pyridinone

CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #1603
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)cnc1=O
Reaction #1607
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #1670
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)cnc1=O
Reaction #1675
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #2175
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)cnc1=O
Reaction #2180
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #2216
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)cnc1=O
Reaction #2221
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #2274
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)cnc1=O
Reaction #2279
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1cc(OCc2ccc(Cl)cn2)ccn1-c1ccc(OC[C@H]2CCCN2)cc1
Reaction #43362
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCN1CCC[C@H]1COc1ccc(-n2ccc(OCc3ccc(Cl)cn3)cc2=O)cc1
Reaction #43364
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)Cn1ccccc1=O
Reaction #47094
product 425
Rendimiento 76.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1c(-c2ccccc2)c[n+](C)cc1-c1cccc(Br)c1.O=S(=O)([O-])C(F)(F)F
Reaction #74860
3-(3-bromophenyl)-4-methoxy-1-methyl-5-phenylpyridinium trifluoromethanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
COc1c(-c2ccccc2)c[n+](C)cc1-c1cccc(Br)c1.CS(=O)(=O)[O-]
Reaction #74862
5-(3-bromophenyl)-4-methoxy-1-methyl-3-phenylpyridinium methanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
Cc1cc(C2CCCCC2)c(CNC(=O)c2cc(Br)cc3c2cnn3C(C)C)c(=O)[nH]1
Reaction #172636
solution
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COCC(=O)CC(=O)C(=CN(C)C)c1cccc(C(F)(F)F)c1
Reaction #201383
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1nc(-n2ccccc2=O)sc1C(=O)NCc1ccc(F)cc1
Reaction #202738
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)C(=O)Oc1ccc(Cn2ccccc2=O)cc1Cl
Reaction #258530
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)Oc1ccccn1
Reaction #294285
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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