JP2016509051A - キナーゼ阻害剤としてのキナゾリン類 - Google Patents
キナーゼ阻害剤としてのキナゾリン類 Download PDFInfo
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- JP2016509051A JP2016509051A JP2015558582A JP2015558582A JP2016509051A JP 2016509051 A JP2016509051 A JP 2016509051A JP 2015558582 A JP2015558582 A JP 2015558582A JP 2015558582 A JP2015558582 A JP 2015558582A JP 2016509051 A JP2016509051 A JP 2016509051A
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Abstract
Description
式:
式:
式
本発明の化合物は、以下のスキームに示される合成手順を用いて、または熟練の有機化学者の知識に頼ることによって得ることができる。これらのスキームに示される合成は、必要であれば本明細書で概略を示す反応との適合性を達成するために適宜保護された適当な前駆体を用いて、種々の異なる置換基を有する本発明の化合物を生産するために適用可能である。要すれば、その後の脱保護により、一般に開示されている性質の化合物が得られる。スキームが一般式のみの化合物で示される場合、それらは本発明の化合物を製造するために使用可能なプロセスの例示である。
6−ブロモ−7−フルオロキナゾリン−4−オール(69g、285mmol)、テトラキス(トリフェニルホスフィン)−パラジウム(0)(20g、17mmol)および炭酸ナトリウム(60g、570mmol)の混合物を、窒素ガスでパージしながら5分間、DMF(1L)中で撹拌した。2−メチルプロパン−2−チオール(64ml、570mmol)を加え、この反応混合物を還流冷却器下、100℃で6時間加熱した。この反応物を冷却し、ガラスフィルターペーパーで濾過した後、撹拌している1500mlの水中にゆっくり注いだ。得られた赤色沈澱を濾過し、200mLのEtOAcで摩砕した。固体を濾過し、110mlのヘキサン、150mlの90:10ヘキサン:EtOAcで順次洗浄し、6−(tert−ブチルチオ)−7−フルオロキナゾリン−4−オール(44.5g、収率61.9%)を黄褐色固体として得た。LC/MS: M+H = 253.2 1H NMR (400 MHz, DMSO-d6) δ ppm 12.23 - 12.72 (m, 1 H), 8.24 (d, J=8.1 Hz, 1 H), 8.19 (s, 1 H), 7.58 (d, J=9.6 Hz, 1 H), 1.28 (s, 9 H)。
酢酸エチル(1220ml)、メタノール(1220ml)、および水(1220ml)中、6−(tert−ブチルチオ)−7−フルオロキナゾリン−4−オール(45g、124mmol)およびオキソン(191g、311mmol)の懸濁液を、25℃で4時間撹拌し、この時、25g(合計2.8当量)のオキソンを追加した。この反応混合物を12時間オーバーヘッドスターラーにより撹拌した。この反応物を濾過し、濾液を飽和重炭酸ナトリウム水溶液、次いで固体重炭酸ナトリウムでゆっくり塩基性としてpH約7.5とした。この混合物をさらに1.25LのEtOAc、次いで500mlのEtOAcで抽出した。合わせた有機液をブラインで洗浄した後、MgSO4で乾燥させ、濾過し、真空濃縮した。少量の不純物を、200mlのEtOAcで摩砕することにより除去した。目的の6−(tert−ブチルスルホニル)−7−フルオロキナゾリン−4−オール(33.2g、収率94%)を黄色固体として濾取した。LC/MS: M+H = 285.2 1H NMR (400 MHz, DMSO-d6) δ ppm 12.48 - 13.03 (m, br. s, 1 H), 8.47 (d, J=7.8 Hz, 1 H), 8.32 (s, 1 H), 7.73 (d, J=11.1 Hz, 1 H), 1.17 - 1.40 (s, 9 H)。
