An 454 Reaktionen beteiligt

17448

O=[N+]([O-])c1cnc2cc(Br)ccc2c1NCC1CCCCC1
Reaction #9557
(7-bromo-3-nitroquinolin-4-yl)cyclohexylmethylamine
Ausbeute 62.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(NCC1CCCCC1)C(c1cc(F)cc(F)c1)C1CN(C(c2ccc(Cl)cc2)c2ccc(Cl)cc2)C1
Reaction #46344
(RS)-2-{1-[bis(4-chlorophenyl)methyl]azetidin-3-yl}-2-(3,5-difluoro-phenyl)-N-cyclohexylmethylacetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1C(NCC2CCCCC2)=N[C@@H](c2ccccc2)[C@H]1c1ccccc1
Reaction #47005
product 79
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)n1c(-c2ccc(Cl)c3c2C(=O)NC3)cc2cc(CNCC3CCCCC3)ccc21
Reaction #49325
4-chloro-7-[1-(tert-butoxycarbonyl)-5-(cyclohexylmethylaminomethyl)indol-2-yl]isoindolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(NCC1CCCCC1)c1cccc(CS(=O)(=O)C=C2CN(C(c3ccc(Cl)cc3)c3ccc(Cl)cc3)C2)c1
Reaction #53495
3-({1-[bis(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)-N-cyclohexylmethylbenzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Nc1ncnc2sc(-c3c(-c4ccccc4)ncn3CC3CCCCC3)cc12
Reaction #60904
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
c1ccc(C2CCC(NCC3CCCCC3)CC2)cc1
Reaction #65573
N-(4-phenylcyclohexyl)-N-cyclohexylmethylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=C1N=C(NCC2CCCCC2)OC1c1ccccc1
Reaction #74370
2-[(cyclohexylmethyl)amino]-5-phenyl-1,3-oxazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C1N=C(NCC2CCCCC2)OC1Cc1ccccc1
Reaction #74372
5-benzyl-2-[(cyclohexylmethyl)amino]-1,3-oxazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(O)C1CCN(CC2CCCCC2)C1=O
Reaction #86855
1-(cyclohexylmethyl)-2-oxopyrrolidine-3-carboxylic acid
Ausbeute 86.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1nc(NCc2ccccn2)nc(NCC2CCCCC2)c1C
Reaction #91458
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
N#CCC(=O)NCC1CCCCC1
Reaction #177957
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(NCC1CCCCC1)c1ccc(C(c2cc(F)ccc2F)S(=O)(=O)c2ccc(Cl)cc2)nc1
Reaction #181178
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c(F)cccc1NC(=O)c1ccccc1CN1C(=O)C2(COc3cc4c(cc32)CCO4)c2ccccc21
Reaction #192564
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1ccccc1)c1ccc(CN2C(=O)C3(COc4cc5c(cc43)CCO5)c3ccccc32)cc1
Reaction #196151
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc2nc(NCC3CCCCC3)sc2c1
Reaction #206635
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCC(=O)NCC1CCCCC1
Reaction #207651
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1cc2[nH]ncc2cc1NC1CCC(NCC2CCCCC2)CC1
Reaction #213214
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1nc2c(o1)c(C(=O)NCC1CCCCC1)cc1nc(Nc3c(Cl)cccc3Cl)[nH]c12
Reaction #237304
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=[N+]([O-])c1cc(Oc2ccccc2)ccc1NCC1CCCCC1
Reaction #239630
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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