nicotinic acid

O=C(NCCc1ccc(O)c(O)c1)c1cccnc1
Reaction #4668
N-nicotinoyldopamine
收率 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C(ON1C(=O)CCC1=O)c1cccnc1
Reaction #4674
N-Nicotinoyloxysuccinimide
收率 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
—
Reaction #5107
nicotinate ester
收率 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cl.O=C(Cl)c1cccnc1
Reaction #70898
Nicotinoyl chloride hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(c1cccnc1)N1CCN(S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #71667
title compound
收率 46.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
—
Reaction #72725
solid
收率 9.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)C1=C(COCCN)NC(C)=C(C(=O)OC)C1c1ccccc1Cl.O=C([O-])c1cccnc1
Reaction #75876
amlodipine nicotinate
收率 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
C[C@H](NC(=O)c1cccnc1)C(=O)OC(C)(C)C
Reaction #83171
nicotinoyl-alanine t-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOCc1nc2c(N)nc3ccccc3c2n1CC(C)(C)OCCNC(=O)c1cccnc1
Reaction #91973
title product
收率 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(Nc1cnn2ccc(N3CCC[C@@H]3c3cccc(F)c3)nc12)c1cccnc1
Reaction #92302
final product
收率 74.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(Nc1c[nH]c2nccc(N3CCN(Cc4ccccc4)CC3)c12)c1cccnc1
Reaction #166772
N-(4-(4-benzylpiperazin-1-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl)nicotinamide
收率 59.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(Nc1c[nH]c2ncc(Br)c(F)c12)c1cccnc1
Reaction #166796
N-(5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)nicotinamide
收率 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCc1cn(-c2ccc3ncsc3c2)c(=O)n1-c1cccnc1
Reaction #167405
product
收率 1.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)C(N)(C(=O)c1cccnc1)C(C)C
Reaction #169658
required product
收率 369.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCC(C)C(NC(=O)c1cccnc1)C(=O)OC
Reaction #169662
product
收率 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)CCC(N)(C(=O)OC)C(=O)c1ccccc1
Reaction #169664
required product
收率 97.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=CCc1ccc(OC(=O)CC(OC(=O)c2cccnc2)C(=O)OC)c(OC)c1
Reaction #169669
oil
收率 58.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)C1CCCN1C(=O)c1cccnc1
Reaction #169670
product
收率 172.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=CCc1ccc(OC(=O)CNC(=O)c2cccnc2)c(OC)c1
Reaction #169674
product
收率 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)C(N)(CC(C)C)C(=O)c1cccnc1
Reaction #169679
required product
收率 72.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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