An 1567 Reaktionen beteiligt

580

CNc1cncc(C(F)(F)F)c1
Reaction #278
Ausbeute 0.0%750 AstraZeneca ELN dataset
CNC(=O)c1ccc(C)c(I)c1
Reaction #3063
N-methyl-(3-iodo-4-methylphenyl)carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)N1CCC(CN)CC1
Reaction #10622
title compound
Ausbeute 93.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CNC(=O)c1ccc(Br)cc1F
Reaction #44395
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CNC(=O)c1nc2c(C#N)c(C)c(-c3ccccc3)c(F)c2o1
Reaction #45648
compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCN(CC)c1nc2c(C#N)c(C)c(-c3ccccc3)c(F)c2o1
Reaction #45681
compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CNCC(O)c1cccc(OCOC)c1
Reaction #48901
title product
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CNCc1ccc2c(c1)cc(-c1cc(OC)c(O)c3c1C(=O)NC3)n2C(=O)OC(C)(C)C
Reaction #49562
4-hydroxy-5-methoxy-7-[1-(tert-butoxycarbonyl)-5-(methylaminomethyl)indol-2-yl]isoindolinone
Ausbeute 31.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCC12CCC(C(=O)NC)(CC1)CC2
Reaction #51113
N-methyl-4-pentylbicyclo[2.2.2]octane-1-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CNC(=O)c1ccc(N/C(=C2\C(=O)Nc3ccccc32)c2ccccc2)cc1
Reaction #53027
(Z)-3-[1-(4-methylaminocarbonyl-phenylamino)-1-phenyl-me-thylidene]-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CNC(=O)c1cccc(N/C(=C2\C(=O)Nc3ccccc32)c2ccccc2)c1
Reaction #53029
(Z)-3-[1-(3-methylaminocarbonyl-phenylamino)-1-phenyl-methylidene]-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CNC(=O)C(SCCCl)SCCCl
Reaction #64074
4c
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC=C(C(=O)NC)c1ccccc1COC
Reaction #64884
title compound
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CNS(=O)(=O)CCCCl
Reaction #65154
N-methyl-3-chloropropylsulfonamide
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CNC(=O)C1CNCCc2c1[nH]c1ccccc21
Reaction #66247
title compound
Ausbeute 65.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CNC(=O)c1cc(OC)cc2c1ccc(=O)n2CCN1CCC(N(Cc2ccc3c(c2)OCCO3)C(=O)OC(C)(C)C)CC1
Reaction #68142
tert-butyl (2,3-dihydro-1,4-benzodioxin-6-ylmethyl)(1-(2-(7-methoxy-5-((methylamino)carbonyl)-2-oxoquinolin-1(2H)-yl)ethyl)piperidin-4-yl)carbamate
Ausbeute 84.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CNC(=O)COc1cccc2c1ccc(=O)n2CCN1CCC(N(Cc2ccc3c(c2)OCCO3)C(=O)OC(C)(C)C)CC1
Reaction #68205
tert-butyl (2,3-dihydro-1,4-benzodioxin-6-ylmethyl)(1-(2-(5-((methylamino)carbonylmethyloxy)-2-oxoquinolin-1(2H)-yl)ethyl)piperidin-4-yl)carbamate
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
—
Reaction #68819
solid
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1sc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OC)C2)nc1C(=O)NC
Reaction #71780
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1sc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OCC)C2)nc1C(=O)NC
Reaction #71806
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
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