An 16 Reaktionen beteiligt

Nc1cc(F)ccn1

Nc1cc(F)ccn1
Reaction #256
Ausbeute 25.3%750 AstraZeneca ELN dataset
Cl.Nc1cc(F)c(Br)cn1
Reaction #156329
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)c1cnc2cc(F)ccn12
Reaction #166430
ethyl 7-fluoroimidazo[1,2-a]pyridine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)c1cnc2cc(F)ccn12
Reaction #166602
ethyl 7-fluoroimidazo[1,2-a]pyridine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(Nc1c(F)cccc1F)c1cccc(-c2nc3cc(F)ccn3c2-c2ccnc(Cl)n2)c1
Reaction #506760
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
COc1ccc(-c2nc3cc(F)ccn3c2-c2ccnc(Cl)n2)cc1C(=O)Nc1c(F)cccc1F
Reaction #506764
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
Nc1cc(F)c(Br)cn1
Reaction #683031
5-bromo-4-fluoropyridin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CCOC(=O)c1cnc2cc(F)ccn12
Reaction #793712
ethyl 7-fluoroimidazo[1,2-a]pyridine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CCOC(=O)c1cnc2cc(F)ccn12
Reaction #793799
ethyl 7-fluoroimidazo[1,2-a]pyridine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CCOC(=O)c1cn2ccc(F)cc2n1
Reaction #956796
ethyl 7-fluoroimidazo[1,2-a]pyridine-2-carboxylate
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
CCOC(=O)Cc1cn2ccc(F)cc2n1
Reaction #1008072
product
Ausbeute 17.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CC1(C)OB(c2ccc(C(=O)Nc3cc(F)ccn3)cc2)OC1(C)C
Reaction #1015486
N-(4-fluoropyridin-2-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
Nc1cc(F)c(Br)cn1
Reaction #1038065
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
Nc1cc(F)c(I)cn1
Reaction #1865050
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_02
Nc1cc(O[C@H]2CCOC2)ccn1
Reaction #1865104
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_02
O=C(Nc1cc(F)ccn1)c1cc(Cl)cc(Oc2cncnc2)c1
Reaction #2488682
title compound
Ausbeute 38.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_08