(1-methoxy-2-methyl-1-oxopropan-2-yl)amino]phenoxy]methyl]piperidine-1-carboxylate Chemical compound COC(C(C)(C)NC1=CC=C(OCC2CCN(CC2)C(=O)OC(C)(C)C)C=C1)=O NLSHFDZSIYOALM-UHFFFAOYSA-N 0.000 description 1
- GXDZRILQELSANI-UHFFFAOYSA-N tert-butyl N-(3-cyano-5-nitrophenyl)carbamate Chemical compound C(#N)C=1C=C(C=C(C=1)[N+](=O)[O-])NC(OC(C)(C)C)=O GXDZRILQELSANI-UHFFFAOYSA-N 0.000 description 1
- IEUIEMIRUXSXCL-UHFFFAOYSA-N tert-butyl n-(3-aminophenyl)carbamate Chemical compound CC(C)(C)OC(=O)NC1=CC=CC(N)=C1 IEUIEMIRUXSXCL-UHFFFAOYSA-N 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000005888 tetrahydroindolyl group Chemical group 0.000 description 1
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 125000004305 thiazinyl group Chemical group S1NC(=CC=C1)* 0.000 description 1
- 125000002769 thiazolinyl group Chemical group 0.000 description 1
- 125000000858 thiocyanato group Chemical group *SC#N 0.000 description 1
- 238000011200 topical administration Methods 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000013518 transcription Methods 0.000 description 1
- 230000035897 transcription Effects 0.000 description 1
- 125000004306 triazinyl group Chemical group 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1
- DTQVDTLACAAQTR-UHFFFAOYSA-N trifluoroacetic acid Substances OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 229910052722 tritium Inorganic materials 0.000 description 1
- 230000004614 tumor growth Effects 0.000 description 1
- 238000007492 two-way ANOVA Methods 0.000 description 1
- 229960005486 vaccine Drugs 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000001262 western blot Methods 0.000 description 1
- 238000005550 wet granulation Methods 0.000 description 1
- 239000003871 white petrolatum Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- GTLDTDOJJJZVBW-UHFFFAOYSA-N zinc cyanide Chemical compound [Zn+2].N#[C-].N#[C-] GTLDTDOJJJZVBW-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/92—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with a hetero atom directly attached to the ring nitrogen atom
