2-methylpentane

Cn1cnc(-c2ccccc2)c1-c1nc(C#N)c(N)o1
Reaction #60789
title compound
Rendement 135.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1ccc(-n2nc(C(C)(C)C)cc2N)cc1
Reaction #91635
3-tert-butyl-1-p-tolyl-1H-pyrazol-5-amine
Rendement 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(S(=O)(=O)N2CCOCC2)cc1-c1cnc(N)c(Cl)n1
Reaction #168678
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
OCCc1cccc(CN2CCC3(CC2)CNCCO3)c1F
Reaction #176871
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)C(=O)Oc1c(-c2c(F)ccc(F)c2Cl)c(=O)[nH]c2nccnc12
Reaction #186375
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(NC(=O)c2cc(F)cc(N3CCOCC3)c2)cc1Nc1ncnc(Cl)c1N
Reaction #188737
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1nc(Br)ncc1Br
Reaction #204259
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)NCCC(O)c1nccs1
Reaction #204841
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(CC(=O)Sc2ccccc2)cc1
Reaction #228872
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1OC1CCCN(C(=O)C2CCCN2C)C1
Reaction #232984
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)CCCOCCCc1c[nH]cn1
Reaction #234783
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)NC1CCN(c2ccc(N3CC(COc4ccon4)OC3=O)cc2F)C1
Reaction #237263
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)Cn1c(=O)n(C)c(=O)c2c(-c3ccsc3)c(Cc3ccccc3C(F)(F)F)sc21
Reaction #251777
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1cc(OCc2ccccc2)cc(OC2CCOCC2)c1
Reaction #254034
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C(=O)NC1(c2ccccc2)CCC(=O)CC1)c1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #257062
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1OC1CCCN(CC(=O)N(C)C)C1
Reaction #267126
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
c1ccc(C(c2ccccc2)N2CC3(CNCCO3)C2)cc1
Reaction #273987
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc2ncnc(Nc3cc(NC(=O)c4ccccc4)c(Cl)cc3F)c2cc1OC
Reaction #274908
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1ccc(C)c(-n2cnc3ccc(C=O)cc3c2=O)c1
Reaction #276265
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
[Cl-]
Reaction #283481
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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