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CC1CCNCC1

CC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccc(C(F)(F)F)c2)cc1
Reaction #2582
title compound
Ausbeute 101.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)N=C(N1CCC(C)CC1)c1cccc3c1N2CC3
Reaction #4111
9-Methyl-6-(4-methyl-1-piperidinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCN(C2=Nc3cc(Br)ccc3N3CCc4cccc2c43)CC1
Reaction #4112
product
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)N=C(N1CCC(C)CC1)c1cccc3c1N2CC3
Reaction #4169
9-Methyl-6-(4-methyl-1-piperidinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCN(C2=Nc3cc(Br)ccc3N3CCc4cccc2c43)CC1
Reaction #4170
product
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCN(c2cc3nc(C(C)(C)C)sc3cc2[N+](=O)[O-])CC1
Reaction #5881
2-tert-butyl-5-(4-methylpiperidin-1-yl)-6-nitrobenzothiazole
DOI: 10.6084/m9.figshare.5104873.v1
C#CCN1CCC(C)CC1
Reaction #6887
oil
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N1CCC(C)CC1
Reaction #7309
product
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCN(CCOc2cccc(-c3noc4ccsc34)c2)CC1
Reaction #8774
title compound
Ausbeute 96.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCC1CCN(CCOc2cccc(-c3noc4ccsc34)c2)CC1
Reaction #8775
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCN(c2nc(Nc3cc(C4CC4)n[nH]3)c3ccccc3n2)CC1
Reaction #11925
solid
Ausbeute 86.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(NC23N=CN=C2C=NC(N2CCC(C)CC2)=N3)[nH]n1
Reaction #11929
solid
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(Nc2ccc(Cl)c(C(F)(F)F)c2)nc2cc(OC3(C4CCNC(CCNC=O)C4)C=CC=CN3)ccc21
Reaction #41750
4-(2-{[4-chloro-3-trifluoromethylphenyl]amino-1-methylbenzimidazol-5-yloxy)(2-pyridyl)]-N-(2-piperidylethyl)carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC#CCOc1cc(N2CCC(C)CC2)ncn1
Reaction #42805
4-(2-butynyloxy)-6-(4-methylpiperidino) pyrimidine
Ausbeute 84.1%DOI: 10.6084/m9.figshare.5104873.v1
C#CCN1CCC(C(=O)OC)CC1
Reaction #44337
1-Prop-2-ynyl-piperidine-4-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(=O)n(C(=O)NCC2CCN(CC(C)(C)C(=O)OCc3ccccc3)CC2)c2ccccc21
Reaction #44881
title compound
Ausbeute 67.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(C)CCN(C(=S)Nc2ccc(Cl)cc2)CC1
Reaction #48554
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCN(Cc2ccc3c(c2)cc(-c2ccc(Cl)c4c2C(=O)NC4)n3C(=O)OC(C)(C)C)CC1
Reaction #49308
4-chloro-7-[1-(tert-butoxycarbonyl)-5-(4-methylpiperidinomethyl)indol-2-yl]isoindolinone
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(C(C)C)CC1
Reaction #59062
ethyl-1-(methylethyl)piperidine-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(COCC1CCNCC1)c1ccncc1)c1ccc2c(Cl)c[nH]c2c1
Reaction #60693
title compound
Ausbeute 101.4%DOI: 10.6084/m9.figshare.5104873.v1
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