An 21 Reaktionen beteiligt

7309715

CC1CCCN1CCC1CN(C)C(=O)c2cccnc2O1
Reaction #4934
clear oil
Ausbeute 36.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)O.CC1CCCN1CCC1CN(C)C(=S)c2cccnc2O1.O=C(O)/C=C/C(=O)O
Reaction #4947
yellow crystals
Ausbeute 32.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC1CCCN1CCc1nc2cc(-c3ccc(C#N)cc3)ccc2o1
Reaction #10503
racemic 4-{2-[2-(2-methyl-pyrrolidin-1-yl)-ethyl]-benzooxazol-5-yl}-benzonitrile
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC1CCCN1c1ccc(C(=O)c2sc(Nc3ccc(N4CCN(C)CC4)cc3)nc2N)cc1[N+](=O)[O-]
Reaction #10904
racemic [4-Amino-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-5-thiazolyl][3-nitro-4-(2-methyl-1-pyrrolidinyl)phenyl]methanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC#CCOc1cc(N2CCCC2C)ncn1
Reaction #42808
4-(2-butynyloxy)-6-(2-methyl-pyrrolidin-1-yl) pyrimidine
Ausbeute 89.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(Cl)cc1-c1ccc(C(=O)N2CCCC2C)c(Cl)c1
Reaction #44369
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1CCCN1S(=O)(=O)c1ccc(-c2cccc(NC(=O)C3(c4ccc5c(c4)OCO5)CC3)n2)cc1
Reaction #46236
1-(Benzo[d][1,3]dioxol-5-yl)-N-(6-(4-(2-methylpyrrolidin-1-ylsulfonyl)phenyl)pyridin-2-yl)cyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1CCCN1C(C)(C)C#N
Reaction #49084
title compound
Ausbeute 37.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1CCCN1C1(C#N)CCCC1
Reaction #49096
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCCNCCOC
Reaction #78277
bis-(2-methoxyethyl)amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)N2CCCC2C)cn1
Reaction #170523
title compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc(CN5CCCC5C)c4)cc23)CC1
Reaction #177642
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CCCN1c1ccc(C(=O)O)nc1OCC1CC1
Reaction #181143
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CCCN1c1nc(Cl)nc2c1COC2c1ccc(F)cc1
Reaction #183455
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CCCN1CCc1cc2cc(-c3ccc(C(=O)N4CCOCC4)cn3)ccc2o1
Reaction #189811
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CCCN1CCc1cc2cc(-c3ccc(C#N)cc3)ccc2o1
Reaction #191996
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)c1ccc(N2CCCC2C)c2ccccc12
Reaction #204545
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CCCN1CCCOc1ccc2c(c1)cc1n2CCNC1=O
Reaction #207694
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CN(C(=O)OC(C)(C)C)CCN1c1cc(-c2ccc(F)cc2)nc(N2CCCC2C)n1
Reaction #212529
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CCCN1C(=O)c1ccc(C(=O)NCc2nc3cc(Cl)ccc3[nH]2)cc1Cl
Reaction #221606
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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