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1234433

O=c1[nH]cnc2nc(F)ccc12
Reaction #79113
7-fluoropyrido[2,3-d]pyrimid-4(3H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)CCc2ccc(NC(=O)c3ccc(F)nc3NC3CCCCC3)cc21
Reaction #377507
DOI: 10.1039/C8SC04228D
CN1C(=O)CCc2ccc(NC(=O)c3ccc(F)nc3NC3CCCCC3)cc21
Reaction #513170
2-(cyclohexylamino)-6-fluoro-N-(1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-7-yl)nicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)CCc2ccc(NC(=O)c3ccc(N4CCCCC4)nc3NC3CCCCC3)cc21
Reaction #513200
2-(cyclohexylamino)-N-(1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-7-yl)-6-piperidin-1-ylnicotinamide
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]cnc2nc(F)ccc12
Reaction #1146811
7-fluoropyrido[2,3-d]pyrimid-4(3H)-one
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]cnc2nc(F)ccc12
Reaction #1369157
7-fluoropyrido[2,3-d]pyrimid-4(3H)-one
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]cnc2nc(F)ccc12
Reaction #1473392
7-fluoropyrido[2,3-d]pyrimid-4(3H)-one
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(NC(=O)c2ccc(F)nc2NCc2ccncc2)cc1
Reaction #1902382
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)CCc2ccc(NC(=O)c3ccc(N4CCCCC4)nc3NC3CCCCC3)cc21
Reaction #2211398
DOI: 10.1039/C8SC04228D
O=c1[nH]cnc2nc(F)ccc12
Reaction #2343357
7-fluoropyrido[2,3-d]pyrimid-4(3H)-one
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]cnc2nc(F)ccc12
Reaction #2374926
7-fluoropyrido[2,3-d]pyrimid-4(3H)-one
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1