Participa en 612 reacciones

1237785

CC(=O)O.CC(=O)O.CC(=O)O.COc1cc(-c2csc3c(C(=O)NCC4CCCN4CC(N)=O)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45457
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCn1nc(C(C)C)c(O)c(C2=Nc3ccc(OCC(N)=O)cc3S(=O)(=O)N2)c1=O
Reaction #59251
desired product ( 5g )
Rendimiento 49.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
NC(=O)CN1Cc2ncnc(Oc3ccc4c(ccn4C(=O)Nc4cccc(C(F)(F)F)c4)c3)c2C1
Reaction #73379
5-(6-carbamoylmethyl-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-4-yloxy)-indole-1-carboxylic acid (3-trifluoromethyl-phenyl)-amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
NC(=O)CN1CCC(c2noc3cc(F)ccc23)CC1
Reaction #83970
white crystals
Rendimiento 33.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
NC(=O)COc1cccc(F)c1
Reaction #84556
title compound
Rendimiento 30.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
NC(=O)COc1cccc(Cl)c1
Reaction #84559
title compound
Rendimiento 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
N#Cc1cccc(OCC(N)=O)c1
Reaction #84561
title compound
Rendimiento 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
NC(=O)COc1cccc(F)c1
Reaction #84563
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
NC(=O)COc1ccc(Cl)c2ccccc12
Reaction #84568
title compound
Rendimiento 49.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C#Cc1cccc(OCC(N)=O)c1
Reaction #84570
title compound
Rendimiento 90.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
N#Cc1cccc(OCC(N)=O)c1
Reaction #84578
title compound
Rendimiento 28.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1cccc(OCC(N)=O)c1
Reaction #84580
title compound
Rendimiento 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cn1cc(Br)c(=O)n(CC(N)=O)c1=O
Reaction #86320
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC1(C)c2cc(OCC(N)=O)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Reaction #90001
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(C)c(-c2nc3c(c(N4CCN(CC(N)=O)C[C@H]4C)n2)CN(c2cc(C(C)C)ccc2C)CC3)c1
Reaction #167959
(R)-2-(4-(2-(2,5-dimethylphenyl)-6-(5-isopropyl-2-methylphenyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-yl)-3-methylpiperazin-1-yl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1c[nH]c2cccc(-c3nc4c(c(N5CCN(CC(N)=O)[C@H](C)C5)n3)CN(c3cc(C(C)C)nn3C)CC4)c12
Reaction #167993
(R)-2-(4-(6-(3-isopropyl-1-methyl-1H-pyrazol-5-yl)-2-(3-methyl-1H-indol-4-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-yl)-2-methylpiperazin-1-yl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cccc(C)c1-c1nc2c(c(N3CCN(CC(N)=O)[C@H](C)C3)n1)CN(c1cc(C(C)C)nn1C)CC2
Reaction #167994
(R)-2-(4-(2-(2,6-dimethylphenyl)-6-(3-isopropyl-1-methyl-1H-pyrazol-5-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-yl)-2-methylpiperazin-1-yl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
NC(=O)Cn1cc(C(=O)c2cncc(NC(=O)Cc3ccc(Cl)cc3)c2)c2cncnc21
Reaction #169286
title compound
Rendimiento 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
NC(=O)CN1C(=O)c2ccc(OCc3ccc(F)cc3)cc2C1=O
Reaction #189170
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(C)OB(c2cnn(CC(N)=O)c2)OC1(C)C
Reaction #189184
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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