مشارك في 21 تفاعل

10406366

Cc1cc(C(=O)OC(C)(C)C)cc(Cl)n1
Reaction #211239
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(C(=O)OC(C)C)cc(Cl)n1
Reaction #275210
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1cc(C)nc(Cl)c1
Reaction #294206
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cc(C(=O)N(C)C)cc(Cl)n1
Reaction #328881
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cc1cc(C(=O)O)ccn1
Reaction #360270
6-methylpyridine-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CCOC(=O)c1cc(C)nc(Cl)c1
Reaction #366752
ethyl 2-chloro-6-methyl-4-pyridinecarboxylate
المردود 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
COC(=O)c1cc(C)nc(Cl)c1
Reaction #366792
methyl 2-chloro-6-methyl-pyridine-4-carboxylate
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1cc(C(=O)Nc2cccc(Oc3ccc4nc(NC(=O)C5CC5)cn4n3)c2)cc(Cl)n1
Reaction #404228
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1cc(C(=O)O)cc(N)n1
Reaction #489644
2-amino-6-methylisonicotinic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
Cc1cc(CO)cc(Cl)n1
Reaction #513294
pale yellow solid
المردود 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
Cc1cc(CO)cc(Cl)n1
Reaction #530464
2-chloro-4-hydroxymethyl-6-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_04
Cc1cc(C(=O)O)cc(N)n1
Reaction #676802
2-amino-6-methylisonicotinic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
Cc1cc(CO)cc(Cl)n1
Reaction #749917
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Cc1cc(CO)cc(Cl)n1
Reaction #751884
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Cc1cc(C(=O)O)cc(N2CCCC2)n1
Reaction #754159
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Cc1cc(C(=O)O)ccn1
Reaction #819183
6-methylpyridine-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
Cc1cc(C(=O)NC2CCc3ccccc32)cc(Cl)n1
Reaction #838979
المردود 14.8%AIChemEco amide coupling conditions 47k dataset
CCCN(C)C(=O)c1cc(C)nc(Cl)c1
Reaction #838986
المردود 30.1%AIChemEco amide coupling conditions 47k dataset
CSc1cccc(NC(=O)c2cc(C)nc(Cl)c2)c1
Reaction #838990
المردود 80.4%AIChemEco amide coupling conditions 47k dataset
CCCCN1CCN(C(=O)c2cc(C)nc(Cl)c2)CC1
Reaction #838994
المردود 39.8%AIChemEco amide coupling conditions 47k dataset
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