- C07D211/94—Oxygen atom, e.g. piperidine N-oxide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/92—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with a hetero atom directly attached to the ring nitrogen atom
- C07D211/98—Nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/28—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/30—Oxygen or sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/86—Oxygen and sulfur atoms, e.g. thiohydantoin
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
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Abstract
Description
本出願は、2018年12月19日に出願された米国仮出願第62/782,281号、及び2019年7月29日に出願された米国仮出願第62/879,927号の利益を主張し、このそれぞれの開示は参照によりその全体が本明細書に組み込まれる。
本明細書では、ある特定の3-((3-アミノフェニル)アミノ)ピペリジン-2,6-ジオン化合物、有効量のかかる化合物を含む組成物、及びアンドロゲン受容体媒介性疾患を治療するまたは予防するための方法を提供し、本方法は、有効量のかかる3-((3-アミノフェニル)アミノ)ピペリジン-2,6-ジオン化合物を、それを必要とする対象に投与することを含む。また本明細書では、これらの方法において使用するための化合物及び組成物も提供する。
を有する化合物、またはその医薬的に許容可能な塩、互変異性体、アイソトポログ、もしくは立体異性体を提供し、式中、RN、R1、R2、R3、R4、X、L、V、m及びnは、本明細書において定義する通りである。
本明細書で使用する場合、「含む(comprising)」及び「含む(including)」という用語は、互換可能に使用することができる。「含む(comprising)」及び「含む(including)」という用語は、記載した特徴または成分の存在を参照されるように指定することとして解釈されるが、1つまたは複数の特徴もしくは成分またはその群の存在または追加を妨げるものではない。加えて、「含む(comprising)」及び「含む(including)」という用語は、「からなる」という用語によって包含される例を含むことが意図される。その結果、「からなる」という用語は、本発明のより特定の実施形態を提供するために、「含む(comprising)」及び「含む(including)」という用語の代わりに使用することができる。
-N(アルキル)C(O)NH(R#)、-N(アルキル)C(O)NH2、-NHC(O)N(R#)2、-NHC(O)NH(R#)、または-NH(CO)NH2のラジカルであり、式中、各アルキル及びR#は、独立して、上で定義される通りである。
本明細書では、以下の式(I):
を有する化合物、またはその医薬的に許容可能な塩、互変異性体、アイソトポログ、もしくは立体異性体を本明細書に提供し、
式中、
RNは、Hであり、
各R1は、独立して、ハロゲン、CN、及びC1-3アルキルから選択され、
R2及びR3は、それぞれ独立して、H、及びC1-3アルキルから選択されるか、またはR2及びR3ならびにそれらが付着している炭素は、置換もしくは不置換C3-6シクロアルキルを形成し、
各R4は、独立して、置換もしくは不置換C1-3アルキル、及びハロゲンから選択されるか、または2つのR4基は、それらが付着している同じ炭素原子もしくは隣接炭素原子と一緒に、置換もしくは不置換C3-6シクロアルキルを形成するか、または2つのR4基は、それらが付着している非隣接炭素原子と一緒に、置換もしくは不置換4~7員ヘテロシクリルを形成し、
Xは、CRxであり、
Rxは、H、ハロゲン、または置換もしくは不置換C1-3アルキルであり、
Lは、-O-、-O(CH2)p-または-(CH2)p-であり、
nは、0~4であり、
mは、0~8であり、
pは、1~3であり、
Vは、
Aは、N、CH、またはCRAであり、
