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Preparation of 5-HT receptor modulators
专利权人:
ABBVIE INC.;ABBVIE DEUTSCHLAND GMBH & CO KG
发明人:
WELCH, DENNIE S.,AKRITOPOULOU-ZANZE, IRINI,BRAJE, WILFRIED,DJURIC, STEVAN W.,WILSON, NOEL S.,TURNER, SEAN C.,KRUGER, ALBERT W.,RELO, ANA-LUCIA,SHEKAR, SHASHANK,ZHAO, HONGYU,GANDARILLA, JORGE,GASIECKI,
申请号:
ES13161013
公开号:
ES2535490T3
申请日:
2010.05.20
申请国别(地区):
ES
年份:
2015
代理人:
摘要:
A process for preparing a compound of formula (1-5): ** Formula ** or a pharmaceutically acceptable salt thereof, where A is selected from the group consisting of ** Formula ** X1 is N or CR9; X2 is N or CR10; X3 is N or CR11; X4 is N or CR12; with the proviso that only one or two of X1, X2, X3, or X4 can be N; R9, R10, R11, R12, R13, R14, R15 and R16 each is independently hydrogen, alkyl, alkenyl, alkynyl, halogen, cyano, -G1, -G2, -NO2, -OR1a, -OC (O) R1a, -OC (O) N (Rb) (R3a), -SR1a, -S (O) R2a, -S (O) 2R2a, - S (O) 2N (Rb) (R3a), -C (O) R1a, -C (O) G3, -C (O) OR1a, -C (O) N (Rb) (R3a), -N (Rb) (R3a), -N (RaC (O) R1a, -N (Ra) C (O) O (R1a), - N (Ra) C (O) N (Rb) (R3a), -N (Ra) S (O) 2 (R2a), - (CR4aR5a) m-NO2- (CR4aR5a ) m-OR1a, - (CR4aR5a) m-OC (O) R1a, - (CR4aR5a) m- OC (O) N (Rb) (R3a), - (CR4aR5a) m-SR1a, - (CR4aR5a) mS (O ) R2a, - (CR4aR5a) mS (O) 2R2a, - (CR4R5a) S (O) 2N (Rb) (R3a), - (CR4aR5a) m (O) R1a, - (CR4aR5a) mC (O) OR1a, - (CR4aR5a) mC (O) N (Rb) (R3a), - (CR4aR5a) mN (Rb) (R3a), - (CR4aR5a) m- N (Ra) C (O) R1a, - (CR4aR5a) mN (Ra ) C (O) O (R1a), - (CR4aR5a) mN (Ra) C (O) N (Rb) (R3a), - (CR4aR5a) m-G1, -CR4a>; = CR5a-G1, - (CR4aR5a) m-G2, -CR4a>; = CR5a-G2, -CR6a-C (R7a) 2, cyanoalkyl, haloalkyl, (v), (vi), (vii) or (viii); where ** Formula ** R1a and R3a , in each case, each is independently hydrogen, alkyl, haloalkyl G1, - (CR4aR5a) m-G1, G2, or - (CR4aR5a) m-G2; R2a, in each case, is independently alkyl, haloalkyl, G1, or - (CR4aR5a) m-G1; R6a is alkyl or haloalkyl; R7a in each case, is independently hydrogen, alkyl, or haloalkyl; R4a and R5a, in each case, each is independently hydrogen, halogen, alkyl, or haloalkyl; G1, in each case, is independently aryl or heteroaryl, where each G1 is independently unsubstituted or substituted with 1, 2, 3, 4 or 5 substituents selected from the group consisting of alkyl, alkenyl, alkynyl, halogen, cyano, - NO2, -OR1b, -OC (O) R1b, -OC (O) N (Rb) (R3b), -SR1b, -S (O) R2b, -S (O) 2R2b, - S (O) 2N (Rb )
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