发明名称 NOVEL AZABENZIMIDAZOLE HEXAHYDROFURO[E,2-B]FURAN DERIVATIVES
摘要 Novel compounds of the structural formula (I) are activators of AMP-protein kinase and may be useful in the treatment, prevention and suppression of diseases mediated by the AMPK activated protein kinase. The compounds of the present invention may be useful in the treatment of Type 2 diabetes, hyperglycemia, metabolic syndrome, obesity, hypercholesterolemia, and hypertension.;
申请公布号 US2015284411(A1) 申请公布日期 2015.10.08
申请号 US201314419774 申请日期 2013.08.19
申请人 APGAR James M.;ARASAPPAN Ashok;BIFTU Tesfaye;CHEN Ping;FENG Danqing;GUIDRY Erin;HICKS Jacqueline;KEKEC Ahmet;LEAVITT Kenneth;LI Bing;MCCRACKEN Troy;SEBHAT Iyassu;QIAN Xiaoxia;WEI Lan;WILKENING Robert;WU Zhicai;Merck Sharp & Dohme Corp. 发明人 Apgar James M.;Arasappan Ashok;Biftu Tesfaye;Chen Ping;Feng Danqing;Guidry Erin;Hicks Jacqueline D.;Kekec Ahmet;Leavitt Kenneth J.;Li Bing;McCracken Troy;Sebhat Iyassu;Qian Xiaoxia;Wei Lan;Wilkening Robert R.;Wu Zhicai
分类号 C07D519/00;A61K31/438;A61K45/06;A61K31/501;A61K31/5377;A61K31/541;A61K31/437;A61K31/506 主分类号 C07D519/00
代理机构 代理人
主权项 1. A compound of structural formula I: or a pharmaceutically acceptable salt thereof, wherein: T is selected from the group consisting of: CR3, N and N-oxide; U is selected from the group consisting of: CR1, N and N-oxide; V is selected from the group consisting of: CR2, N and N-oxide; W is selected from the group consisting of: CR4, N and N-oxide, provided that at least one of T, U, V and W is N or N-oxide; X is selected from: (1) —CH2—,(2) —CHF—,(3) —CF2—,(4) —S—,(5) —O—,(6) —O—CH2—,(7) —O—CH2CH2—,(8) —NH—,(9) —C(O)—,(10) —NHC(O)—,(11) —C(O)NH—,(12) —NHSO2—,(13) —SO2NH—, and(14) —CO2—, wherein each CH2 is unsubstituted or substituted with 1 or 2 substituents selected from: hydroxy, halogen, NH2, C1-6alkyl, CO2H, CO2C1-6alkyl, COC1-6alkyl, phenyl and —CH2phenyl, and wherein each NH is unsubstituted or substituted with 1 substituent selected from: C1-6alkyl, CO2H, CO2C1-6alkyl, COC1-6alkyl, phenyl and —CH2phenyl; Y is selected from: wherein A is selected from: CH2, NH, NC1-6alkyl, O and S, and wherein Y is unsubstituted or substituted with 1, 2, 3 or 4 substituents selected from Rb; Z is selected from: (1) NR5,(2) —S—, and(3) —O—; each R1 and R2 is independently selected from: (1) hydrogen,(2) halogen,(3) CN,(4) CF3,(5) —C1-6alkyl,(6) —C2-6alkenyl,(7) —C2-6alkynyl,(8) —(CH2)pC3-10cycloalkyl,(9) —(CH2)pC3-7cycloalkyl-aryl,(10) —(CH2)pC3-7cycloalkyl-heteroaryl,(11) —(CH2)pC4-10cycloalkenyl,(12) —(CH2)pC4-7cycloalkenyl-aryl,(13) —(CH2)pC4-7cycloalkenyl-heteroaryl,(14) —(CH2)pC2-10cycloheteroalkyl,(15) —(CH2)pC2-10cycloheteroalkenyl,(16) —(CH2)paryl,(17) —(CH2)paryl-C1-8alkyl,(18) —(CH2)paryl-C2-8alkenyl,(19) —(CH2)paryl-C2-8alkynyl-C1-8alkyl,(20) —(CH2)paryl-C2-8alkynyl-C3-7cycloalkyl,(21) —(CH2)paryl-C2-8alkynyl-C3-7cycloalkenyl,(22) —(CH2)paryl-C2-8alkynyl-C2-10cycloheteroalkyl,(23) —(CH2)paryl-C2-8alkynyl-C2-10cycloheteroalkenyl,(24) —(CH2)paryl-C2-8alkynyl-aryl,(25) —(CH2)paryl-C2-8alkynyl-heteroaryl,(26) —(CH2)paryl-C3-7cycloalkyl,(27) —(CH2)paryl-C3-7cycloalkenyl,(28) —(CH2)paryl-C2-10cycloheteroalkyl,(29) —(CH2)paryl-C2-10cycloheteroalkenyl,(30) —(CH2)paryl-aryl,(31) —(CH2)paryl-heteroaryl,(32) —(CH2)pheteroaryl,(33) —(CH2)pheteroaryl-C3-7cycloalkyl,(34) —(CH2)pheteroaryl-C2-10cycloheteroalkyl,(35) —(CH2)pheteroaryl-C2-10cycloheteroalkenyl,(36) —(CH2)pheteroaryl-aryl,(37) —(CH2)pheteroaryl-heteroaryl,(38) —C2-6alkenyl-alkyl,(39) —C2-6alkenyl-aryl,(40) —C2-6alkenyl-heteroaryl,(41) —C2-6alkenyl-C3-7cycloalkyl,(42) —C2-6alkenyl-C3-7cycloalkenyl,(43) —C2-6alkenyl-C2-7cycloheteroalkyl,(44) —C2-6alkenyl-C2-7cycloheteroalkenyl,(45) —C26alkynyl-(CH2)1-3—O-aryl,(46) —C2-6alkynyl-alkyl,(47) —C2alkynyl-aryl,(48) —C2alkynyl-heteroaryl,(49) —C2-6alkynyl-C3-7cycloalkyl,(50) —C2-6alkynyl-C3-7cycloalkenyl,(51) —C2-6alkynyl-C2-7cycloheteroalkyl,(52) —C2-6alkynyl-C2-7cycloheteroalkenyl, and(53) —C(O)NH—(CH2)0-3phenyl, wherein each CH2 is unsubstituted or substituted with 1 or 2 substituents selected from: halogen, CF3, —OH, —NH2, —C1-6alkyl, —OC1-6alkyl, —NHC1-6alkyl, and —N(C1-6alkyl)2, wherein each alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, cycloheteroalkyl, cycloheteroalkenyl, phenyl, aryl and heteroaryl is unsubstituted or substituted with 1, 2, 3 or 4 substituents independently selected from Ra, provided that at least one of and only one of R1 and R2 is selected from the group consisting of: hydrogen, halogen, —CN, —CF3, —C1-6alkyl, C2-6alkenyl and C2-6alkynyl; R3 and R4 are each independently absent or selected from: (1) hydrogen,(2) halogen,(3) —C1-6alkyl,(4) —C2-6alkenyl,(5) —C2-6alkynyl,(6) —C3-10cycloalkyl,(7) —C3-10cycloalkenyl,(8) aryl,(9) heteroaryl,(10) —CN,(11) —CF3,(12) —OH,(13) —OC1-6alkyl,(14) —NH2,(15) —NHC1-6alkyl,(16) —N(C1-6alkyl)2,(17) —SC1-6alkyl,(18) —SOC1-6alkyl,(19) —SO2C1-6alkyl,(20) —NHSO2C1-6alkyl,(21) —NHC(O)C1-6alkyl,(22) —SO2NHC1-6alkyl, and(23) —C(O)NHC1-6alkyl; R5 is selected from: (1) hydrogen,(2) —C1-6alkyl,(3) C1-6alkenyl,(4) —(CH2)uOH,(5) —CH2CO2H, and(6) —CH2CO2C1-6alkyl; each Ra is independently selected from the group consisting of: (1) —(CH2)m-halogen,(2) oxo,(3) —(CH2)mOH,(4) —(CH2)mN(Rj)2,(5) —(CH2)mNO2,(6) —(CH2)mCN,(7) —C1-6alkyl,(8) —(CH2)mCF3,(9) —(CH2)mOCF3,(10) —O—(CH2)m—OC1-6alkyl,(11) —(CH2)mN(Rj)C(O)Rf,(12) —(CH2)mN(Rj)CO2Rf,(13) —(CH2)mC(═N—OH)N(Rj)2,(14) —(CH2)mOC1-6alkyl,(15) —(CH2)mO—(CH2)m—C3-7cycloalkyl,(16) —(CH2)mO—(CH2)m—C2-7cycloheteroalkyl,(17) —(CH2)mO—(CH2)m-aryl,(18) —(CH2)mO—(CH2)m-heteroaryl,(19) —(CH2)mSC1-6alkyl,(20) —(CH2)mS(O)C1-6alkyl,(21) —(CH2)mSO2C1-6alkyl,(22) —(CH2)mO—SO2C1-6alkyl,(23) —(CH2)mSO2(CH2)m—C3-7cycloalkyl,(24) —(CH2)mSO2(CH2)m—C2-7cycloheteroalkyl,(25) —(CH2)mSO2(CH2)m-aryl,(26) —(CH2)mSO2(CH2)m-heteroaryl,(27) —(CH2)mSO2NH2,(28) —(CH2)mSO2NHC1-6alkyl,(29) —(CH2)mSO2NHC3-7cycloalkyl,(30) —(CH2)mSO2NHC2-7cycloheteroalkyl,(31) —(CH2)mSO2NH-aryl,(32) —(CH2)mSO2NH-heteroaryl,(33) —(CH2)mNHSO2—C1-6alkyl,(34) —(CH2)mNHSO2—C3-7cycloalkyl,(35) —(CH2)mNHSO2—C2-7cycloheteroalkyl,(36) —(CH2)mNHSO2-aryl,(37) —(CH2)mNHSO2NH-heteroaryl,(38) —(CH2)mN(Rj)—C1-6alkyl,(39) —(CH2)mN(Rj)—C3-7cycloalkyl,(40) —(CH2)mN(Rj)—(CH2)m—C3-7cycloalkyl,(41) —(CH2)mN(Rj)—C2-7cycloheteroalkyl,(42) —(CH2)mN(Rj)—(CH2)m—C2-7cycloheteroalkyl,(43) —(CH2)mN(Rj)—C2-7cycloheteroalkenyl,(44) —(CH2)mN(Rj)—(CH2)m—C2-7cycloheteroalkenyl,(45) —(CH2)mN(Rj)-aryl,(46) —(CH2)mN(Rj)—(CH2)m-aryl,(47) —(CH2)mN(Rj)-heteroaryl,(48) —(CH2)mN(Rj)—(CH2)m-heteroaryl,(49) —(CH2)mC(O)Rf,(50) —(CH2)mC(O)N(Rj)2,(51) —(CH2)mN(Rj)C(O)N(Rj)2,(52) —(CH2)mCO2H,(53) —(CH2)mOCOH,(54) —(CH2)mCO2Rf,(55) —(CH2)mOCORf,(56) —(CH2)mC3-7cycloalkyl,(57) —(CH2)mC3-7cycloalkenyl,(58) —(CH2)mC2-6cycloheteroalkyl,(59) —(CH2)mC2-6cycloheteroalkenyl,(60) —(CH2)maryl, and(61) —(CH2)mheteroaryl, wherein each CH2 is unsubstituted or substituted with 1 or 2 substituents selected from: oxo, —OH, —(CH2)1-3OH, —CN, —NH2, —NH(C1-6alkyl), —N(C1-6alkyl)2, —C1-6alkyl, —C1-6alkyl