Involved in 645 reactions

915

Brc1cccc(NC2CCOCC2)n1
Reaction #823
Yield 0.0%750 AstraZeneca ELN dataset
CS(=O)(=O)c1ccc(-c2cc(C(F)(F)F)nc(NC3CCOCC3)n2)cc1
Reaction #6792
title compound
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1cc2cnc(NC3CCOCC3)nc2s1
Reaction #9867
title compound
Yield 72.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Clc1ncc(Br)c(NC2CCOCC2)n1
Reaction #66495
desired product
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1nc(NCc2ccccn2)nc(NC2CCOCC2)c1C
Reaction #91402
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=[N+]([O-])c1cc(C(F)(F)F)ccc1NC1CCOCC1
Reaction #161332
title compound
Yield 90.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(O)c1ccc(NC2CCOCC2)c([N+](=O)[O-])c1
Reaction #161339
title compound
Yield 101.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=[N+]([O-])c1cc(Br)ccc1C1CCOCC1
Reaction #161364
title compound
Yield 91.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1cc(-c2nc3cc(Cl)ccc3o2)ccc1NC1CCOCC1
Reaction #161465
title compound
Yield 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=[N+]([O-])c1cc(-c2nc3ccccc3o2)c(Cl)cc1NC1CCOCC1
Reaction #161476
title compound
Yield 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(NC1CCOCC1)C(O)c1ccc(-c2noc(-c3onc(-c4ccccc4)c3C(F)(F)F)n2)cc1
Reaction #164332
(R/S)-2-hydroxy-2-(4-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)-N-(tetrahydro-2H-pyran-4-yl)acetamide
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)c1cn(C2CCOCC2)c(=N)s1
Reaction #165714
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Clc1ncc(Br)c(NC2CCOCC2)n1
Reaction #166292
(5-bromo-2-chloro-pyrimidin-4-yl)-(tetrahydro-pyran-4-yl)-amine
Yield 105.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)S(=O)(=O)c1ccc(-c2cnc(N)c(-c3cc(-c4ccc(CNC5CCOCC5)cc4)no3)n2)cc1
Reaction #168560
5-(4-isopropylsulfonylphenyl)-3-[3-[4-[(tetrahydropyran-4-ylamino)methyl]phenyl]isoxazol-5-yl]pyrazin-2-amine
Yield 87.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)NC2CCOCC2)cn1
Reaction #170322
title compound
Yield 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)NC2CCCN(CC(=O)NC3CCOCC3)C2)cn1
Reaction #170335
title compound
Yield 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1onc(-c2ccccc2)c1COc1cc(C(=O)NC2CCOCC2)ccn1
Reaction #170349
title compound
Yield 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1onc(-c2ccccc2)c1COc1cc(C(F)(F)F)c(C(=O)NC2CCOCC2)cn1
Reaction #170353
title compound
Yield 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1onc(-c2ccccc2F)c1COc1ccc(C(=O)NC2CCOCC2)cn1
Reaction #170381
title compound
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1onc(-c2cccc(F)c2)c1COc1ccc(C(=O)NC2CCOCC2)cn1
Reaction #170392
title compound
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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