アセトニトリル(48ml)中、6−(tert−ブチルスルホニル)−7−フルオロキナゾリン−4−オール(5.50g、19.35mmol)の懸濁液に、POCl3(2.70ml、29.0mmol)およびTEA(4.0ml、29mmol)を加えた。この反応混合物を80℃で一晩撹拌した。この溶液に4,5−ジメチル−1H−ピラゾール−3−アミン(2.58g、23.2mmol)を加え、この反応混合物を80℃で1時間撹拌した。固体が析出し始めた。この反応混合物を室温まで冷却した。固体を濾過し、冷アセトニトリルで洗浄した。固体を真空炉で乾燥させて、6−(tert−ブチルスルホニル)−N−(4,5−ジメチル−1H−ピラゾール−3−イル)−7−フルオロキナゾリン−4−アミン塩酸塩(4.91g、11.86mmol、収率61.3%)を得た。(M+H)+ 378.2。
ナトリウムエトキシド(24ml、65.6mmol、EtOH中21%)および6−(tert−ブチルスルホニル)−N−(4,5−ジメチル−1H−ピラゾール−3−イル)−7−フルオロキナゾリン−4−アミン塩酸塩(4.80g、11.60mmol)を合わせ、この懸濁液を80℃で2時間加熱した。この反応混合物を室温まで冷却した。EtOHを蒸発させ、残渣を25mlの水に溶かした。この溶液を、1N HClを加えることによってpH約9に中和した。淡黄色固体が析出した。固体を濾過し、水で洗浄し、真空炉内で一晩乾燥させ、6−(tert−ブチルスルホニル)−N−(4,5−ジメチル−1H−ピラゾール−3−イル)−7−エトキシキナゾリン−4−アミン(3.90g、9.67mmol、収率83%)を得た。(M+H)+ 404.1; 1H NMR (DMSO-d6, 400MHz): δ = 12.20 (s, 1 H), 10.36 (s, 1 H), 8.99 (s, 1 H), 8.46 (s, 1 H), 7.30 (s, 1 H), 4.13 - 4.34 (m, 2 H), 2.18 (s, 3 H), 1.74 (s, 3 H), 1.40 (t, J=6.9 Hz, 3 H), 1.33 ppm (s, 9 H)。
実施例A
錠剤は常法を用いて作製され、次のように処方される。
成分 1錠当たりの量
化合物 5mg
微晶質セルロース 100mg
ラクトース 100mg
グリコール酸ナトリウムデンプン 30mg
ステアリン酸マグネシウム 2mg
総量 237mg
カプセル剤は常法を用いて作製され、次のように処方される。
成分 1錠当たりの量
化合物 15mg
乾燥デンプン 178mg
ステアリン酸マグネシウム 2mg
総量 195mg
RIPK2のATP結合ポケットにおける新規な試験化合物の相互作用を、蛍光標識ATP競合リガンドとの競合により定量するために蛍光偏光に基づく結合アッセイを開発した。バキュロウイルス発現系から全長FLAG Hisタグを有するRIPK2を精製し、KDapparentの2倍の最終アッセイ濃度で用いた。蛍光標識リガンド(5−({[2−({[3−({4−[(5−ヒドロキシ−2−メチルフェニル)アミノ]−2−ピリミジニル}アミノ)フェニル]カルボニル}アミノ)エチル]アミノ}カルボニル)−2−(6−ヒドロキシ−3−オキソ−3H−キサンテン−9−イル)安息香酸、WO2011/120025に記載のように製造)を5nMの最終アッセイ濃度で用いた。酵素およびリガンドの両方を、50mM HEPES pH7.5、150mM NaCl、10mM MgCl2、1mM DTT、および1mM CHAPS中の溶液として調製した。試験化合物を100%DMSO中に調製し、100nLをマルチウェルプレートの個々のウェルに分注した。次に、5μlのRIPK2を最終アッセイ濃度の2倍で試験化合物に加え、室温で10分間インキュベートした。インキュベーション後、5μlの蛍光標識リガンド溶液を最終アッセイ濃度の2倍で各反応物に加え、室温で少なくとも10分間インキュベートした。最後に、サンプルを、蛍光偏光を測定することができる装置で読み取った。試験化合物の阻害は、内部アッセイ対照に対する阻害率(%)として表した。
全長ヒトRIPK2(受容体共役セリン−スレオニンキナーゼ2)cDNAを、Invitrogen(カールズッバッド、カリフォルニア州、USA、クローンID:IOH6368、RIPK2−pENTR 221)から購入した。Gateway(商標)LRクローニングを用い、Invitrogenが記載しているプロトコールに従い、指定ベクターpDEST8−FLAG−His6内に含まれているN末端FLAG−6Hisの下流のRIPK2を部位特異的に組み換えた。セルフェクチン(商標)(Invitrogen)を製造者のプロトコールに従って用い、ヨトウガ(Spodoptera frugiperda)(Sf9)昆虫細胞へのトランスフェクションを行った。
