cyclopropanamine

CCOC(=O)C(=CNC1CC1)C(=O)c1c(F)cc(F)c(F)c1C
Reaction #1373
ethyl 2-(2-methyl-3,4,6-trifluorobenzoyl)-3-cyclopropylaminoacrylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(NC1CC1)c1ccccc1SSc1ccccc1C(=O)NC1CC1
Reaction #3832
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)C(=CNC1CC1)C(=O)c1cc(F)c(-n2cccc2)cc1F
Reaction #4666
crystals
Ausbeute 36.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)c1nc(C(=O)NC2CC2)co1
Reaction #5427
2-isopropyl-oxazole-4-carboxylic acid-cyclopropylamide
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(NC1CC1)c1ccc(F)c(O)c1
Reaction #6966
3-hydroxy-4-fluoro-N-cyclopropylbenzamide
Ausbeute 61.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=[N+]([O-])c1cc(S(=O)(=O)NC2CC2)ccc1F
Reaction #6978
N-cyclopropyl-4-fluoro-3-nitrobenzenesulfonamide
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)/C(NC(C)=O)=C(\C)NC1CC1
Reaction #8988
(Z)-2-Acetylamino-3-cyclopropylamino-but-2-enoic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1cc(F)c(N2CC[C@H](NC(=O)OC(C)(C)C)C2)c(F)c1NC1CC1
Reaction #10384
title compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1c(F)cc(N2CC[C@H](NC(=O)OC(C)(C)C)C2)c(F)c1NC1CC1
Reaction #10385
title compound
Ausbeute 81.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1cc(F)c(N2CC[C@H](NC(=O)OC(C)(C)C)C2)c(Cl)c1NC1CC1
Reaction #10386
title compound
Ausbeute 43.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)N[C@H]1CCN(c2c(F)c(F)c(C(=O)OCc3ccccc3)c(NC3CC3)c2F)C1
Reaction #10387
title compound
Ausbeute 86.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1ccc(N2CCC(NC(=O)OC(C)(C)C)C2)c(F)c1NC1CC1
Reaction #10390
title compound
Ausbeute 76.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1cc(Cl)c(N2CCC(NC(=O)OC(C)(C)C)C2)c(F)c1NC1CC1
Reaction #10391
title compound
Ausbeute 48.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)c1cc(F)c(F)c(Cl)c1NC1CC1
Reaction #10398
title compound
Ausbeute 63.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(NC(=O)c1cc(F)c(Cl)nc1Cl)NC1CC1
Reaction #10425
title compound
Ausbeute 98.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1cc(F)c(SC)nc1NC1CC1
Reaction #10438
title compound
Ausbeute 69.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N[C@@H](CC(=O)N1CCC[C@H]1C(=O)NCc1cc(Cl)ccc1OCC(=O)NC1CC1)Cc1ccccc1
Reaction #11515
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(NC1CC1)c1ccc(Br)cc1F
Reaction #44391
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
NS(=O)(=O)c1cc(Cl)c(Cl)cc1NC1CC1
Reaction #46113
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
NS(=O)(=O)c1cc([N+](=O)[O-])ccc1NC1CC1
Reaction #46116
2-cyclopropylamino-5-nitrobenzenesulphonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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