substituted with 1-5 OH, —OC1-6alkyl, halogen, —CH2F, —CHF2, —CF3, —CO2H, —CO2C1-6alkyl, —C3-7cycloalkyl, phenyl, CH2phenyl, heteroaryl and CH2heteroaryl, and wherein alkyl, cycloalkyl, cycloalkenyl, cycloheteroalkyl, cycloheteroalkenyl, aryl and heteroaryl are unsubstituted or substituted with 1, 2, 3 or 4 substituents selected from: oxo, —OH, —(CH2)1-5OH, —CN, —NH2, —NH(C1-6alkyl), —N(C1-6alkyl)2, —C1-6alkyl, —C1-6alkyl substituted with 1-5 OH, —OC1-6alkyl, halogen, —CH2F, —CHF2, —CF3, —(CH2)1-5CF3 optionally substituted with 1, 2 or 3 —OH, —CO2H, —CO2C1-6alkyl, —SO2C1-6alkyl, —C3-7cycloalkyl, phenyl, CH2phenyl, heteroaryl and CH2heteroaryl; each Rb is independently selected from: (1) hydrogen,(2) —C1-6alkyl,(3) —C1-6alkenyl,(4) —(CH2)nC3-10cycloalkyl,(5) —(CH2)nC3-10cycloalkenyl,(6) —(CH2)nC2-10cycloheteroalkyl,(7) —(CH2)nC2-10cycloheteroalkenyl,(8) —(CH2)naryl,(9) —(CH2)nheteroaryl,(10) oxo,(11) —(CH2)nCF3,(12) —(CH2)nCN,(13) —(CH2)t-halogen,(14) —(CH2)s—OH,(15) —(CH2)nNO2,(16) —(CH2)nNH2,(17) —(CH2)nNH(C1-6alkyl),(18) —(CH2)nN(C1-6alkyl)2,(19) —(CH2)nNHCO2H,(20) —(CH2)nOC1-6alkyl,(21) —(CH2)nOC1-6alkenyl,(22) —(CH2)nCOC1-6alkyl,(23) —(CH2)nCO2H,(24) —(CH2)nOCOH,(25) —(CH2)nCO2Ri,(26) —(CH2)nOC(O)Ri,(27) —(CH2)qC(O)N(Re)2,(28) —(CH2)qCO2N(Re)2,(29) —(CH2)nC(O)(CH2)nN(Rg)2,(30) —(CH2)nOC(O)(CH2)nN(Rg)2,(31) —(CH2)nN(Re)C(O)C1-6alkyl,(32) —(CH2)nN(Re)SO2Ri,(33) —(CH2)nSO2C1-6alkyl,(34) (CH2)nSO2N(Re)Rg,(35) (CH2)nSO2N(Re)C(O)Ri,(36) (CH2)nSO2N(Re)CO2Ri,(37) (CH2)nSO2N(Re)CON(Rg)2,(38) (CH2)nC(O)N(Re)SO2Ri,(39) (CH2)nN(Re)C(O)N(Rg)2,(40) ═N(OH), and(41) ═N(OC1-6alkyl), wherein each CH2 is unsubstituted or substituted with 1 or 2 substituents selected from: —C1-6alkyl, —OH, halogen and —NH2 wherein each NH is unsubstituted or substituted with 1 substituent selected from Rc, and wherein each alkyl, cycloalkyl, cycloalkenyl, cycloheteroalkyl, cycloheteroalkenyl, aryl and heteroaryl is unsubstituted or substituted with 1, 2, 3 or 4 substituents selected from Rc, or wherein two Rb substituents and the carbon to which they are attached may form a 3 to 6 membered cycloalkyl ring, a 3-6 membered cycloalkenyl ring, a 3-6 membered cycloheteroalkyl ring or a 3-6 membered cycloheteroalkenyl ring, wherein the ring is unsubstituted or substituted with 1, 2, 3 or 4 substituents selected