AR055401A1 - Derivados de benzotiazolona - Google Patents

Derivados de benzotiazolona

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Publication number
AR055401A1
AR055401A1 ARP060103747A ARP060103747A AR055401A1 AR 055401 A1 AR055401 A1 AR 055401A1 AR P060103747 A ARP060103747 A AR P060103747A AR P060103747 A ARP060103747 A AR P060103747A AR 055401 A1 AR055401 A1 AR 055401A1
Authority
AR
Argentina
Prior art keywords
alkyl
optionally substituted
ring
independently represent
alkoxycarbonyl
Prior art date
Application number
ARP060103747A
Other languages
English (en)
Inventor
Andrew Bailey
Roger V Bonnert
Steve Connolly
Tony Ingall
Garry Pairaudeau
Michael Stocks
Original Assignee
Astrazeneca Ab
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of AR055401A1 publication Critical patent/AR055401A1/es

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/60Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D277/62Benzothiazoles
    • C07D277/68Benzothiazoles 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 in position 2
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
    • A61K31/428Thiazoles condensed with carbocyclic rings
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Abstract

Reivindicacion 1: Un compuesto caracterizado porque es de formula (1) donde R1 representa H; cada uno de R2, R3, R4, R5, R4' y R5' representa en forma independiente H o alquilo C1-6, x es 0 o 1; A representa O, S, S(O) o S(O)2; D representa O, S o NR6; W es un enlace o CR6aR6b; n es un entero entre 0 y 2; R6 representa H, alquilo C1-6, alcoxicarbonilo C1-6 o aril C1-6-alquilo; Y es un enlace, CR2eR2f o CR2gR2hCR2kR2m; R2a, R2b, R2c, R2d, R2e, R2f, R2g, R2h, R2k, R2m, R6a y R6b son, de forma independiente, H o alquilo C1-6; R7a es H, alquilo C1-6 o NHR7b; R7b es H, alquilo C1-6, alcoxicarbonilo C1-6 o aril C1-6-alquilo; R7 representa un sistema de anillos aromático o heteroaromático de entre 5 y 14 miembros opcionalmente sustituido con halogeno, trifluorometilo, hidroxilo, carboxilo, alquilo C1-6 (opcionalmente sustituido con -NR10R11), alcoxi C1-6 (opcionalmente sustituido con -NR12R13), alcoxicarbonilo C1-6, -NR14R15, alquilcarbonilamino C1-6, alquilsulfonilamino C1-6, fenilsulfonilamino, -C(O)NHR16, -SO2NHR17, alquil C0-6-R18, o un fenilo o anillo heteroaromático de 5 o 6 miembros (donde cada uno de los cuales está opcionalmente sustituido con halogeno, trifluorometilo, hidroxilo, alquilo C1-6, alcoxi C1-6 o - NR21R22); R10, R11, R12, R13, R14 y R15 representan en forma independiente entre sí H o alquilo C1-6; R16 representa , alquilo C1-6, fenil-alquilo C0-6 o alquilen C2-6-NR19R20, R19 y R20 representan en forma independiente entre sí H o alquilo C1-6, o R19 y R20 junto con el átomo de N al cual están unidos forman un anillo heterocíclico saturado de entre 4 y 6 miembros que comprende opcionalmente un heteroátomo del anillo adicional seleccionado entre N y O; R17 representa H, alquilo C1-6, fenil- alquilo C0-6 o alquilen C2-6-NR23R24; R23 y R24 representan en forma independiente entre sí H o alquilo C1-6, o R23 y R24 junto con el átomo de N al cual están nidos forman un anillo heterocíclico saturado de entre 4 y 6 miembros que comprende opcionalmente un heteroátomo del anillo adicional seleccionado entre N y O; R18 representa un anillo saturado que contiene N de 5 o 6 miembros; y R21 y R22 representan en forma independiente entre sí H o alquilo C1-6, o una sal aceptable para uso farmacéutico del mismo.
ARP060103747A 2005-08-29 2006-08-29 Derivados de benzotiazolona AR055401A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE0501905 2005-08-29
SE0601331 2006-06-15

Publications (1)