新規な試験化合物の細胞効力および有効性を評価するために、ムラミルジペプチド(MDP)刺激ヒト全血サイトカイン産生アッセイを開発した。健常なヒトボランティアから得たヘパリン添加血液(160μL)をマルチウェルプレートの個々のウェルに分注した。試験化合物を100%DMSOに溶かし、カルシウム不含、マグネシウム不含D−PBSで希釈して、10倍検量保存溶液を調製した。20マイクロリットルの希釈試験化合物を各ウェルに加え、これらのプレートをプレートシェーカー(500rpm)上に置き、加湿インキュベーター(37℃、5%CO2)内で30分間インキュベートした。MDPの10倍検量保存溶液を、1%DMSOを含有する無菌の内毒素不含水で調製した。20マイクロリットルのMDP保存溶液を各ウェルに加え(終濃度=100ng/mL)、RIP2キナーゼ依存性サイトカイン産生を刺激した。DMSOの終濃度は総てのウェルで0.1%(v/v)であった。プレートをさらに6時間インキュベートした(上記の通り)。次に、ウェル当たりさらに100μLのD−PBS(ダルベッコのリン酸緩衝生理食塩水)を加え、プレートを遠心分離し、上清を回収した。上清のTNFαレベルを、市販のイムノアッセイ(MesoScale Discovery)を用いて定量した。試験化合物阻害は、内部アッセイ対照に対する阻害率(%)として表した。濃度/用量応答実験では、正規化データを当てはめ、従来の技術を用いてpIC50を求めた。pIC50の平均を採り、最低2回の実験の平均値を求めた。
RIP2阻害剤の有効性はin vivoにおいて齧歯類でも評価することができる。マウスにおけるL18−MDPの腹腔内(i.p.)または静脈内(i.v.)投与は、NOD2シグナル伝達経路の活性化を介して炎症性応答を誘導することが示されている(Rosenweig, H. L., et al. 2008. Journal of Leukocyte Biology 84:529-536)。L18−MDP処置ラットにおける炎症性応答のレベルは、血清および/または腹腔洗浄液中の1種類以上のサイトカインレベル(IL8、TNFα、IL6およびIL−1β)の増加を測定すること、および/または腹腔空間への好中球の流入(L18−MDPが腹腔内投与される場合)を測定することによる従来の技術を用いてモニタリングする。処置されたラットにおけるL18−MDP誘導性の炎症性応答の阻害は、試験化合物を予め経口投与し、その後、従来の技術を用いて血清の1種類以上のサイトカインレベル(IL8、TNFα、IL6およびIL−1β)を測定し、対照処置動物と比較することによって示すことができる。
体重2.2〜3kgの雌のウサギにヘパリンで抗凝固処置を施し、ペントバルビタール(50mg/kg,i.v.)で麻酔した。左開胸術により胸を開き、心臓を摘出し、低温(4℃)の標準タイロード液からなる心停止液に入れた。左心室から幅およそ1.5cm、長さ2〜3cmの寸法の貫壁ウェッジを取った。
実施例2の化合物(6−(tert−ブチルスルホニル)−N−(4,5−ジメチル−1H−ピラゾール−3−イル)−7−エトキシキナゾリン−4−アミン)のキノーム選択性(Reaction Biology Corporation, One Great Valley Parkway, Malvern, PA, USA, 19355, http://www.reactionbiology.comにより実施された通り)を、337メンバーのキナーゼパネルに対するin vitroプロファイリングにより決定した。1μMの濃度で実施例2の化合物は、337の供試キナーゼのうち1つの>70%阻害、そして、337供試キナーゼのうち4つの>50%阻害を示した。
Claims (17)
- 6−(tert−ブチルスルホニル)−N−(4,5−ジメチル−1H−ピラゾール−3−イル)−7−エトキシキナゾリン−4−アミンである化合物。
- 6−(tert−ブチルスルホニル)−N−(4,5−ジメチル−1H−ピラゾール−3−イル)−7−エトキシキナゾリン−4−アミンまたはその薬学的に許容可能な塩である化合物。
- 6−(tert−ブチルスルホニル)−N−(4,5−ジメチル−1H−ピラゾール−3−イル)−7−エトキシキナゾリン−4−アミンまたはその薬学的に許容可能な塩と、1種類以上の薬学的に許容可能な賦形剤とを含んでなる、医薬組成物。
- 6−(tert−ブチルスルホニル)−N−(4,5−ジメチル−1H−ピラゾール−3−イル)−7−エトキシキナゾリン−4−アミンと1種類以上の薬学的に許容可能な賦形剤とを含んでなる、医薬組成物。
- RIP2キナーゼにより媒介される疾患または障害を治療する方法であって、治療上有効な量の、請求項2に記載の化合物またはその薬学的に許容可能な塩を、それを必要とするヒトに投与することを含んでなる、方法。