from Rc; each Rc is independently selected from: (1) halogen,(2) oxo,(3) —(CH2)rOH,(4) —(CH2)rN(Re)2,(5) —(CH2)rCN,(6) —C1-6alkyl,(7) —CF3,(8) —C1-6alkyl-OH,(9) —OCH2OC1-6alkyl,(10) —(CH2)rOC1-6alkyl,(11) —OCH2aryl,(12) —(CH2)rSC1-6alkyl,(13) (CH2)rC(O)Rf,(14) (CH2)rC(O)N(Re)2,(15) —(CH2)rCO2H,(16) —(CH2)rCO2Rf,(17) —(CH2)rC3-7cycloalkyl,(18) —(CH2)rC2-6cycloheteroalkyl,(19) —(CH2)raryl, and(20) —(CH2)rheteroaryl, wherein each CH2 is unsubstituted or substituted with 1 or 2 substituents selected from: oxo, —OH, —CN, —N(Rh)2, —C1-6alkyl, —OC1-6alkyl, halogen, —CH2F, —CHF2, —CF3, —CO2H, —CO2C1-6alkyl, —C3-7cycloalkyl and heteroaryl, and wherein alkyl, cycloalkyl, cycloheteroalkyl, aryl and heteroaryl are unsubstituted or substituted with 1, 2, 3 or 4 substituents selected from: oxo, —OH, —CN, —N(Rh)2, —C1-6alkyl, —OC1-6alkyl, halogen, —CH2F, —CHF2, —CF3, —CO2H, —CO2C1-6alkyl, —C3-7cycloalkyl and heteroaryl; each Re, Rg and Rh is independently selected from: (1) hydrogen,(2) —C1-6alkyl, and(3) —O—C1-6alkyl, wherein alkyl is unsubstituted or substituted with 1, 2, 3 or 4 substituents selected from: —OH, oxo, halogen, C1-6alkyl, —OC1-6alkyl, —NH2, —NH(C1-6alkyl), and —N(C1-6alkyl)2; each Rj is independently selected from: (1) hydrogen,(2) C1-6alkyl,(3) C3-6cycloalkyl,(4) —C(O)Ri,(5) —CO2Ri, and(6) —SO2Ri, wherein alkyl and cycloalkyl are unsubstituted or substituted with 1, 2, 3 or 4 substituents selected from: —OH, oxo, halogen, C1-6alkyl, —OC1-6alkyl, —NH2, —NH(C1-6alkyl), and —N(C1-6alkyl)2; each Rf and Ri is independently selected from: (1) —C1-6alkyl,(2) —(CH2)rC4-7cycloalkyl,(3) —(CH2)rC4-7cycloalkenyl,(1) —(CH2)rC3-7cycloheteroalkyl,(2) —(CH2)rC3-7cycloheteroalkenyl,(3) —(CH2)raryl, and(4) —(CH2)rheteroaryl, wherein alkyl, cycloalkyl, cycloalkenyl, cycloheteroalkyl, cycloheteroalkenyl, aryl and heteroaryl are unsubstituted or substituted with 1, 2, 3 or 4 substituents selected from: oxo, —OH, —CN, —NH2, —NH(C1-6alkyl), —N(C1-6alkyl)2, —C1-6alkyl, —OC1-6alkyl, halogen, —CH2F, —CHF2, —CF3, —CO2H, —CO2C1-6alkyl, —C3-7cycloalkyl, and heteroaryl; a is 1 or 2; b is 1 or 2; n is 0, 1, 2, 3 or 4; m is 0, 1, 2, 3 or 4; p is 0, 1, 2, or 3; q is 0, 1, 2, 3 or 4; r is 0, 1 or 2; s is 0, 1, 2, 3 or 4; t is 0, 1, 2, 3 or 4, and u is 0,1,2,3 or 4.
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