Bは、N、CHまたはCRBであり、
各RAは、独立して、ハロゲン、置換または不置換C1-6アルキル、ならびに置換及び不置換C3-6シクロアルキルから選択され、
各RBは、独立して、ハロゲン、及び置換または不置換C1-6アルキルから選択され、
RCは、ハロゲンまたはCF3であり、
R5及びR6は、C1-3アルキルであるか、またはR5及びR6は、それらが付着している炭素原子と一緒に、置換もしくは不置換C3-5シクロアルキルもしくは3~5員ヘテロシクリルを形成し、
aは、0~3であり、ならびに
bは、0~2である。
RNは、Hであり、
各R1は、独立して、Cl、F、Br、CN、-CH3、及び-CH2CH3から選択され、
R2及びR3は、それぞれ独立して、H、置換もしくは不置換メチル、及びエチルから選択されるか、またはR2及びR3ならびにそれらが付着している炭素は、置換もしくは不置換シクロプロピル、シクロブチルもしくはシクロペンチルを形成し、
各R4は、独立して、置換もしくは不置換メチル及びエチルから選択されるか、または2つのR4基は、それらが付着している同じ炭素原子と一緒に、置換もしくは不置換シクロプロピルもしくはシクロブチルを形成し、
Xは、CRxであり、
Rxは、H、F、またはCH3であり、
Lは、-O-、-O(CH2)p-または-(CH2)p-であり、
nは、0~4であり、
mは、0~8であり、
pは、1~3であり、
Vは、
式中、
Aは、N、CH、またはCRAであり、
Bは、N、CHまたはCRBであり、
各RAは、独立して、Cl、Br、F、メチル、エチル、n-プロピル、イソプロピル、n-ブチル、イソブチル、sec-ブチル、tert-ブチル、n-ペンチル、CH2CH2CH(CH3)2、CH(CH3)CH(CH3)2、CH2C(CH3)3、CF3、CF2CH3、CH2CH2F、CH2CHF2、CH2CF3、CH2OH、CH(CH3)OH、CH2CH2OH、CH(CH3)CH2OH、CH2CH(CH3)OH、シクロプロピル、シクロブチル、及びシクロペンチルから選択され、
各RBは、独立して、ハロゲン、及びメチルから選択され、
RCは、ハロゲンまたはCF3であり、
R5及びR6は、メチルであるか、またはR5及びR6は、それらが付着している炭素原子と一緒に、シクロプロピル、シクロブチル、テトラヒドロフラニル、もしくはテトラヒドロピラニルを形成し、
aは、0~3であり、ならびに
bは、0~2である。
RNは、Hであり、
各R1は、独立して、Cl、F、Br、CN、-CH3、及び-CH2CH3から選択され、
R2及びR3は、それぞれ独立して、H、置換もしくは不置換メチル、及びエチルから選択されるか、またはR2及びR3ならびにそれらが付着している炭素は、置換もしくは不置換シクロプロピル、シクロブチルもしくはシクロペンチルを形成し、
各R4は、独立して、置換もしくは不置換メチル及びエチルから選択されるか、または2つのR4基は、それらが付着している同じ炭素原子と一緒に、置換もしくは不置換シクロプロピルもしくはシクロブチルを形成し、
Xは、CRxであり、
Rxは、H、F、またはCH3であり、
Lは、-O-、-O(CH2)p-または-(CH2)p-であり、
nは、0~4であり、
mは、0~8であり、
pは、1~3であり、
Vは、
式中、
Aは、N、CH、またはCRAであり、
Bは、N、CHまたはCRBであり、
各RAは、独立して、Cl、Br、F、メチル、エチル、n-プロピル、イソプロピル、n-ブチル、イソブチル、sec-ブチル、tert-ブチル、n-ペンチル、CH2CH2CH(CH3)2、CH(CH3)CH(CH3)2、CH2C(CH3)3、CF3、CF2CH3、CH2CH2F、CH2CHF2、CH2CF3、CH2OH、CH(CH3)OH、CH2CH2OH、CH(CH3)CH2OH、CH2CH(CH3)OH、シクロプロピル、シクロブチル、及びシクロペンチルから選択され、
各RBは、独立して、ハロゲン、及びメチルから選択され、
RCは、ハロゲンまたはCF3であり、
R5及びR6は、メチルであるか、またはR5及びR6は、それらが付着している炭素原子と一緒に、シクロプロピル、シクロブチル、テトラヒドロフラニル、もしくはテトラヒドロピラニルを形成し、
aは、0~3であり、ならびに
bは、0~2である。
本明細書に記載するピペリジンジオン化合物は、従来の有機合成及び市販されている出発材料、または本明細書に提供する方法を使用して作成することができる。例として限定するものではないが、式(I)、(式中、RN、R1、R2、R3、R4、R5、R6、RA、RB、Rc、L、V、X、n、m、p、a及びbは、本明細書に定義する通りである)のピペリジンジオン化合物は、下に示すスキーム1から6に、ならびに本明細書に記載する実施例に概説する通りに調製することができる。例示的スキーム及び実施例において記載される手順を改変して、所望の生成物にどのように到達するかは、当業者に公知であり得ることに留意されるものとする。
