1,3-dimethyl-2-imidazolidinone

Cc1ccc(-c2c(NS(=O)(=O)c3ccc(C(C)(C)C)cc3)ncnc2OCCOc2ncc(C#N)cn2)cc1
Reaction #2392
4-tert-butyl-N-{6-[2-(5-cyanopyrimidin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(OC(=O)c1nn(C)c2ccccc12)C1CCCCN1C
Reaction #5969
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COCCCc1nnc(-c2ccc(-c3ccccc3)nc2)n1-c1cccc(C(N)=O)c1C
Reaction #7024
compound
Ausbeute 56.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#Cc1ccc(CN=[N+]=[N-])cc1
Reaction #64198
4-azidomethylbenzonitrile
Ausbeute 96.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CN1Cc2cc(Br)ccc2C1=O
Reaction #68501
5-bromo-2-methylisoindolin-1-one
Ausbeute 57.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Fc1cc(Br)ccc1C(F)(F)C(F)(F)F
Reaction #70131
product
Ausbeute 75.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=c1[nH]c2ccc3nnc(C(F)F)n3c2cc1-c1ccccc1
Reaction #70655
1-(difluoromethyl)-8-phenyl[1,2,4]triazolo[4,3-a]-1,5-naphthyridin-7(6H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CN1CCN(C)C1=NC(c1ccccc1)c1ccccc1
Reaction #74917
1,3-dimethyl-2-diphenylmethyliminoimidazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
CC(=O)c1ccc(Nc2nnc(Cc3ccncc3)c3ccccc23)cc1O
Reaction #78185
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cl.O=[N+]([O-])c1ccc(CCNC[C@H](O)c2ccccc2)cc1
Reaction #163205
(R)-2-[[2-(4-nitrophenyl)ethyl]amino]-1-phenylethanol monohydrochloride
Ausbeute 90.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1ccccc1NC(=O)c1ccc(CNC(=O)OCc2cccnc2)cc1
Reaction #174684
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Fc1cnc2[nH]ccc2c1NC1CCCCC1
Reaction #202920
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)c1cccc(C(C)(C)C)c1OS(C)(=O)=O
Reaction #204669
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCc1ccccc1N=CN1CCNC1=N[N+](=O)[O-]
Reaction #207681
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[Cl-]
Reaction #211805
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1ccc(F)c(F)c1O
Reaction #213407
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1ccc(-c2cc3c(Oc4ccc5[nH]c(C)cc5c4F)ncnc3[nH]2)cc1
Reaction #220236
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC1OC(Cn2cncn2)(c2ccc(Cl)cc2)C1C
Reaction #233705
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NC(=S)c1cccc(C2=Nc3ccc(-c4ccc(F)cc4)cc3NC(=O)C2)c1
Reaction #241733
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CSc1ccc(C(=O)OC2CCCC2)cc1OC1CCCC1
Reaction #247334
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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