2,3-dichloropyridine

O=C(Nc1ncccc1Cl)c1ccccc1
Reaction #719
수율 10.8%750 AstraZeneca ELN dataset
Clc1cccnc1N1CCc2ncnc(Nc3ccccc3)c2C1
Reaction #47902
desired compound
수율 25.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1ccc(Nc2ncnc3c2CN(c2ncccc2Cl)CC3)cc1
Reaction #47905
desired compound
수율 30.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
FC(F)(F)c1ccc(Nc2ncnc3c2CN(c2ncccc2Cl)CC3)cn1
Reaction #47908
desired compound
수율 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=S(=O)(c1ccc(Nc2ncnc3c2CN(c2ncccc2Cl)CC3)cc1)C(F)(F)F
Reaction #47912
desired compound
수율 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)c1ccc(Nc2ncnc3c2CN(c2ncccc2Cl)CC3)cn1
Reaction #47928
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
FC(F)(F)c1ccc(Nc2ncnc3c2CN(c2ncccc2Cl)CC3)cc1
Reaction #47935
desired compound
수율 26.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Clc1cccnc1-n1ccc(Br)n1
Reaction #74263
2-(3-bromo-1H-pyrazol-1-yl)-3-chloropyridine
수율 68.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
FC(F)(F)c1ccn(-c2ncccc2Cl)n1
Reaction #90213
desired intermediate
수율 75.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Clc1ccn(-c2ncccc2Cl)n1
Reaction #90217
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Clc1cccnc1-n1ccc(Br)n1
Reaction #90222
pink solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)Oc1ncccc1Cl
Reaction #179088
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CCN(c2ncccc2Cl)CC1
Reaction #184885
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=S(=O)(c1ccc(Cl)cc1)C1CCN(c2ncccc2Cl)CC1
Reaction #193926
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CN(c2ncccc2Cl)CC(C)N1S(=O)(=O)c1ccc(C(C)(C)C)cc1
Reaction #210766
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
FC(F)(F)c1ccn(-c2ncccc2Cl)n1
Reaction #223216
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(-c2ncccc2Cl)cc1
Reaction #225863
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Clc1cccnc1-n1ccc(Br)n1
Reaction #227190
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc(-c2ncccc2Cl)ccc1Cl
Reaction #230894
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C(C(=O)OCC)c1ncccc1Cl
Reaction #240659
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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