مشارك في 840 تفاعل

13945

CC(=O)[n+]1c(-c2ccco2)c(NC2CCCCC2)n2ccccc21.Cl.[Cl-]
Reaction #7630
1-acetyl-3-cyclohexylamino-2-furan-2-yl-imidazo[1,2-a]pyridin-1-ium chloride hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc(NC(=O)c2oc3cccnc3c2NC(=O)[C@H]2CC[C@H](N3CCOCC3=O)CC2)nc1
Reaction #44970
title compound
المردود 61.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(NC(=O)C(C)(C)C)nc1
Reaction #46225
2,2-dimethyl-N-(5-methyl-pyridin-2-yl)-propionamide
المردود 98.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc2nc(C)c(NC(C)(C)CC(C)(C)C)n2c1
Reaction #51080
Compound ( 17 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
[C-]#[N+]CCCCCCNc1c(-c2ccc(OC)c(OC)c2)nc2ccc(C)cn12
Reaction #51083
Compound ( 20 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1ccc(N2C(=O)c3nccnc3C2=O)nc1
Reaction #55356
6-(5-methylpyrid-2-yl)-5,7-dioxo-6,7-dihydro-5H-pyrrolo-[3,4-b]pyrazine
المردود 66.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCN(CC)CC.Cc1ccc(NC(=S)S)nc1
Reaction #56181
5-methyl-2-pyridyldithiocarbamic acid triethylamine salt
المردود 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
Cc1ccc2nc(-c3ccc(C(F)(F)F)cc3)cn2c1
Reaction #63796
6-Methyl-2-(4-trifluoromethylphenyl)imidazo[1,2-a]-pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCOC(=O)c1ccc(-c2cn3cc(C)ccc3n2)cc1
Reaction #63797
Ethyl 4-(6-methylimidazo[1,2-a]pyrid-2-yl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
Cc1ccc2nc(-c3ccc([N+](=O)[O-])cc3)cn2c1
Reaction #63798
6-Methyl-2-(4-nitrophenyl)imidazo[1,2-a]pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
Cc1ccc(NC(=O)C2(c3ccc4c(c3)OC(F)(F)O4)CC2)nc1
Reaction #67729
product
المردود 48.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1cnc(N)c([N+](=O)[O-])c1
Reaction #81872
38
المردود 25.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1ccc(-n2cc3cc(C4CC4)c([N+](=O)[O-])cc3n2)nc1
Reaction #91810
( ii )
المردود 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(NC(=O)C(CCO)Oc2ncnc3c2cnn3-c2ncccc2Cl)nc1
Reaction #190724
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(=O)Nc1ccc(C)cn1
Reaction #195507
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCCC(OC(C)=O)C(=O)Nc1ccc(C)cn1
Reaction #224358
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(NC(=O)C(O)C(C)C)nc1
Reaction #244643
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COCc1cc2c(Oc3ccc(S(C)(=O)=O)cc3)cc(C(=O)Nc3ccc(C)cn3)cc2o1
Reaction #245561
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(NC(=O)c2cc(Oc3ccc(S(C)(=O)=O)cc3)c3cc(C)oc3c2)nc1
Reaction #251153
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(NC(=O)c2cc(Oc3ccc(S(C)(=O)=O)cc3)c3c(c2)C(=O)N(C)C3)nc1
Reaction #274023
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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