す。
RNは、Hであり、
各R1は、独立して、ハロゲン、CN、及びC1-3アルキルから選択され、
R2及びR3は、それぞれ独立して、H、及びC1-3アルキルから選択されるか、またはR2及びR3ならびにそれらが付着している炭素は、置換もしくは不置換C3-6シクロアルキルを形成し、
各R4は、独立して、置換もしくは不置換C1-3アルキル、及びハロゲンから選択されるか、または2つのR4基は、それらが付着している同じ炭素原子もしくは隣接炭素原子と一緒に、置換もしくは不置換C3-6シクロアルキルを形成するか、または2つのR4基は、それらが付着している非隣接炭素原子と一緒に、置換もしくは不置換4~7員ヘテロシクリルを形成し、
Xは、CRxであり、
Rxは、H、ハロゲン、または置換もしくは不置換C1-3アルキルであり、
Lは、-O-、-O(CH2)p-または-(CH2)p-であり、
nは、0~4であり、
mは、0~8であり、
pは、1~3であり、
Vは、
Aは、N、CH、またはCRAであり、
Bは、N、CHまたはCRBであり、
各RAは、独立して、ハロゲン、置換もしくは不置換C1-6アルキル、または置換及び不置換C3-6シクロアルキルから選択され、
各RBは、独立して、ハロゲン、及び置換または不置換C1-6アルキルから選択され、
RCは、ハロゲンまたはCF3であり、
R5及びR6は、C1-3アルキルであるか、またはR5及びR6は、それらが付着している炭素原子と一緒に、置換もしくは不置換C3-5シクロアルキルもしくは3~5員ヘテロシクリルを形成し、
aは、0~3であり、ならびに
bは、0~2である。
RNは、Hであり、
各R1は、独立して、ハロゲン、CN、及びC1-3アルキルから選択され、
R2及びR3は、それぞれ独立して、H、及びC1-3アルキルから選択されるか、またはR2及びR3ならびにそれらが付着している炭素は、置換もしくは不置換C3-6シクロアルキルを形成し、
各R4は、独立して、置換もしくは不置換C1-3アルキル、及びハロゲンから選択されるか、または2つのR4基は、それらが付着している同じ炭素原子もしくは隣接炭素原子と一緒に、置換もしくは不置換C3-6シクロアルキルを形成するか、または2つのR4基は、それらが付着している非隣接炭素原子と一緒に、置換もしくは不置換4~7員ヘテロシクリルを形成し、
Xは、CRxであり、
Rxは、H、ハロゲン、または置換もしくは不置換C1-3アルキルであり、
Lは、-O-、-O(CH2)p-または-(CH2)p-であり、
nは、0~4であり、
mは、0~8であり、
pは、1~3であり、
Vは、
Aは、N、CH、またはCRAであり、
Bは、N、CHまたはCRBであり、
各RAは、独立して、ハロゲン、置換もしくは不置換C1-6アルキル、または置換及び不置換C3-6シクロアルキルから選択され、
各RBは、独立して、ハロゲン、及び置換または不置換C1-6アルキルから選択され、
RCは、ハロゲンまたはCF3であり、
R5及びR6は、C1-3アルキルであるか、またはR5及びR6は、それらが付着している炭素原子と一緒に、置換もしくは不置換C3-5シクロアルキルもしくは3~5員ヘテロシクリルを形成し、
aは、0~3であり、ならびに
bは、0~2である。
Aは、N、CH、またはCRAであり、
Bは、N、CH、またはCRBであり、
各RAは、独立して、ハロゲン、置換または不置換C1-6アルキル、及び置換または不置換C3-6シクロアルキルから選択され、
各RBは、独立して、ハロゲン、及び置換または不置換C1-6アルキルから選択され、
RCは、ハロゲンまたはCF3であり、
R5及びR6は、C1-3アルキルであるか、またはR5及びR6は、それらが付着している炭素原子と一緒に、置換もしくは不置換C3-6シクロアルキルもしくは3~6員ヘテロシクリルを形成し、
aは、0~3であり、
bは、0~2である
Xは、CRxであり、
Rxは、H、ハロゲン、または置換もしくは不置換C1-3アルキルであり、
Lは、-O-、-O(CH2)p-または-(CH2)p-であり、
mは、0~8であり、
pは、1~3であり、
各R4は、独立して、置換もしくは不置換C1-3アルキルであるか、または2つのR4基は、それらが付着している同じ炭素原子もしくは隣接炭素原子と一緒に、置換もしくは不置換C3-6シクロアルキルを形成するか、または2つのR4基は、それらが付着している非隣接炭素原子と一緒に、置換もしくは不置換4~7員ヘテロシクリルを形成し、ならびに
