cyclopentylmethanamine

Cc1nc(NCc2ccccn2)nc(NCC2CCCC2)c1C
Reaction #91412
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C#CCOc1ccc(C(=O)NCC2CCCC2)cc1OC
Reaction #194554
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C(C)C)cc1-c1cnc2[nH]c(=O)n(C(C)C3CCCC3)c2n1
Reaction #196924
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(NCC1CCCC1)c1ccc(N2CC3=C(CN(C(=O)c4ccccc4C(F)(F)F)C3)C2)nc1
Reaction #204153
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(NCC1CCCC1)c1ccc2[nH]ccc2c1
Reaction #211030
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(NCC1CCCC1)c1ccc2cc[nH]c2c1
Reaction #221144
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(NCC1CCCC1)c1cnc(Nc2ccccc2)nc1C(F)(F)F
Reaction #224122
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(c1ccc(NCC2CCCC2)c([N+](=O)[O-])c1)N(CC(F)(F)F)CC(F)(F)F
Reaction #264358
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
c1ccc2c(CNCC3CCCC3)c3ccccc3cc2c1
Reaction #267636
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(NCC1CCCC1)OCc1ccccc1
Reaction #273865
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(NCC1CCCC1)NC1CCN(CC23CC(c4ccccc42)c2ccccc23)CC1
Reaction #345483
title compound
Yield 35.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
N#CC1CC(F)CN1C(=O)CNC12CCC(C(=O)NCC3CCCC3)(CC1)CC2
Reaction #392464
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(Cc1ccc2cc[nH]c2c1)NCC1CCCC1
Reaction #417322
N-cyclopentylmethylindole-6-acetamide
Yield 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_01
O=C(NCC1CCCC1)OCc1ccccc1
Reaction #452559
N-Cbz-cyclopentylmethylamine
Yield 121.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
COc1ccc(C(C)C)cc1-c1cnc2[nH]c(=O)n(C(C)C3CCCC3)c2n1
Reaction #475271
solid
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CN=C1SCC(O)(c2ccc(Cl)c(S(=O)(=O)NCC3CCCC3)c2)N1C
Reaction #548356
4-(4-Chloro-3-cyclopentylmethylsulfamoylphenyl)-3-methyl-2-methylimino-1,3-thiazolidine-4-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_12
C#CCOc1ccc(C(=O)NCC2CCCC2)cc1OC
Reaction #689163
N-cyclopentylmethyl-4-(2-propynyloxy)-3-methoxybenzamide
Yield 80.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
C#CCOc1c(OC)cc(OC)cc1C(=O)NCC1CCCC1
Reaction #689170
N-cyclopentylmethyl-3,5-dimethoxy-(2-propynyloxy)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
C#CCOc1c(F)cc(C(=O)NCC2CCCC2)cc1F
Reaction #689180
N-cyclopentylmethyl-3,5-difluoro-4-(2-propynyloxy)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
C#CCOc1c(F)cc(C(=O)NCC2CCCC2)cc1F
Reaction #769533
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
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