iodocyclopentane

O=[N+]([O-])c1ccc(N2CCN(C3CCCC3)CC2)cc1
Reaction #10887
1-cyclopentyl-4-(4-nitrophenyl)piperazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
OC[C@H]1O[C@](O)(c2ccc(Cl)c(Cc3ccc(OC4CCCC4)cc3)c2)[C@H](O)[C@@H](O)[C@@H]1O
Reaction #48104
1-Chloro-2-(4-cyclopentyloxybenzyl)-4-(β-D-glucopyranos-1-yl)-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(OC3CCCC3)cc2n1Cc1ccccc1
Reaction #68321
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)c1c(C(=O)NCc2ccc(C(F)(F)F)nc2)c2ccc(OC3CCCC3)cc2n1Cc1ccccn1
Reaction #68412
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)c1c(C(=O)NCc2cncc(F)c2)c2ccc(OC3CCCC3)cc2n1Cc1cccnc1
Reaction #68419
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1cc(Cl)c(OC2CCCC2)c(OC2CCCC2)c1
Reaction #91008
methyl 3-chloro-4,5-bis(cyclopentyloxy)benzoate
Ausbeute 85.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Nc1ccc2c(C3CCCC3)c[nH]c2c1
Reaction #161117
3-Cyclopentyl-1H-indol-6-ylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1cc(Br)cc2c1cnn2C1CCCC1
Reaction #172641
methyl 6-bromo-1-cyclopentyl-1H-indazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
OCC1OC(O)(c2ccc(Cl)c(Cc3ccc(OC4CCCC4)cc3)c2)C(O)C(O)C1O
Reaction #183642
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)c1c(C(=O)NCc2ccc(C(F)(F)F)nc2)c2ccc(OC3CCCC3)cc2n1Cc1ccccn1
Reaction #234633
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)c1cn(C2CCCC2)nc1-c1ccc(Oc2ccccc2)cc1
Reaction #234764
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#Cc1ccc(Oc2ccc3c(c2)COB3O)c(OC2CCCC2)c1
Reaction #242429
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)NC1CCN(C2CCCC2)CC1
Reaction #242962
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=[N+]([O-])c1ccc(N2CCN(C3CCCC3)CC2)cc1
Reaction #277844
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Brc1ccc(OC2CCCC2)cn1
Reaction #285533
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)NC1CCN(C2CCCC2)C1
Reaction #286812
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1cc(-c2ccccn2)c(=O)n(C2CCCC2)c1
Reaction #291166
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)NC1CCN(C2CCCC2)CC1
Reaction #307390
(1-Cyclopentyl-piperidin-4-yl)-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COc1cc(F)cc(-c2nn(C3CCCC3)c3ncnc(N)c23)c1
Reaction #325192
1-cyclopentyl-3-(3-fluoro-5-methoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Nc1ncnc2c1c(I)nn2C1CCCC1
Reaction #325193
1-cyclopentyl-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
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