An 228 Reaktionen beteiligt

20172

CCOC(=S)SCc1ccccn1
Reaction #52576
Carbonodithioic Acid, O-ethyl S-(2-pyridinylmethyl) Ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COC(=O)Nc1nc2c(OC)ccc(NCc3ccccn3)c2s1
Reaction #80136
{4-methoxy-7-[(pyridin-2-ylmethyl)-amino]-benzothiazol-2-yl}-carbamic acid methyl ester
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(N(C)Cc2ccccn2)c2sc(NC(=O)c3ccc(F)cc3)nc12
Reaction #80149
4-Fluoro-N-[4-methoxy-7-(methyl-pyridin-2-ylmethyl-amino)-benzothiazol-2-yl]-benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOC(=O)C(Cc1ccccn1)n1ccc(-c2cc(Cl)ccc2C(F)(F)F)cc1=O
Reaction #84952
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=S(=O)(Nc1cc(Cl)ccc1SCc1ccccn1)c1cc2ccccc2o1
Reaction #157579
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1c(Cl)c(C)c(C(C)=O)c(OCc2ccccn2)c1OCCC(C)c1ccc(F)cc1
Reaction #306639
title compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
—
Reaction #314121
pale yellow solid
Ausbeute 29.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Cc1cccc(C(=O)c2cn(Cc3ccccn3)c3ccccc3c2=O)c1
Reaction #314127
pale yellow solid 4w
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Cc1ccc(C(=O)c2cn(Cc3ccccn3)c3cc4c(cc3c2=O)OCO4)cc1C
Reaction #314281
7-(3,4-dimethyl-benzoyl)-5-pyridin-2-ylmethyl-5H-[1,3]dioxolo[4,5-g]quinolin-8-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Cc1ccc(C(=O)c2cn(Cc3ccccn3)c3cc4c(cc3c2=O)OCCO4)cc1C
Reaction #314284
8-(3,4-Dimethyl-benzoyl)-6-pyridin-2-ylmethyl-2,3-dihydro-6H-[1,4]dioxino[2,3-g]quinolin-9-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Cc1ccc(C(=O)c2cn(Cc3ccccn3)c3ccc(C(F)(F)F)cc3c2=O)cc1C
Reaction #314292
3-(3,4-Dimethyl-benzoyl)-1-pyridin-2-ylmethyl-6-trifluoromethyl-1H-quinolin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CC(C)O[C@H]1CC[C@H](c2nnc3n2-c2ccc(Cl)cc2CN(Cc2ccccn2)C3)CC1
Reaction #324520
title compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
—
Reaction #358658
solid
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
Cc1nc(C#Cc2ccnc(Cl)c2)cn1Cc1ccccn1
Reaction #358659
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
Cc1nc(C#Cc2cccc(Cl)c2)cn1Cc1ccccn1
Reaction #358660
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
O=S(=O)(Nc1cc(Cl)ccc1SCc1ccccn1)c1cc2ccccc2o1
Reaction #419371
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cc1csc(Nc2ncc(SCc3ccccn3)cc2Oc2ccccc2)n1.Cl.Cl
Reaction #422264
N-(4-methylthiazol-2-yl)-3-phenoxy-5-(pyridin-2-ylmethylthio)pyridin-2-amine dihydrochloride
Ausbeute 60.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CCOC(=S)SCc1ccccn1
Reaction #436782
carbonodithioic acid, O-ethyl S-(2-pyridinylmethyl) ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
—
Reaction #488046
solid
Ausbeute 27.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
NC(=O)c1cccnc1
Reaction #491941
nicotinamide
Ausbeute 269.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
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