cyanomethyl trimethylphosphonium iodide

CCNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)[nH]c(=O)n3cccc43)CC2)cc1
Reaction #72591
N-ethyl-4-(4-((6-oxo-5,6-dihydropyrido[2,3-e]pyrrolo[1,2-c]pyrimidin-3-yl)methyl)piperazin-1-yl)benzamide
Rendimiento 59.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)[nH]c(=O)n3cccc43)CC2)cc1
Reaction #72593
N-methyl-4-(4-((6-oxo-5,6-dihydropyrido[2,3-e]pyrrolo[1,2-c]pyrimidin-3-yl)methyl)piperazin-1-yl)benzamide
Rendimiento 87.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(NC1CC1)c1ccc(N2CCN(Cc3cnc4c(c3)[nH]c(=O)n3cccc43)CC2)cc1
Reaction #72594
N-cyclopropyl-4-(4-((6-oxo-5,6-dihydropyrido[2,3-e]pyrrolo[1,2-c]pyrimidin-3-yl)methyl)piperazin-1-yl)benzamide
Rendimiento 69.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)[nH]c(=O)n3cccc43)CC2)c(Cl)c1
Reaction #72596
3-chloro-N-methyl-4-(4-((6-oxo-5,6-dihydropyrido[2,3-e]pyrrolo[1,2-c]pyrimidin-3-yl)methyl)piperazin-1-yl)benzamide
Rendimiento 74.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)[nH]c(=O)n3cccc43)CC2)c(Cl)c1
Reaction #72598
3-chloro-N-ethyl-4-(4-((6-oxo-5,6-dihydropyrido[2,3-e]pyrrolo[1,2-c]pyrimidin-3-yl)methyl)piperazin-1-yl)benzamide
Rendimiento 66.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)[nH]c(=O)n3cccc43)CC2)c(C)c1
Reaction #72603
N,3-dimethyl-4-(4-((6-oxo-5,6-dihydropyrido[2,3-e]pyrrolo[1,2-c]pyrimidin-3-yl)methyl)piperazin-1-yl)benzamide
Rendimiento 39.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)[nH]c(=O)n3cccc43)CC2)c(C)c1
Reaction #72606
N-ethyl-3-methyl-4-(4-((6-oxo-5,6-dihydropyrido[2,3-e]pyrrolo[1,2-c]pyrimidin-3-yl)methyl)piperazin-1-yl)benzamide
Rendimiento 30.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)[nH]c(=O)n3cccc43)CC2)c(F)c1
Reaction #72608
3-fluoro-N-methyl-4-(4-((6-oxo-5,6-dihydropyrido[2,3-e]pyrrolo[1,2-c]pyrimidin-3-yl)methyl)piperazin-1-yl)benzamide
Rendimiento 80.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)[nH]c(=O)n3cccc43)CC2)c(F)c1
Reaction #72610
N-ethyl-3-fluoro-4-(4-((6-oxo-5,6-dihydropyrido[2,3-e]pyrrolo[1,2-c]pyrimidin-3-yl)methyl)piperazin-1-yl)benzamide
Rendimiento 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C1Nc2cc(CN3CCN(c4ccc(Cl)cc4)CC3)cnc2N2CCC[C@@H]12
Reaction #156763
title compound
Rendimiento 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)[C@@H]3CCCN43)CC2)nc1
Reaction #156764
title compounds
Rendimiento 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)[C@@H]3CCCN43)CC2)cc1
Reaction #156774
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CNC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)[C@@H]3CCCN43)CC2)cc1
Reaction #156777
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(NC1CC1)c1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)[C@@H]3CCCN43)CC2)cc1
Reaction #156780
(S)—N-cyclopropyl-4-(4-((6-oxo-5,6,6a,7,8,9-hexahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-3-yl)methyl)piperazin-1-yl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#Cc1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)[C@@H]3CCCN43)CC2)c(F)c1
Reaction #156781
(S)-3-fluoro-4-(4-((6-oxo-5,6,6a,7,8,9-hexahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-3-yl)methyl)piperazin-1-yl)benzonitrile
Rendimiento 21.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1Nc2cc(CN3CCN(c4ccc(F)cc4F)CC3)cnc2N2CCC[C@@H]12
Reaction #156782
(S)-3-((4-(2,4-difluorophenyl)piperazin-1-yl)methyl)-6a,7,8,9-tetrahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-6(5H)-one
Rendimiento 23.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#Cc1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)[C@@H]3CCCN43)CC2)c(Cl)c1
Reaction #156785
(S)-3-chloro-4-(4-((6-oxo-5,6,6a,7,8,9-hexahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-3-yl)methyl)piperazin-1-yl)benzonitrile
Rendimiento 70.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1Nc2cc(CN3CCN(c4ccccc4)CC3)cnc2N2CCC[C@@H]12
Reaction #156786
title compound
Rendimiento 23.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1Nc2cc(CN3CC=C(c4ccc(Cl)cc4)CC3)cnc2N2CCCCC12
Reaction #156801
title compound
Rendimiento 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1Nc2cc(CN3CCN(c4ccc(Cl)cc4)CC3)cnc2N2CCCCC12
Reaction #156802
title compound
Rendimiento 41.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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