Publication Number Publication Date
AR055401A1 true AR055401A1 (es) 2007-08-22

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ARP060103747A AR055401A1 (es) 2005-08-29 2006-08-29 Derivados de benzotiazolona

Country Status (15)

Country Link
US (1) US20090221653A1 (es)
EP (1) EP1937656A4 (es)
JP (1) JP2009507788A (es)
KR (1) KR20080038373A (es)
AR (1) AR055401A1 (es)
AU (1) AU2006285448A1 (es)
BR (1) BRPI0615101A2 (es)
CA (1) CA2620466A1 (es)
EC (1) ECSP088288A (es)
IL (1) IL189434A0 (es)
NO (1) NO20081479L (es)
RU (1) RU2406723C9 (es)
TW (1) TW200738659A (es)
UY (1) UY29767A1 (es)
WO (1) WO2007027134A1 (es)

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TW200745067A (en) * 2006-03-14 2007-12-16 Astrazeneca Ab Novel compounds
JP5040261B2 (ja) * 2006-09-28 2012-10-03 東洋紡績株式会社 (置換プロピルスルファニル)−アルキルアルコールの製造方法
TW200825084A (en) 2006-11-14 2008-06-16 Astrazeneca Ab New compounds 521
TW200833670A (en) 2006-12-20 2008-08-16 Astrazeneca Ab Novel compounds 569
GB0702458D0 (en) * 2007-02-08 2007-03-21 Astrazeneca Ab Salts 668
GB0703999D0 (en) * 2007-03-01 2007-04-11 Astrazeneca Ab New combination 667
GB0704000D0 (en) * 2007-03-01 2007-04-11 Astrazeneca Ab Salts 670
WO2009037503A2 (en) * 2007-09-18 2009-03-26 Astrazeneca Ab New combination - 012 for the treatment of respiratory diseases
PT2242759E (pt) 2008-02-06 2012-12-17 Astrazeneca Ab Compostos
KR20110010725A (ko) * 2008-05-13 2011-02-07 아스트라제네카 아베 무스카린성 수용체 길항제 및 β2­아드레날린수용체 효능제를 포함하는 제약 생성물
MX2010012189A (es) 2008-05-13 2011-03-02 Astrazeneca Ab Derivados de quinuclidina como antagonistas del receptor m3 muscarinico.
WO2009142568A1 (en) * 2008-05-20 2009-11-26 Astrazeneca Ab Combination of (a) glucocorticoid receptor modulator and (b) a b2-agonist
EA201001747A1 (ru) 2008-06-18 2011-08-30 Астразенека Аб Бензоксазиноновые производные, действующие в качестве агониста бета-2-адренорецептора, для лечения респираторных расстройств
JP2011524897A (ja) * 2008-06-20 2011-09-08 アストラゼネカ・アクチエボラーグ β2−アドレナリン受容体活性の調節のための、4−ヒドロキシ−2−オキソ−2,3−ジヒドロ−1,3−ベンゾチアゾール−7−イル化合物を含む医薬組成物
GB0814728D0 (en) * 2008-08-12 2008-09-17 Argenta Discovery Ltd New combination
GB0913345D0 (en) 2009-07-31 2009-09-16 Astrazeneca Ab New combination 802
GB0913342D0 (en) 2009-07-31 2009-09-16 Astrazeneca Ab Compounds - 801
GB201107985D0 (en) * 2011-05-13 2011-06-29 Astrazeneca Ab Process
JO3192B1 (ar) 2011-09-06 2018-03-08 Novartis Ag مركب بنزوثيازولون

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TW200738659A (en) 2007-10-16
IL189434A0 (en) 2008-06-05
KR20080038373A (ko) 2008-05-06
EP1937656A1 (en) 2008-07-02
AU2006285448A1 (en) 2007-03-08
CA2620466A1 (en) 2007-03-08
UY29767A1 (es) 2007-03-30
RU2008110917A (ru) 2009-10-10
JP2009507788A (ja) 2009-02-26
US20090221653A1 (en) 2009-09-03
WO2007027134A1 (en) 2007-03-08
ECSP088288A (es) 2008-04-28
BRPI0615101A2 (pt) 2011-05-03
RU2406723C2 (ru) 2010-12-20
EP1937656A4 (en) 2010-05-05

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