An 59 Reaktionen beteiligt

1147607

COc1ncc(-c2cccc(F)n2)c(OC)n1
Reaction #40981
title compound
Ausbeute 57.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)Nc1c(-c2ccc(C#Cc3cccc(F)n3)s2)nc2cnccn12
Reaction #57391
N-tert-butyl-2-(5-((6-fluoropyridin-2-yl)ethynyl)thiophen-2-yl)imidazo[1,2-a]pyrazin-3-amine
Ausbeute 30.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
FC1(F)CC1COc1cccc(Br)n1
Reaction #68789
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Fc1cccc(-n2ncc3cnc(Cl)cc32)n1
Reaction #86084
6-Chloro-1-(6-fluoro-2-pyridyl)pyrazolo[4,3-c]pyridine
Ausbeute 55.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)OC(=O)N1CCCN(c2cccc(Br)n2)CC1
Reaction #86121
tert-butyl 4-(6-bromopyridin-2-yl)-1,4-diazepane-1-carboxylate
Ausbeute 50.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)OC(=O)N1CCCN(c2cccc(Br)n2)CC1
Reaction #86141
tert-butyl 4-(6-bromopyridin-2-yl)-1,4-diazepane-1-carboxylate
Ausbeute 50.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC1CCC(NC(=O)OC(C)(C)C)CN1c1cccc(Br)n1
Reaction #86155
tert-butyl N-[1-(6-bromo-2-pyridyl)-6-methyl-3-piperidyl]carbamate
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
OC1CNCCN(c2cccc(Br)n2)C1
Reaction #86175
1-(6-bromopyridin-2-yl)-1,4-diazepan-6-ol
Ausbeute 54.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(Br)nc1F
Reaction #86184
6-bromo-2-fluoro-3-methyl-pyridine
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
OCc1ccc(Br)nc1F
Reaction #86195
(6-bromo-2-fluoro-3-pyridyl)methanol
Ausbeute 36.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cn1cc(-c2cc3c(cn2)cnn3-c2cccc(N3CCNC[C@@H](O)C3)n2)cn1
Reaction #86221
solid
Ausbeute 24.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cn1cc(-c2cc3c(cn2)cnn3-c2cccc(N3CCNC[C@H](O)C3)n2)cn1
Reaction #86223
solid
Ausbeute 23.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
OC1CNCCN(c2cccc(Br)n2)C1
Reaction #86242
1-(6-Bromopyridin-2-yl)-1,4-diazepan-6-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cn1cc(-c2cc3c(cn2)cnn3-c2cccc(N3CC4(CNC4)C3)n2)cn1
Reaction #86269
solid
Ausbeute 26.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)Nc1c(-c2ccc(C#Cc3cccc(F)n3)s2)nc2cnccn12
Reaction #186598
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCOc1ccc2cc(-c3cccc(F)n3)ccc2c1
Reaction #207298
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(CNc2cccc(Br)n2)CCOCC1
Reaction #234771
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1(C)OB(c2cccc(F)n2)OC1(C)C
Reaction #308323
6-fluoro-2-pyridylboronic acid pinacol ester
Ausbeute 67.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
C=Cc1cccc(F)n1
Reaction #317967
compound
Ausbeute 35.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Fc1cccc(COc2cccc(Br)n2)c1
Reaction #374340
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
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