PNは、アミン保護基である。
Aは、N、CH、またはCRAであり、
Bは、N、CH、またはCRBであり、
各RAは、独立して、ハロゲン、置換または不置換C1-6アルキル、及び置換または不置換C3-6シクロアルキルから選択され、
各RBは、独立して、ハロゲン、及び置換または不置換C1-6アルキルから選択され、
RCは、ハロゲンまたはCF3であり、
R5及びR6は、C1-3アルキルであるか、またはR5及びR6は、それらが付着している炭素原子と一緒に、置換もしくは不置換C3-6シクロアルキルもしくは3~6員ヘテロシクリルを形成し、
aは、0~3であり、
bは、0~2である
Xは、CRxであり、
Rxは、H、ハロゲン、または置換もしくは不置換C1-3アルキルであり、
Lは、-O-、-O(CH2)p-または-(CH2)p-であり、
mは、0~8であり、
pは、1~3であり、ならびに
各R4は、独立して、置換もしくは不置換C1-3アルキルであるか、または2つのR4基は、それらが付着している同じ炭素原子もしくは隣接炭素原子と一緒に、置換もしくは不置換C3-6シクロアルキルを形成するか、または2つのR4基は、それらが付着している非隣接炭素原子と一緒に、置換もしくは不置換4~7員ヘテロシクリルを形成する。
Aは、N、CH、またはCRAであり、
Bは、N、CH、またはCRBであり、
各RAは、独立して、ハロゲン、置換または不置換C1-6アルキル、及び置換または不置換C3-6シクロアルキルから選択され、
各RBは、独立して、ハロゲン、及び置換または不置換C1-6アルキルから選択され、
RCは、ハロゲンまたはCF3であり、
R5及びR6は、C1-3アルキルであるか、またはR5及びR6は、それらが付着している炭素原子と一緒に、置換もしくは不置換C3-6シクロアルキルもしくは3~6員ヘテロシクリルを形成し、
aは、0~3であり、
bは、0~2であり、
Xは、CRxであり、
Rxは、H、ハロゲン、または置換もしくは不置換C1-3アルキルであり、
Lは、-O-、-O(CH2)p-または-(CH2)p-であり、
mは、0~8であり、
pは、1~3であり、
各R4は、独立して、置換もしくは不置換C1-3アルキルであるか、または2つのR4基は、それらが付着している同じ炭素原子もしくは隣接炭素原子と一緒に、置換もしくは不置換C3-6シクロアルキルを形成するか、または2つのR4基は、それらが付着している非隣接炭素原子と一緒に、置換もしくは不置換4~7員ヘテロシクリルを形成し、
R2及びR3は、それぞれ独立して、H、及びC1-3アルキルから選択されるか、またはR2及びR3ならびにそれらが付着している炭素は、置換もしくは不置換C3-6シクロアルキルを形成し、ならびに
Rは、C1-4アルキルである。
Aは、N、CH、またはCRAであり、
Bは、N、CH、またはCRBであり、
各RAは、独立して、ハロゲン、置換または不置換C1-6アルキル、及び置換または不置換C3-6シクロアルキルから選択され、
各RBは、独立して、ハロゲン、及び置換または不置換C1-6アルキルから選択され、
RCは、ハロゲンまたはCF3であり、
R5及びR6は、C1-3アルキルであるか、またはR5及びR6は、それらが付着している炭素原子と一緒に、置換もしくは不置換C3-6シクロアルキルもしくは3~6員ヘテロシクリルを形成し、
aは、0~3であり、
bは、0~2であり、
Xは、CRxであり、
Rxは、H、ハロゲン、または置換もしくは不置換C1-3アルキルであり、
Lは、-O-、-O(CH2)p-または-(CH2)p-であり、
mは、0~8であり、
pは、1~3であり、
各R4は、独立して、置換もしくは不置換C1-3アルキルであるか、または2つのR4基は、それらが付着している同じ炭素原子もしくは隣接炭素原子と一緒に、置換もしくは不置換C3-6シクロアルキルを形成するか、または2つのR4基は、それらが付着している非隣接炭素原子と一緒に、置換もしくは不置換4~7員ヘテロシクリルを形成し、ならびに
R2及びR3は、それぞれ独立して、H、及びC1-3アルキルから選択されるか、またはR2及びR3ならびにそれらが付着している炭素は、置換もしくは不置換C3-6シクロアルキルを形成する。
Aは、N、CH、またはCRAであり、
Bは、N、CH、またはCRBであり、
各RBは、独立して、ハロゲン、及び置換または不置換C1-6アルキルから選択され、
RCは、ハロゲンまたはCF3であり、
R5及びR6は、C1-3アルキルであるか、またはR5及びR6は、それらが付着している炭素原子と一緒に、置換もしくは不置換C3-6シクロアルキルもしくは3~6員ヘテロシクリルを形成し、
bは、0~2であり、
Xは、CRxであり、
