5-bromo-2-ethoxy-pyridine

CCOc1ccc(C2(O)CCC3(CC2)OCCO3)cn1
Reaction #190311
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOc1ccc(Br)c(OC)n1
Reaction #417945
3-Bromo-6-ethoxy-2-methoxy-pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CCOC(=O)Cc1ccc(OC)c(-c2ccc(-c3ccc(OCC)nc3)cc2CN(CC)C(=O)OC(C)(C)C)c1
Reaction #650750
[2′-[(tert-Butoxycarbonyl-ethyl-amino)-methyl]-4′-(6-ethoxy-pyridin-3-yl)-6-methoxy-biphenyl-3-yl]-acetic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
CCOC(=O)Cc1ccc(OC)c(-c2ccc(-c3ccc(OCC)nc3)cc2CN(CC)C(=O)OC(C)(C)C)c1
Reaction #785684
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCCc1ccc(C#Cc2ccc(OCC)nc2)cc1
Reaction #919304
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCOc1ccc([SiH](C)C)cn1
Reaction #954579
2-ethoxy-5-dimethylsilylpyridine
收率 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_10
CCOc1ccc(-n2c(C)c(Sc3cccc(C(=O)OC)c3)c3ccc(Cl)cc32)cn1
Reaction #1553991
3-[6-Chloro-1-(6-ethoxy-pyridin-3-yl)-2-methyl-1H-indol-3-ylsulfanyl]-benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_04
CCCC1CCC(C2CCC(c3ccc(OCC)nc3)CC2)CC1
Reaction #1626181
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
C#Cc1ccc(OCC)nc1
Reaction #1650412
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
CCCc1ccc(C#Cc2ccc(OCC)nc2)cc1
Reaction #1677982
1-(4-propylphenyl)-2-(2-ethoxy-pyridine-5-yl)-acetylene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_04
CCC[C@H]1CC[C@H]([C@H]2CC[C@H](c3ccc(OCC)nc3)CC2)CC1
Reaction #1677983
2-ethoxy-5-[trans-4-(trans-4-propylcyclohexyl)cyclohexyl]-pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_04
CCOc1ccc(C2=CCN(C(=O)OC(C)(C)C)CC2)cn1
Reaction #1704500
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
CCOC(=O)C(C)(C)Cc1c(SC(C)(C)C)c2cc(O)ccc2n1Cc1ccc(-c2ccc(OCC)nc2)cc1
Reaction #1707990
desired product
收率 80.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
CCOC(=O)Cc1ccc(OC)c(-c2ccc(-c3ccc(OCC)nc3)cc2CN(CC)C(=O)OC(C)(C)C)c1
Reaction #1712848
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
CCOC(=O)Cc1ccc(OC)c(-c2ccc(-c3ccc(OCC)nc3)cc2CN(CC)C(=O)OC(C)(C)C)c1
Reaction #1897509
[2′-[(tert-Butoxycarbonyl-ethyl-amino)-methyl]-4′-(6-ethoxy-pyridin-3-yl)-6-methoxy-biphenyl-3-yl]-acetic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
C#Cc1ccc(OCC)nc1
Reaction #1975920
title compound
收率 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
CCOc1ccc(N2CCC(=CC#Cc3cccc(C)n3)CC2)cn1
Reaction #1983208
title compound
收率 10.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
CCOc1ccc(C2(O)CCC3(CC2)OCCO3)cn1
Reaction #2183328
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_05
CCOc1ccc([SiH](C)C)cn1
Reaction #2228695
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)