3-aminopyrazole

c1cnc2c(c1)CCCC2N(Cc1ccc(CNc2cc[nH]n2)cc1)Cc1nc2ccccc2[nH]1
Reaction #7276
amine
수율 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1c2ccccc2C(=O)N1c1cc[nH]n1
Reaction #47277
2-(1H-pyrazol-3-yl)-isoindole-1,3-dione
수율 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
NCCCNc1cc[nH]n1
Reaction #55781
3-(3-aminopropylamino)pyrazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
O=C(CCCCl)Nc1ccn(C(=O)CCCCl)n1
Reaction #61068
title compound
수율 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(NCCCCl)Nc1ccn(C(=O)NCCCCl)n1
Reaction #61069
title compound
수율 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(=O)Nc1cc[nH]n1
Reaction #61071
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(=O)Nc1cc[nH]n1
Reaction #66950
title compound
수율 49.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C1c2ccccc2C(=O)N1c1cc[nH]n1
Reaction #66952
title compound
수율 92.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC1=C(C(=O)OC(C)(C)C)C(C(C)C)n2nccc2N1
Reaction #77551
title compound
수율 41.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC1=C(C(=O)N2CCN(c3ccccc3)CC2)Cn2nccc2N1
Reaction #77552
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOC(=O)c1cc(O)nc2[nH]ncc12
Reaction #169202
title compound
수율 28.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(C)n1-c1cc[nH]n1
Reaction #170678
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1ccn(Cc2cc(F)c(F)c(F)c2)n1
Reaction #175175
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(C)CCCOc1ccc(Cc2cc(N)[nH]n2)cc1
Reaction #176819
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1Nc2ccc(Cl)cc2C1=CNc1cc[nH]n1
Reaction #182404
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1c2ccccc2C(=O)N1c1cc[nH]n1
Reaction #183180
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1[nH]nc(NC=C2C(=O)Nc3ccccc32)c1C#N
Reaction #190316
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=S(=O)(Cl)c1cc[nH]n1
Reaction #192121
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=Nc1cc[nH]n1)C1CCOC1=O
Reaction #198155
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)Nc1cc[nH]n1
Reaction #199029
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
1 페이지다음 페이지