Rxは、H、ハロゲン、または置換もしくは不置換C1-3アルキルであり、
Lは、-O-、-O(CH2)p-または-(CH2)p-であり、
mは、0~8であり、
pは、1~3であり、
各R4は、独立して、置換もしくは不置換C1-3アルキルであるか、または2つのR4基は、それらが付着している同じ炭素原子もしくは隣接炭素原子と一緒に、置換もしくは不置換C3-6シクロアルキルを形成するか、または2つのR4基は、それらが付着している非隣接炭素原子と一緒に、置換もしくは不置換4~7員ヘテロシクリルを形成し、ならびに
PNは、アミン保護基である。
Aは、N、CH、またはCRAであり、
Bは、N、CH、またはCRBであり、
各RBは、独立して、ハロゲン、及び置換または不置換C1-6アルキルから選択され、
RAは、ハロゲン、置換もしくは不置換C1-6アルキル、または置換もしくは不置換C3-6シクロアルキルであり、
RCは、ハロゲンまたはCF3であり、
R5及びR6は、C1-3アルキルであるか、またはR5及びR6は、それらが付着している炭素原子と一緒に、置換もしくは不置換C3-6シクロアルキルもしくは3~6員ヘテロシクリルを形成し、
bは、0~2である
Xは、CRxであり、
Rxは、H、ハロゲン、または置換もしくは不置換C1-3アルキルであり、
Lは、-O-、-O(CH2)p-または-(CH2)p-であり、
mは、0~8であり、
pは、1~3であり、
各R4は、独立して、置換もしくは不置換C1-3アルキルであるか、または2つのR4基は、それらが付着している同じ炭素原子もしくは隣接炭素原子と一緒に、置換もしくは不置換C3-6シクロアルキルを形成するか、または2つのR4基は、それらが付着している非隣接炭素原子と一緒に、置換もしくは不置換4~7員ヘテロシクリルを形成し、ならびに
PNは、アミン保護基である。
一実施形態では、本明細書に記載する化合物は、動物またはヒトにおける状態を治療、予防、または改善するための医薬品として有用性を有する。本明細書に記載するピペリジンジオン化合物は、動物またはヒトにおける状態を治療、予防、または改善するための医薬品として有用性を有する。従って、下に記載するそれらの疾患の治療または予防を含む、ピペリジンジオン化合物の多くの使用を、本明細書に提供する。一実施形態では、本明細書に提供する方法は、有効量の化合物を、それを必要とする対象に投与することを含む。
本明細書に提供する化合物は、対象に、経口的に、局所的にまたは非経口的に、調製物の従来の形態、例えばカプセル、マイクロカプセル、錠剤、顆粒、粉末、トローチ、丸剤、坐剤、注射、懸濁液、シロップ、パッチ、クリーム、ローション、軟膏、ゲル、噴霧、溶液及びエマルションにて、投与することができる。
実施例1:2-(4-(4-(3-(4-シアノ-3-(トリフルオロメチル)フェニル)-5,5-ジメチル-4-オキソ-2-チオキソイミダゾリジン-1-イル)-2-フルオロフェノキシ)ピペリジン-1-イル)-N-(3-((2,6-ジオキソピペリジン-3-イル)アミノ)フェニル)アセトアミドギ酸塩
細胞ベースのアッセイ
VCAP AR分解アッセイ。試験化合物を、各化合物について1:3希釈にて10点濃度系列を作成するように、アコースティックディスペンサーを使用して、Corning CellBind 96ウェル透明底プレート(カタログ番号3300)に、事前に分注した。各化合物の最終的な最高濃度は、5μMとした。0.1%の最終濃度のDMSOを、対照として使用した。8%ウシ胎児血清(FBS)を伴うDMEMにて培養したVCaP細胞を、ウェルあたり50K個の細胞にて200μlの体積で、化合物プレートに播種し、37℃にてCO2中インキュベーターで24時間インキュベートした。培地を、細胞から注意深く除去し、プレートを氷上に置いた。Cell Signaling Technologiesの100μLの氷冷1×細胞溶解緩衝液(カタログ番号9803)を、細胞の各ウェルに加え、プレートを、4℃にてシェーカー上で1時間インキュベートした。PathScan Total Sandwich AR ELISAキット(Cell Signaling Technology、カタログ番号12580)を使用したAR ELISA検出のために、15μLの細胞溶解物を使用した。化合物で処理したウェルにおけるARレベルを、DMSO対照のレベルに対して正規化し、対照の割合(%)(PoC)(y)として表した。4パラメータロジスティックモデル(シグモイド用量反応モデル)を使用して、化合物のDC50、及びEC50を決定し、これには以下の等式を使用した:
y=(A+((B-A)/(1+((C/x)^D))))
