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CC(C)(C)CN1Cc2c(cc(Cl)c3[nH]ncc23)C[C@@H](CC(=O)N2CCC(c3nc4ccccc4[nH]c3=O)CC2)C1=O
Reaction #219447
Title compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CN1Cc2c(cc(Cl)c3[nH]ncc23)C[C@@H](CC(=O)N2CCC(c3nc4ccccc4[nH]c3=O)CC2)C1=O
Reaction #219662
Title compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2nc(C3CCNCC3)cnc2c1
Reaction #300044
DOI: 10.1039/C8SC04228D
CC(C)(C)CN1Cc2c(cc(Cl)c3[nH]ncc23)CC(CC(=O)N2CCC(c3nc4ccccc4[nH]c3=O)CC2)C1=O
Reaction #1041924
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(c2cnc3ccccc3n2)CC1
Reaction #1153258
1-tert-butoxycarbonyl-4-(quinoxalin-2-yl)piperidine
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2nc(C3CCNCC3)cnc2c1
Reaction #1153259
title compound
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(c2cnc3ccccc3n2)CC1
Reaction #1324260
DOI: 10.1039/C8SC04228D
c1ccc2nc(C3CCN(CCCCn4nnc5ccccc54)CC3)cnc2c1
Reaction #1569824
compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2nc(C3CCN(CCCCn4nnc5ccccc54)CC3)cnc2c1
Reaction #1569842
compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2cn3ccnc3nc2-c2ccc(CN3CCC(c4cnc5ccccc5n4)CC3)cc2)cc1
Reaction #1938444
desired compound
Ausbeute 33.2%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2cn3ccnc3nc2-c2ccc(CN3CCC(c4cnc5ccccc5n4)CC3)cc2)cc1
Reaction #1938464
2-(1-{4-[6-(4-fluorophenyl)-imidazo[1,2-a]pyrimidin-7-yl]-benzyl}-piperidine-4-yl)-quinoxaline
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2cn3ccnc3nc2-c2ccc(CN3CCC(c4cnc5ccccc5n4)CC3)cc2)cc1
Reaction #1938466
2-{1-[4-(6-phenyl-imidazo[1,2-a]pyrimidin-7-yl)-benzyl]-piperidine-4-yl}-quinoxaline
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn2cc(-c3ccccc3)c(-c3ccc(CN4CCC(c5cnc6ccccc6n5)CC4)cc3)nc2n1
Reaction #1938467
2-{1-[4-(2-methyl-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl)benzyl]-piperidine-4-yl}-quinoxaline
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2cn3nc(C4CC4)nc3nc2-c2ccc(CN3CCC(c4cnc5ccccc5n4)CC3)cc2)cc1
Reaction #1938470
pure product
Ausbeute 49.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CN1Cc2c(cc(Cl)c3[nH]ncc23)C[C@@H](CC(=O)N2CCC(c3nc4ccccc4[nH]c3=O)CC2)C1=O
Reaction #2072734
Title compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCC(c2nc3ccccc3nc2OC2CN(c3ccc4ccccc4n3)C2)CC1
Reaction #2295035
benzyl 4-(3-((1-(quinolin-2-yl)azetidin-3-yl)oxy)quinoxalin-2-yl)piperidine-1-carboxylate
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1