发明名称 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors
摘要 The present invention provides derivatives of pyrido[2,3-d]pyrimidin-7-one. These compounds are kinase inhibitors, including compounds that show anti-proliferative activity, including against tumor cells, and are useful in the treatment of diseases including cancer.
申请公布号 US2014163007(A1) 申请公布日期 2014.06.12
申请号 US201313949743 申请日期 2013.07.24
申请人 Forma Therapeutics, Inc. 发明人 MURTHI KRISHNA;CASAUBON REBECCA;KLUGE ARTHUR F.;SMITH CHASE;VOGT JOACHIM
分类号 C07D471/04 主分类号 C07D471/04
代理机构 代理人
主权项 1. A compound having a structure represented by formula (V) or any tautomeric or stereoisomeric form thereof, wherein R7 is selected from —S(O)m—R17, with m=0, 1 or 2, and —N(R1)—V—R2; R18 is taken from the list of —W—R4, —COOH, —COOR17, and —Br; and R17 is independently selected from —C1-6-alkyl, —CH2-aryl, or -aryl; with R1 is selected from hydrogen, —C1-6alkyl, —C2-6-alkenyl, —C2-6-alkynyl, —C3-6-cycloalkyl and —C3-6-cycloalkenyl; V is selected from a bond, —O—, —N(R11)—, —C(═X)—, —S(O)n—, —C(═X)—O—, —C(═X)—N(R11)—, —C(═X)—S—, —C(═X)—N(R11)—N(R11)—, —N(R11)—C(═X)—, —N(R11)—C(═X)—N(R11)—, and —N(R11)—S(O)n—, with n=1 or 2; R2 is selected from hydrogen, -alkyl, -alkenyl, -alkynyl, -cycloalkyl, -cycloalkenyl, -heterocycloalkyl, -heterocycloalkenyl, -aryl and -heteroaryl; or, R1 and R2, together with V and the nitrogen atom they are attached to, form a heterocycle; R3 is selected from hydrogen, —C1-6alkyl, —C2-6-alkenyl, —C2-6-alkynyl, —C3-6-cycloalkyl, —C3-6-cycloalkenyl and halogen; W is a bond, or —C(═O)—; R4 is selected from hydrogen, phenyl ans substituted phenyl; R5 is selected from -alkyl, -alkenyl, -alkynyl, -cycloalkyl, -cycloalkenyl, —(C-linked-heterocycloalkyl), —(C-linked-heterocycloalkenyl), -aryl, and -heteroaryl; X is independently selected from ═O, ═S, ═NR12, ═N—OR13, ═N—N(R11)2, ═N—N(R11)(R12), and ═N—N(R12)2; R10 is independently selected from —C1-6alkyl, —C2-6-alkenyl, —C2-6-alkynyl, —C3-6-cycloalkyl and —C3-6-cycloalkenyl; R11 is independently selected from hydrogen and R10; R12 is independently selected from -alkyl, -alkenyl, -alkynyl, -cycloalkyl, -cycloalkenyl, -heterocycloalkyl, -heterocycloalkenyl, -aryl and -heteroaryl; R13 is independently selected from hydrogen and R12; wherein R2, R4, R5, R10, and R12 may optionally be substituted; provided that if R7 is —N(R1)—V—R2, then R18 is not —W—R4.
地址 Watertown MA US