A=YMin(カーブフィットによって決定される、化合物処理に反応したDMSO対照に対して正規化した最低ARレベル)
B=YMax(カーブフィットによって決定される、最大ARレベル)
C=EC50
D=曲線傾き
x=化合物濃度
EC50=yが(YMax-YMin)/2である場合の化合物の濃度
DC50=yがDMSO対照の50%(50%AR分解)である場合の化合物の濃度
y=DMSO対照に対して正規化したARタンパク質レベル
y=(A+((B-A)/(1+((C/x)^D))))
A=YMin(カーブフィットによって決定される、化合物処理に反応したDMSO対照に対して正規化した発光単位での最低細胞生存率)
B=YMax(カーブフィットによって決定される、DMSO対照に対して正規化した発光単位として測定した最大細胞生存率)
C=EC50
D=曲線傾き
GI50=Yが(YMax+Yt0)/2である場合の化合物の濃度
EC50=yが(YMax-YMin)/2である場合の化合物の濃度
IC50=YがDMSO対照の50%である場合の化合物の濃度
y=発光単位として測定し、DMSO対照のパーセンテージとして正規化した細胞生存率
t0=化合物を加えた時間
AR分解アッセイ。インビボAR分解アッセイを、VCaP前立腺癌異種移植腫瘍を有するNSGマウスで行った。雄NSGマウスの右脚の上にある側腹領域に、VCaP細胞を接種した。動物の接種後、腫瘍を、およそ500mm3まで成長させてから、無作為化した。無作為化された動物に、20%ラブラソル、80%25mMクエン酸緩衝液pH3中で製剤化された試験化合物を投与した。化合物を、1日1回、3日間経口投与した。化合物投与の最後の用量後、血漿及び腫瘍を収集し、AR分解アッセイのために処理した。腫瘍内ARレベルを、ウエスタンブロット分析を使用して測定した。統計分析を、一元配置分散分析(ANOVA)を使用して行った。
表1のピペリジンジオン化合物をそれぞれ、上に示したAR分解アッセイのうちの1つまたは複数、例えば、VCAP AR分解アッセイアッセイにおいて試験し、そこで活性を有することが見出された。
Claims (40)
- 式(I)
式中、
RNが、Hであり、
各R1が、独立して、ハロゲン、CN、及びC1-3アルキルから選択され、
R2及びR3が、それぞれ独立して、H、及びC1-3アルキルから選択されるか、またはR2及びR3ならびにそれらが付着している炭素が、置換もしくは不置換C3-6シクロアルキルを形成し、
各R4が、独立して、置換もしくは不置換C1-3アルキル、及びハロゲンから選択されるか、または2つのR4基が、それらが付着している同じ炭素原子もしくは隣接炭素原子と一緒に、置換もしくは不置換C3-6シクロアルキルを形成するか、または2つのR4基が、それらが付着している非隣接炭素原子と一緒に、置換もしくは不置換4~7員ヘテロシクリルを形成し、
Xが、CRxであり、
Rxが、H、ハロゲン、または置換もしくは不置換C1-3アルキルであり、
Lが、-O-、-O(CH2)p-または-(CH2)p-であり、
nが、0~4であり、
mが、0~8であり、
pが、1~3であり、
Vが、
Aが、N、CH、またはCRAであり、
Bが、N、CHまたはCRBであり、
各RAが、独立して、ハロゲン、置換または不置換C1-6アルキル、ならびに置換及び不置換C3-6シクロアルキルから選択され、
各RBが、独立して、ハロゲン、及び置換または不置換C1-6アルキルから選択され、
RCが、ハロゲンまたはCF3であり、
R5及びR6が、C1-3アルキルであるか、またはR5及びR6が、それらが付着している炭素原子と一緒に、置換もしくは不置換C3-5シクロアルキルもしくは3~5員ヘテロシクリルを形成し、
aが、0~3であり、ならびに
bが、0~2である、前記化合物またはその医薬的に許容可能な塩、互変異性体、アイソトポログ、もしくは立体異性体。 - 各R1が、独立して、Cl、F、Br、CN、-CH3、及び-CH2CH3から選択される、請求項1に記載の化合物。
- 各R1が、独立して、Cl、F、及びCNから選択される、請求項1に記載の化合物。
- nが、0である、請求項1に記載の化合物。
- nが、1である、請求項1に記載の化合物。
- R2及びR3が、それぞれ独立して、H、置換もしくは不置換メチル、及びエチルから選択されるか、またはR2及びR3ならびにそれらが付着している炭素が、置換もしくは不置換シクロプロピル、シクロブチルもしくはシクロペンチルを形成する、請求項1に記載の化合物。
- R2及びR3が、それぞれ独立して、H及びメチルから選択されるか、またはR2及びR3ならびにそれらが付着している炭素が、不置換シクロプロピルを形成する、請求項1に記載の化合物。
