5-bromopyridin-3-ol

N#CCOc1cncc(Br)c1
Reaction #179423
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)NC(COc1cncc(Br)c1)C(C)(C)O[SiH2]C(C)(C)C
Reaction #200217
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Brc1cncc(OCc2ccccc2)c1
Reaction #225723
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=S(=O)(c1ccc(Oc2cncc(Br)c2)cc1)N1CCCC1
Reaction #230790
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)N1CCCC1COc1cncc(Br)c1
Reaction #249751
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=[N+]([O-])c1ccc(N=Nc2ncc(O)cc2Br)cc1
Reaction #269927
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
FC(F)Oc1cncc(Br)c1
Reaction #285815
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CS(=O)(=O)Oc1cncc(Br)c1
Reaction #291455
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Brc1cncc(OCc2ccccc2)c1
Reaction #331765
title compound
المردود 31.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
—
Reaction #356316
solid
المردود 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
Oc1cc(Br)cnc1Cl
Reaction #369424
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=S(=O)(Oc1cncc(Br)c1)N1CCOCC1
Reaction #376145
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1ccc(F)c(-c2ccc(COc3cncc(Br)c3)cc2C(C)(C)C)c1
Reaction #377410
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Brc1cncc(OCc2ccccc2)c1
Reaction #427402
3-(benzyloxy)-5-bromopyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(C)(C)OC(=O)N1CCC[C@H]1COc1cncc(Br)c1
Reaction #452984
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CC(C)(C)OC(=O)N1CC[C@H]1COc1cncc(Br)c1
Reaction #453012
title compound
المردود 47.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
O=[N+]([O-])c1ccc(N=Nc2ncc(O)cc2Br)cc1
Reaction #453041
title compound
المردود 33.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CC(C)(C)OC(=O)N1CC[C@H]1COc1cncc(Br)c1
Reaction #454239
5-bromo-3-((1-t-butyloxycarbonyl-(2S)-azetidinyl)methoxy)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
O=[N+]([O-])c1ccc(N=Nc2ncc(O)cc2Br)cc1
Reaction #454250
title compound
المردود 33735.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CC(C)Oc1cncc(Br)c1
Reaction #532787
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
الصفحة 1التالي