3,4,5-trichloropyridine

COc1ccc2c(Nc3c(Cl)cncc3Cl)cc(=O)oc2c1OC1CCCC1
Reaction #48909
8-(cyclopentyloxy)-4-(3,5-dichloropyridin-4-ylamino)-7-methoxy-2H-chromen-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCc1c(Nc2c(Cl)cncc2Cl)c2ccc(OC)c(OCC3CC3)c2oc1=O
Reaction #48911
8-(cyclopropylmethoxy)-4-(3,5-dichloropyridin-4-ylamino)-3-ethyl-7-methoxy-2H-chromen-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc2c(Nc3c(Cl)cncc3Cl)c(F)c(=O)oc2c1OC1CCCC1
Reaction #48921
8-(cyclopentyloxy)-4-(3,5-dichloropyridin-4-ylamino)-3-fluoro-7-methoxy-2H-chromen-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc2c(Nc3c(Cl)cncc3Cl)c(CCOCc3ccccc3)c(=O)oc2c1OC1CCCC1
Reaction #48979
3-(2-(benzyloxy)ethyl)-8-(cyclopentyloxy)-4-(3,5-dichloropyridin-4-ylamino)-7-methoxy-2H-chromen-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=S(=O)(c1ccc(Cl)cc1)C1CCN(c2c(Cl)cncc2Cl)CC1
Reaction #238949
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=S(=O)(c1ccc2ccccc2c1)C1CCN(c2c(Cl)cncc2Cl)CC1
Reaction #283222
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=S(=O)(c1ccc(Cl)c(Cl)c1)C1CCN(c2c(Cl)cncc2Cl)CC1
Reaction #287221
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Nc1ccc(Oc2c(Cl)cncc2Cl)cc1
Reaction #292528
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=Cc1cccn1-c1c(Cl)cncc1Cl
Reaction #339158
1-(3,5-dichloro-4-pyridinyl)-1H-pyrrole-2-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CC(C)(C)c1ccc(S(=O)(=O)C2CCN(c3c(Cl)cncc3Cl)CC2)cc1
Reaction #369623
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1ccc(C(=O)Nc2c(Cl)cncc2Cl)cc1OC1CCCC1
Reaction #444070
N-(3,5-dichloropyrid-4-yl)-3-cyclopentyloxy-4-methoxy-benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
COc1ccc2c(Nc3c(Cl)cncc3Cl)cc(=O)[nH]c2c1OC1CCCC1
Reaction #746240
8-(cyclopentyloxy)-4-(3,5-dichloropyridin-4-ylamino)-7-methoxyquinolin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
COc1ccc2c(Nc3c(Cl)cncc3Cl)cc(=O)[nH]c2c1OCC1CC1
Reaction #766119
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COc1ccc(C(=O)Nc2c(Cl)cncc2Cl)cc1OC1CCCC1
Reaction #784169
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCOC(=O)C1CCN(c2c(Cl)cncc2Cl)CC1
Reaction #1033399
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
COc1ccc2c(Nc3c(Cl)cncc3Cl)cc(=O)[nH]c2c1OC1CCCC1
Reaction #1182949
8-(cyclopentyloxy)-4-(3,5-dichloropyridin-4-ylamino)-7-methoxyquinolin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
COc1ccc2c(Nc3c(Cl)cncc3Cl)cc(=O)[nH]c2c1OCC1CC1
Reaction #1182970
8-(cyclopropylmethoxy)-4-(3,5-dichloropyridin-4-ylamino)-7-methoxy-quinolin-2(1H)-one
Ausbeute 78.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
COc1ccc2c(Nc3c(Cl)cncc3Cl)c(F)c(=O)oc2c1OC1CCCC1
Reaction #1201875
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
[O-][n+]1cc(Cl)c(Cl)c(Cl)c1
Reaction #1279224
title product
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
COc1ccc2c(Nc3c(Cl)cncc3Cl)c(CCOCc3ccccc3)c(=O)oc2c1OC1CCCC1
Reaction #1317110
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
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