diethylmethylamine

COCCNS(=O)(=O)c1ccc(Nc2nccc(-c3cnc(C=O)n3C(C)C)n2)cc1
Reaction #60626
title compound
Ausbeute 24.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC[NH+](C)CC.O=S(=O)([O-])C(F)(F)F
Reaction #70115
diethylmethylammonium trifluoromethanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)c1ncc(-c2ccnc(Nc3ccc(S(=O)(=O)NC4CCC4)cc3)n2)n1C
Reaction #406910
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(NC1=N[C@@]2(c3cccs3)CN(C(=O)OCc3ccccc3)C[C@H]2CS1)c1ccccc1
Reaction #425312
title compound
Ausbeute 46.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
O=C(NC1=N[C@@]2(c3cccs3)CN(C(=O)OCc3ccccc3)C[C@H]2CS1)c1ccccc1
Reaction #557435
title compound
Ausbeute 46.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CC[N+](C)(CC)COC.[Cl-]
Reaction #730368
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
CC[NH+](C)CC.O=S(=O)([O-])C(F)(F)F
Reaction #742269
Diethylmethylammonium Trifluoromethanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
CCN(C(C)C)C(C)C
Reaction #980107
diisopropylethylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_06
CCn1c(-c2ccnc(Nc3ccc(S(=O)(=O)NCCOCCO)cc3)n2)cnc1C
Reaction #1151497
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_11
CCOCCNS(=O)(=O)c1ccc(Nc2nccc(-c3cnc(C)n3CC)n2)cc1
Reaction #1650943
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
COCCNS(=O)(=O)c1ccc(Nc2nccc(-c3cnc(C=O)n3C(C)C)n2)cc1
Reaction #1651647
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
O=C(NC1=N[C@@]2(c3cccs3)CN(C(=O)OCc3ccccc3)C[C@H]2CS1)c1ccccc1
Reaction #1706214
title compound
Ausbeute 46.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
CCN(C)CC
Reaction #1764048
diethylmethylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_08
CC(C)c1ncc(-c2ccnc(Nc3ccc(S(=O)(=O)NC4CCC4)cc3)n2)n1C
Reaction #2204925
title compound
Ausbeute 65.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_10
CCOCCNS(=O)(=O)c1ccc(Nc2nccc(-c3cnc(C)n3CC)n2)cc1
Reaction #2462450
title compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12