(4-Mercaptophenyl)methanol

Cc1nc(N)nc(O)c1Sc1ccc(CO)cc1
Reaction #242101
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OCc1ccc(SCCl)cc1
Reaction #334246
4-(Chloromethylthio) benzyl alcohol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_11
O=C1OCCC1Sc1ccc(CO)cc1
Reaction #374524
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
N#Cc1ccc(Sc2ccc(CO)cc2)cn1
Reaction #768191
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
N#Cc1cncc(Sc2ccc(CO)cc2)c1
Reaction #908149
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=C(c1nnc(-c2ccccc2)o1)N1CC(Sc2ccc(CO)cc2)C1
Reaction #1122410
60A
収率 61.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
O=C(c1nnc(-c2ccccc2)o1)N1CC(Sc2ccc(CO)cc2)C1
Reaction #1648222
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
Cc1nc(N)nc(O)c1Sc1ccc(CO)cc1
Reaction #1704435
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
O=C(c1nnc(-c2ccccc2)o1)N1CC(Sc2ccc(CO)cc2)C1
Reaction #1726691
5A
収率 61.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_02
O=C1OCCC1Sc1ccc(CO)cc1
Reaction #2075010
product
収率 73.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_06
N#Cc1cncc(Sc2ccc(CO)cc2)c1
Reaction #2354233
title compound
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
N#Cc1ccc(Sc2ccc(CO)cc2)cn1
Reaction #2354235
title compound
収率 28.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12
OCc1ccc(SCCl)cc1
Reaction #2397351
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)
Cc1nc(N)nc(O)c1Sc1ccc(CO)cc1
Reaction #2475087
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_09