Impliqué dans 63 réactions

788907

Cc1ccn2c(NC3CCCCC3)c(-c3cccn3C)nc2n1
Reaction #51093
Compound ( 38 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
—
Reaction #72527
title products
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cn1cccc1C(=O)CCC(=O)O
Reaction #94767
3-(1-methyl-2-pyrrolylcarbonyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
Cn1cccc1C(=O)CCC(=O)O
Reaction #94790
3-(1-methyl-2-pyrrolylcarbonyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
Cn1cccc1C(=O)CCC(=O)O
Reaction #94814
3-(1-methyl-2-pyrrolylcarbonyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCNCc1cccn1C
Reaction #195350
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(Cl)nc(C)c1C(=O)NCCC(C)N1CCC(NC(CNCc2cccn2C)c2ccccc2)CC1
Reaction #289181
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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Reaction #328886
title products
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cn1cccc1-c1nc2cc(Br)cc(N)n2n1
Reaction #364248
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
O=c1[nH]ccc2sccc12
Reaction #381248
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cn1cccc1C=CC1=CC(=O)C(C)(C)O1
Reaction #446552
crystals
Rendement 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
C#CC(O)c1cccn1C
Reaction #515855
3-Hydroxy-3-(1-methyl-pyrrol-2-yl)-1-propyne
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
CCn1c(C)cc2ccccc21
Reaction #521744
1-ethyl-2-methyl-1H-indole
Rendement 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_08
CN1C=C[NH+](C)C1C=Cc1cccn1C.[I-]
Reaction #522754
title compound
Rendement 74.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_02
Cn1cccc1-c1nc2c(N[C@H]3[C@@H](C(N)=O)[C@@H]4C=C[C@H]3C4)c(Br)cnc2[nH]1
Reaction #679170
title compound
Rendement 60.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
Cn1cc(Br)cc1C=O
Reaction #716366
4-bromo-1-methyl-1H-pyrrole-2-carbaldehyde
Rendement 95.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
Cn1cccc1/C=C(\C#N)c1ccc(Cl)cc1
Reaction #733365
solid
Rendement 85.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
O=c1[nH]ccc2sccc12
Reaction #740590
VI
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_06
CCOC(OCC)c1ccc(C(=O)C=Cc2ccccn2)cc1
Reaction #741434
4-[3-(2-Pyridyl)-2-propenoyl]benzaldehyde Diethyl Acetal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_07
Cn1cc([N+](=O)[O-])cc1C=O
Reaction #743478
compound 22-1
Rendement 49.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
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