4-Benzyloxy-1-(4-hydroxyphenyl)-1H-pyridin-2-one

CN(C)CCOc1ccc(-n2ccc(OCc3ccccc3)cc2=O)cc1
Reaction #43311
title compound
Ausbeute 66.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(CO)cn1
Reaction #43321
5-hydroxymethyl-2-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)Oc1ccc(/C=C/c2ccn(-c3ccc(OCCN4CCCC4)cc3)c(=O)c2)cc1
Reaction #43331
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCN(CC)CCOc1ccc(-n2ccc(OCc3ccccn3)cc2=O)cc1
Reaction #43338
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=c1nc(OCc2ccc(F)cc2)ccn1-c1ccc(OCCN2CCCC2)cc1
Reaction #43345
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
[N-]=[N+]=NCCOc1ccc(-n2ccc(OCc3ccc(F)cc3)cc2=O)cc1
Reaction #43346
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=c1cc(OCc2ccc(F)cc2)ccn1-c1ccc(OCCN2CCC[C@H]2CF)cc1
Reaction #43349
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=c1cc(OCc2ccc(F)cc2)ccn1-c1ccc(OCCN2CCCC2CF)cc1
Reaction #205137
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(C)CCOc1ccc(-n2ccc(OCc3ccccc3)cc2=O)cc1
Reaction #1638412
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)