cyclobutylamine

Clc1cccnc1NC1CCC1
Reaction #650
Ausbeute 25.0%750 AstraZeneca ELN dataset
CS(=O)(=O)c1ccc(NC2CCC2)c(C(=O)N2CCN(c3ccc(C(F)(F)F)cc3)CC2)c1
Reaction #61047
title compound
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(NC1CCC1)c1ccncc1Nc1ccc(I)cc1F
Reaction #67838
N-(cyclobutyl)-3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Brc1cnc(NC2CCC2)nc1
Reaction #68840
5-Bromo-N-cyclobutylpyrimidin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc2[nH]c3c(c2c1)CC1(C)C(=O)N(CCNC2CCC2)C(=O)N1C3c1cccc(O)c1
Reaction #69320
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(COc1cccc(-c2nc(Nc3ccc4[nH]ncc4c3)c3ccccc3n2)c1)NC1CCC1
Reaction #89874
2-(3-(4-(1H-indazol-5-ylamino)quinazolin-2-yl)phenoxy)-N-cyclobutylacetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1nc(NCc2ccccn2)nc(NC2CCC2)c1C
Reaction #91415
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCC(CC)Nc1nc(NCc2ccccn2)nc(C)c1C
Reaction #91416
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(NC1CCC1)C(O)c1ccc(-c2noc(-c3onc(-c4ccccc4)c3C(F)(F)F)n2)cc1
Reaction #164416
(R/S)-N-cyclobutyl-2-hydroxy-2-(4-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetamide
Ausbeute 23.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(NC1CCC1)c1ccncc1Nc1ccc(I)cc1F
Reaction #166003
N-(cyclobutyl)-3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)c1cn(C2CCC2)cn1
Reaction #169485
1-cyclobutyl-1H-imidazole-4-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)NC2CCC2)cn1
Reaction #170319
title compound
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)c1nc2cc(S(=O)(=O)NC3CCC3)ccc2n1CC1CCOCC1
Reaction #175105
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(C(=O)NC2CCC2)cc1-n1cc(C)c2ccc(OCCCl)cc2c1=O
Reaction #176197
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Brc1cncc(NC2CCC2)c1
Reaction #177503
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)CNC1CCC1
Reaction #179807
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(NC1CCC1)c1ccccc1Nc1ccc2c(C=Cc3ccccn3)n[nH]c2c1
Reaction #184614
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(NC(=O)c2ccnc(NC3CCC3)c2)cc1-c1ccc(C(=O)NCC2CC2)cc1
Reaction #193412
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(NC1CCC1)c1cnc(Nc2cc(Cl)ccc2Cl)nc1C(F)(F)F
Reaction #193628
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1ccc(Oc2ccnc(NC3CCC3)n2)c2ccccc12)c1cc(F)cc(N2CCCCC2)c1
Reaction #204992
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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