- RIP2キナーゼにより媒介される疾患または障害を治療する方法であって、治療上有効な量の請求項3に記載の化合物を、それを必要とするヒトに投与することを含んでなる、方法。
- 療法に使用するための、請求項2に記載の化合物またはその薬学的に許容可能な塩。
- 療法に使用するための、請求項3に記載の化合物。
- RIP2キナーゼにより媒介される疾患または障害の治療において使用するための、請求項2に記載の化合物またはその薬学的に許容可能な塩。
- RIP2キナーゼにより媒介される疾患または障害の治療において使用するための、請求項3に記載の化合物。
- RIP2キナーゼにより媒介される疾患または障害の治療のための薬剤の製造における、請求項2に記載の化合物またはその薬学的に許容可能な塩の使用。
- RIP2キナーゼにより媒介される疾患または障害の治療のための薬剤の製造における、請求項3に記載の化合物の使用。
- 前記疾患または障害が、ブドウ膜炎、インターロイキン−1変換酵素関連熱症候群、皮膚炎、急性肺傷害、2型糖尿病、関節炎、関節リウマチ、潰瘍性大腸炎、クローン病、早期発症型炎症性腸疾患、腸管外炎症性腸疾患、固形臓器移植における虚血再潅流傷害の予防、非アルコール性脂肪性肝炎、アルコール性脂肪性肝炎、自己免疫性肝炎、喘息、移植片対宿主病、全身性紅斑性狼瘡、多発性硬化症、サルコイドーシス、ブラウ症候群、早期発症型サルコイドーシス、ウェゲナー肉腫症、および間質性肺疾患から選択される、請求項6または7に記載の方法。
- 前記疾患または障害が、ブドウ膜炎、インターロイキン−1変換酵素関連熱症候群、皮膚炎、急性肺傷害、2型糖尿病、関節炎、関節リウマチ、潰瘍性大腸炎、クローン病、早期発症型炎症性腸疾患、腸管外炎症性腸疾患、固形臓器移植における虚血再潅流傷害の予防、非アルコール性脂肪性肝炎、アルコール性脂肪性肝炎、自己免疫性肝炎、喘息、移植片対宿主病、全身性紅斑性狼瘡、多発性硬化症、サルコイドーシス、ブラウ症候群、早期発症型サルコイドーシス、ウェゲナー肉腫症、および間質性肺疾患から選択される、請求項10または11に記載の化合物またはその薬学的に許容可能な塩。
- 前記疾患または障害が、ブドウ膜炎、インターロイキン−1変換酵素関連熱症候群、ブラウ症候群、早期発症型サルコイドーシス、潰瘍性大腸炎、クローン病、ウェゲナー肉芽腫症およびサルコイドーシスから選択される、請求項6または7に記載の方法。
- 前記疾患または障害が、ブドウ膜炎、インターロイキン−1変換酵素関連熱症候群、ブラウ症候群、早期発症型サルコイドーシス、潰瘍性大腸炎、クローン病、ウェゲナー肉芽腫症およびサルコイドーシスから選択される、請求項10または11に記載の化合物またはその薬学的に許容可能な塩。
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AU2014220300A1 (en) | 2015-08-06 |
JP6301374B2 (ja) | 2018-03-28 |
US20150361069A1 (en) | 2015-12-17 |
AU2014220300B2 (en) | 2016-10-13 |
AR094707A1 (es) | 2015-08-19 |
CN105143208A (zh) | 2015-12-09 |
EP2958911B1 (en) | 2017-10-18 |
CA2902132A1 (en) | 2014-08-28 |
EP2958911A1 (en) | 2015-12-30 |
TW201444824A (zh) | 2014-12-01 |
KR20150118152A (ko) | 2015-10-21 |
WO2014128622A1 (en) | 2014-08-28 |
TWI630203B (zh) | 2018-07-21 |
ES2654100T3 (es) | 2018-02-12 |
RU2662810C2 (ru) | 2018-07-31 |
RU2015139758A (ru) | 2017-03-24 |
CN105143208B (zh) | 2017-09-26 |
US9650364B2 (en) | 2017-05-16 |
BR112015019624A2 (pt) | 2017-07-18 |
CA2902132C (en) | 2020-09-22 |
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