#5944600

CN(C)C1CCN(C(N)=S)C1
Reaction #7914
3-dimethylamino-pyrrolidine-1-carbothioic acid amide
Ausbeute 23.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(CCc2cc(NC(=O)c3cnc(N4CCC(N(C)C)C4)cn3)[nH]n2)cc(OC)c1
Reaction #45146
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(Nc1ncnc2cc(C(=O)N3CCC(N(C)C)C3)c(Cl)cc12)c1nc2cc(Cl)ccc2[nH]1
Reaction #62477
6-chloro-4-[(1R/S)-1-(5-chloro-1H-benzimidazol-2-yl)-ethylamino]-7-[(3R/S)-3-dimethylamino-pyrrolidin-1-yl-carbonyl]-quinazoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CN(C)C1CCN(C(N)=S)C1
Reaction #75558
3-dimethylamino-pyrrolidine-1-carbothioic acid amide
Ausbeute 23.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CN(C)C1CCN(c2ccc([N+](=O)[O-])cc2Cl)C1
Reaction #156589
[1-(2-Chloro-4-nitrophenyl)pyrrolidin-3-yl]dimethylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cc(N2CCC(N(C)C)C2)ccc1[N+](=O)[O-]
Reaction #159376
Dimethyl-[1-(3-methyl-4-nitrophenyl)pyrrolidin-3-yl]amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CN(C)C1CCN(C(=O)c2ccc(N)cc2)C1
Reaction #179145
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1cc(O)c(F)cc1-c1ccc2c(-c3nc4c([nH]3)CCN(C(=O)c3cnc(N5CCC(N(C)C)C5)cn3)C4)n[nH]c2c1
Reaction #179462
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c(-c2ccccc2)c(N2CCC(N(C)C)C2)c2oc(N(C)CCCC(=O)N(C)C)nc2c1C#N
Reaction #181209
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c(-c2ccccc2)c(N2CCC(N(C)C)C2)c2oc(C(C)(C)C(N)=O)nc2c1C#N
Reaction #187108
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CNC(=O)c1nc2c(C#N)c(C)c(-c3ccccc3)c(N3CCC(N(C)C)C3)c2o1
Reaction #190739
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1nc2ccc(N3CCC(N(C)C)C3)cc2c(-c2ccc(F)cc2)c1C(=O)C(F)(F)F
Reaction #190948
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c(-c2ccccc2)c(N2CCC(N(C)C)C2)c2oc(-c3cnccn3)nc2c1C#N
Reaction #198062
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c(-c2ccccc2)c(N2CCC(N(C)C)C2)c2oc(C(=O)N(C)CCc3ccccc3)nc2c1C#N
Reaction #199959
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(C)C1CCN(C(=O)c2ccc3c(c2)-c2sc(-c4ncnn4-c4ccc(F)cc4F)cc2CCO3)C1
Reaction #201290
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c(-n2cccc2)c(N2CCC(N(C)C)C2)c2oc(C3CC3)nc2c1C#N
Reaction #202895
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1cc(OC)cc2nc(-c3cccnc3N3CCC(N(C)C)C3)oc(=O)c12
Reaction #204902
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(C)C1CCN(c2cc(NC(=O)c3ccc(C(C)(C)O)cc3)nc3ccnn23)C1
Reaction #207519
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CCCNc1nc2c(C#N)c(C)c(-c3ccccc3)c(N3CCC(N(C)C)C3)c2o1
Reaction #208733
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c(-c2ccccc2)c(N2CCC(N(C)C)C2)c2oc(N(C)C(C)(C)C)nc2c1C#N
Reaction #209985
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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