Participa en 306 reacciones

40336

CC(C)(C)OC(=O)n1c(-c2ccc(Cl)c3c2C(=O)NC3)cc2cc(CN3CCN(c4ncccn4)CC3)ccc21
Reaction #49338
4-chloro-7-(1-(tert-butoxycarbonyl)-5-[4-(pyrimidin-2-yl)piperazin-1-ylmethyl]indol-2-yl)isoindolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(C(=O)Nc2c(NC(=O)CN3CCN(c4ncccn4)CC3)ccc3c2C(=O)c2ccccc2C3=O)cc1
Reaction #69060
1-(4-methylbenzamido)-2-[2-[4-(2-pyrimidinyl)piperazino]acetylamino]-anthraquinone
Rendimiento 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ccc(SCc2cnc(NC(=O)c3ccc(C(C)(C)C)cc3)s2)cc1C(=O)N1CCN(c2ncccn2)CC1
Reaction #77423
desired product
Rendimiento 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(CBr)N1CCN(c2ncccn2)CC1
Reaction #155735
desired compound
Rendimiento 0.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cc(-c2cc(-c3ccccc3)n(CC(=O)N3CCN(c4ncccn4)CC3)n2)ccc1F
Reaction #155744
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(Cn1nc(-c2ccccc2)cc1-c1ccccc1)N1CCN(c2ncccn2)CC1
Reaction #155745
desired compound
Rendimiento 73.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(Cn1c(Br)nc(Br)c1Br)N1CCN(c2ncccn2)CC1
Reaction #171952
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(Cn1cc(-c2ccccc2)nc1-c1ccccc1)N1CCN(c2ncccn2)CC1
Reaction #171955
desired product
Rendimiento 48.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(c1cccc(-c2cnc3c(c2)N(Cc2cc(Cl)ccc2C(F)(F)F)CCN3)c1)N1CCN(c2ncccn2)CC1
Reaction #173515
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cl
Reaction #174386
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1cnc(N2CCN(CCCOc3ccc(-c4csc5ccccc45)cc3)CC2)nc1
Reaction #178987
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1cccc2cc[nH]c12)N1CCN(c2ncccn2)CC1
Reaction #185245
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCC(C(=O)OCC)N1CCN(c2ncccn2)CC1
Reaction #191315
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[Br-]
Reaction #192572
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1ccc2nc(CN3CCN(c4ncccn4)CC3)cn2c1
Reaction #192580
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=c1nc(CN2CCN(c3ncccn3)CC2)[nH]c2ccccc12
Reaction #213590
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NS(=O)(=O)c1cc2c(c(C(=O)N3CCN(c4ncccn4)CC3)c1)OCCO2
Reaction #214582
1-(2,3-ethylenedioxy-5-sulfamoylbenzoyl)-4-(2-pyrimidinyl)-piperazine
Rendimiento 40.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
O=[N+]([O-])c1ccc(N2CCN(c3ncccn3)CC2)nc1
Reaction #221332
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(SCc2cnc(NC(=O)c3ccc(C(C)(C)C)cc3)s2)cc1C(=O)N1CCN(c2ncccn2)CC1
Reaction #221711
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1nc2ccc(Cl)cc2nc1NC(=O)N1CCN(c2ncccn2)CC1
Reaction #232025
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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