JP2007516290A - 肥満およびcns障害の処置のための選択的d1ドーパミンレセプターアンタゴニストとしての置換n−アリールアミジン - Google Patents

肥満およびcns障害の処置のための選択的d1ドーパミンレセプターアンタゴニストとしての置換n−アリールアミジン Download PDF

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JP2007516290A
JP2007516290A JP2006547263A JP2006547263A JP2007516290A JP 2007516290 A JP2007516290 A JP 2007516290A JP 2006547263 A JP2006547263 A JP 2006547263A JP 2006547263 A JP2006547263 A JP 2006547263A JP 2007516290 A JP2007516290 A JP 2007516290A
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alkyl
compound
aryl
group
hydrogen
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JP2007516290A5 (enExample
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デュアン エー. バーネット,
ウェン−リエン ウー,
マーティン エス. ドマルスキー,
メアリー アン カプレン,
リチャード スプリング,
ジーン イー. ラチョウィクツ,
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Merck Sharp and Dohme LLC
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Schering Corp
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    • C07D295/16Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/20Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
    • C07D295/205Radicals derived from carbonic acid
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    • C07C257/14Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines having carbon atoms of amidino groups bound to acyclic carbon atoms
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JP2006547263A 2003-12-23 2004-12-21 肥満およびcns障害の処置のための選択的d1ドーパミンレセプターアンタゴニストとしての置換n−アリールアミジン Pending JP2007516290A (ja)

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US53224103P 2003-12-23 2003-12-23
PCT/US2004/042934 WO2005063697A2 (en) 2003-12-23 2004-12-21 Substituted n-aryl amidines as selective d1 dopamine receptor antagonists for the treatment of obesity and cns disorders

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JP2007516290A5 JP2007516290A5 (enExample) 2008-02-07

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US (1) US7423149B2 (enExample)
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US20100105682A1 (en) * 2006-10-13 2010-04-29 Hassan Pajouhesh Cyclopropyl-piperazine compounds as calcium channel blockers
CN110437106B (zh) * 2019-06-27 2021-09-07 广东药科大学 芳基脒类化合物及其合成方法
CN111233744B (zh) * 2020-02-26 2021-09-17 陕西科技大学 (e)1-氰基-1-取代-2-(9-烷基-咔唑-3-)基-乙烯及其制备方法

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JPS59157069A (ja) * 1983-02-18 1984-09-06 ビ−チヤム・グル−プ・ピ−エルシ− アミジン化合物
WO1995008533A1 (en) * 1993-09-21 1995-03-30 Yamanouchi Pharmaceutical Co., Ltd. N-(3-pyrrolidinyl)benzamide derivative
JPH10501819A (ja) * 1994-09-27 1998-02-17 ニューロゲン コーポレイション ある種のアミノメチルフェニルイミダゾール誘導体:新しいクラスのドーパミン受容体サブタイプ特異的リガンド
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