مشارك في 196 تفاعل

14734

Cl.N=C(N)c1ccncc1
Reaction #8691
4-Amidino-pyridine hydrochloride
المردود 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cl.N=C(N)c1ccncc1
Reaction #10333
4-Amidino-pyridine hydrochloride
المردود 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Nc1ccc(Cl)cc1C(=O)c1ccncc1
Reaction #57777
(2-amino-5-chloro-phenyl)-pyridin-4-yl-methanone
المردود 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Nc1cc(F)c(F)cc1C(=O)c1ccncc1
Reaction #57785
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CSc1nc(-c2ccncc2)c(-c2ccc3ccccc3c2)c(=O)n1C
Reaction #62241
3-Methyl-2-methylsulfanyl-5-naphthalen-2-yl-6-pyridin-4-yl-3H-pyrimidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
c1ccc(-c2ncc(-c3cnc(-c4ccncc4)[nH]3)cn2)cc1
Reaction #70562
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CS(=O)(=O)c1ccc(NC(=N)c2ccncc2)cc1
Reaction #80620
N-[4-(methylsulfonyl) phenyl]-4-pyridinecarboximidamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1ccccc1C(=O)c1ccncc1
Reaction #83271
2-isonicotinoyltoluene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
[Cl-]
Reaction #181690
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C(=O)c2ccncc2)c1
Reaction #198086
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C[Si](C)(C)C#Cc1ccncc1
Reaction #202871
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(NC(=N)c2ccncc2)cc1
Reaction #202890
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1cc(-c2nc(-c3cnccn3)n[nH]2)ccn1
Reaction #214884
3-pyrazinyl-5-(4-pyridyl)-1,2,4-triazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
Nc1ccc(-c2n[nH]c(-c3ccncc3)n2)cc1
Reaction #214888
3-(p-aminophenyl)-5-(4-pyridyl)-1,2,4-triazole
المردود 20.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
COc1ccc(C(=O)c2ccncc2)cc1OC
Reaction #222495
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OC(c1ccccc1)(c1ccccc1)c1ccncc1
Reaction #254849
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOc1ccc(NC(=N)c2ccncc2)cc1
Reaction #254859
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NC(=O)c1ccncc1
Reaction #279861
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc(N)c(C(=O)c2ccncc2)cc1OC
Reaction #286485
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
N#Cc1ccnc(CO)c1
Reaction #294415
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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