- R2及びR3が、両方ともHもしくはメチルであるか、またはR2及びR3ならびにそれらが付着している炭素が、不置換シクロプロピルを形成する、請求項1に記載の化合物。
- 各R4が、独立して、置換もしくは不置換メチル及びエチルから選択されるか、または2つのR4基が、それらが付着している同じ炭素原子と一緒に、置換もしくは不置換シクロプロピルもしくはシクロブチルを形成する、請求項1に記載の化合物。
- 各R4が、独立して、置換もしくは不置換メチルから選択されるか、または2つのR4基が、それらが付着している同じ炭素原子と一緒に、不置換シクロプロピルを形成する、請求項1に記載の化合物。
- 各R4が、独立して、メチル及びCH2OHから選択されるか、または2つのR4基が、それらが付着している同じ炭素原子と一緒に、不置換シクロプロピルを形成する、請求項1に記載の化合物。
- mが、0、1、2、3または4である、請求項1に記載の化合物。
- mが、0、1、または2である、請求項1に記載の化合物。
- 2つのR4基が、それらが付着している非隣接炭素原子と一緒に、不置換4~7員ヘテロシクリルを形成する、請求項1に記載の化合物。
- Rxが、Hである、請求項1に記載の化合物。
- Rxが、CH3である、請求項1に記載の化合物。
- Rxが、Fである、請求項1に記載の化合物。
- Lが、-O-、-O(CH2)-、または-O(CH2)(CH2)-である、請求項1に記載の化合物。
- Aが、CHである、請求項1に記載の化合物。
- Bが、CHである、請求項1に記載の化合物。
- Bが、Nである、請求項1に記載の化合物。
- aが、0、1または2である、請求項1に記載の化合物。
- 各RAが、独立して、Cl、Br、F、メチル、エチル、n-プロピル、イソプロピル、n-ブチル、イソブチル、sec-ブチル、tert-ブチル、n-ペンチル、CH2CH2CH(CH3)2、CH(CH3)CH(CH3)2、CH2C(CH3)3、CF3、CF2CH3、CH2CH2F、CH2CHF2、CH2CF3、CH2OH、CH(CH3)OH、CH2CH2OH、CH(CH3)CH2OH、CH2CH(CH3)OH、シクロプロピル、シクロブチル、及びシクロペンチルから選択される、請求項19に記載の化合物。
- 各RAが、独立して、Cl、F、エチル、イソプロピル、CF2CH3、及びCH2CH2Fから選択される、請求項1に記載の化合物。
- 各RAが、独立して、Cl、F、エチル、イソプロピル、CF2CH3、及びCH2CH2Fから選択される、請求項20に記載の化合物。
- 各RAが、独立して、Cl、エチル、イソプロピル、CF2CH3及びCH2CH2Fから選択される、請求項21に記載の化合物。
- bが、0である、請求項1に記載の化合物。
- RCが、CF3である、請求項1に記載の化合物。
- R5及びR6が、メチルであるか、またはR5及びR6が、それらが付着している炭素原子と一緒に、シクロプロピル、シクロブチル、テトラヒドロフラニル、もしくはテトラヒドロピラニルを形成する、請求項1に記載の化合物。
- R5及びR6が、メチルであるか、またはR5及びR6が、それらが付着している炭素原子と一緒に、シクロブチルを形成する、請求項1に記載の化合物。
- 表1からの化合物。
- 有効量の請求項1~31のいずれか1項に記載の化合物、またはその医薬的に許容可能な塩、互変異性体、同位体置換体、もしくは立体異性体、及び医薬的に許容可能な担体、賦形剤またはビヒクルを含む、医薬組成物。
- アンドロゲン受容体媒介性疾患の治療のための方法であって、有効量の請求項1~31のいずれか1項に記載の化合物を、それを必要とする対象に投与することを含む、前記方法。
- アンドロゲン受容体媒介性疾患を治療するための方法であって、有効量の請求項32に記載の医薬組成物を、それを必要とする対象に投与することを含む、前記方法。
- 前記アンドロゲン媒介性疾患が、前立腺癌である、請求項33または34に記載の方法。
- 前記前立腺癌が、去勢抵抗性前立腺癌(CRPC)である、請求項35に記載の方法。
- アンドロゲン受容体媒介性疾患の前記治療のための方法において使用するための、請求項1~31のいずれか1項に記載の化合物。
- アンドロゲン受容体媒介性疾患の前記治療のための方法において使用するための、請求項32に記載の医薬組成物。
- 前記アンドロゲン媒介性疾患が、前立腺癌である、請求項37に記載の使用するための化合物または請求項38に記載の使用するための医薬組成物。
- 前記前立腺癌が、去勢抵抗性前立腺癌(CRPC)である、請求項39に記載の使用するための化合物または医薬組成物。
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