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13797

CCOC(=O)c1cnc(N2CCc3ccccc32)nc1O
Reaction #7510
title compound
Ausbeute 77.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N2CCc3ccccc32)nc1OCc1ccc(F)cc1
Reaction #7511
title compound
Ausbeute 79.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N2CCc3ccccc32)nc1OCc1ccc(OC)cc1
Reaction #7512
title compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N2CCc3ccccc32)nc1Cl
Reaction #7513
title compound
Ausbeute 477.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N2CCc3ccccc32)nc1OCc1ccc(OC(F)(F)F)cc1
Reaction #7514
title compound
Ausbeute 53.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N2c3ccccc3C[C@H]2C)nc1OC(C)c1ccccc1
Reaction #7528
ethyl 2-[(R)-2-methyl-2,3-dihydro-1H-indol-1-yl]-4-[(RS)-1-phenylethoxy]-5-pyrimidinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cnc(N2CCc3ccccc32)nc1OCc1ccc(F)cc1
Reaction #7529
2-(2,3-dihydro-1H-indol-1-yl)-4-[(4-fluorobenzyl)oxy]-5-pyrimidinecarboxylic acid
Ausbeute 101.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COc2nc(N3CCc4ccccc43)ncc2C(=O)O)cc1
Reaction #7531
2-(2,3-dihydro-1H-indol-1-yl)-4-[(4-methoxybenzyl)oxy]-5-pyrimidinecarboxylic acid
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N2CCc3ccccc32)nc1OCc1ccc(OC)cc1
Reaction #285848
DOI: 10.1039/C8SC04228D
O=C(O)c1cnc(N2CCc3ccccc32)nc1OCc1ccc(F)cc1
Reaction #393788
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cnc(N2CCc3ccccc32)nc1OCc1ccc(F)cc1
Reaction #1025085
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cnc(N2CCc3ccccc32)nc1O
Reaction #1201006
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cnc(N2CCc3ccccc32)nc1OCc1ccc(OC(F)(F)F)cc1
Reaction #1211691
DOI: 10.1039/C8SC04228D
COc1ccc(COc2nc(N3CCc4ccccc43)ncc2C(=O)O)cc1
Reaction #1309174
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cnc(N2CCc3ccccc32)nc1Cl
Reaction #1632682
DOI: 10.1039/C8SC04228D