4-bromo-2-methoxypyridine

COc1cc(N2CC(NC(=O)OC(C)(C)C)C2)ccn1
Reaction #232
Ausbeute 100.3%750 AstraZeneca ELN dataset
COc1cc(N2CC(NC(=O)OC(C)(C)C)C2)ccn1
Reaction #233
Ausbeute 100.0%750 AstraZeneca ELN dataset
COC(=O)[C@H](Cc1ccnc(OC)c1)NC(=O)OC(C)(C)C
Reaction #87075
(S)-methyl 2-(tert-butoxycarbonylamino)-3-(2-methoxypyridin-4-yl)propanoate
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1cc(OCc2ccc(C(F)(F)F)nc2)ccn1
Reaction #243714
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc(-c2ccc(C[C@H](NC(=O)C3(NC(=O)OC(C)(C)C)CCOCC3)C(N)=O)cc2)ccn1
Reaction #304145
sub-titled compound
Ausbeute 88.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COc1cc(C#Cc2ccc([C@H](C)N3CC[C@](CC(C)(C)O)(c4ccccc4)OC3=O)cc2)ccn1
Reaction #421089
(S)-6-(2-hydroxy-2-methylpropyl)-3-((S)-1-(4-((2-methoxypyridin-4-yl)ethynyl)phenyl)ethyl)-6-phenyl-1,3-oxazinan-2-one
Ausbeute 10.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
COc1cc(OCc2ccc(C(F)(F)F)nc2)ccn1
Reaction #556868
title compound
Ausbeute 72.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
COc1cc(N2CCN(c3cnccc3C3CC3)C2=O)ccn1
Reaction #610718
product
Ausbeute 52.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
COc1cc(N2C(=O)N(C(=O)OCc3ccccc3)C3CC32)ccn1
Reaction #610763
product
Ausbeute 41.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CCOC(=O)Cc1ccnc(OC)c1
Reaction #613577
ethyl 2-(2-methoxypyridin-4-yl)acetate
Ausbeute 38.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
COc1cc(N2CCN(c3cnccc3C3CC3)C2=O)ccn1
Reaction #659562
product
Ausbeute 52.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
COc1cc(N2C(=O)N(C(=O)OCc3ccccc3)C3CC32)ccn1
Reaction #659605
product
Ausbeute 41.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CCOC(=O)Cc1ccnc(OC)c1
Reaction #666077
ethyl 2-(2-methoxypyridin-4-yl)acetate
Ausbeute 38.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
COc1cc(OCc2ccc(C(F)(F)F)nc2)ccn1
Reaction #969214
title compound
Ausbeute 72.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
COc1cc(/C=C/c2ccccc2)ccn1
Reaction #1017820
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
COc1cc(-c2ccc(C)nc2)ccn1
Reaction #1017912
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CSc1ccc(-c2cc[nH]c(=O)c2)cc1
Reaction #1017940
white powder
Ausbeute 77.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
COc1ccc(-c2ccnc(OC)c2)c(F)c1
Reaction #1017956
title compound
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
COc1cc(/C=C/c2ccccc2)ccn1
Reaction #1107735
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
COc1cc(-c2ccc(C)nc2)ccn1
Reaction #1107829
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
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