Teilstruktursuche

Cn1cccn1

CN1CC(CCn2cccn2)Oc2ncccc2C1=O
Reaction #4935
2,3-Dihydro-4-methyl-2-[2-(1H-pyrazol-1-yl)ethyl]pyrido[3,2-f][1,4]oxazepin-5(4H)-one
DOI: 10.6084/m9.figshare.5104873.v1
NSOOc1ccc(-n2nc(C(N)=O)c3c2-c2cc(N)ccc2CC3)cc1
Reaction #51257
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NSOOc1ccc(-n2nc(C(N)=O)c3ccc4ccc(N)cc4c32)cc1
Reaction #51258
title compound
Ausbeute 90.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc2c(c1)-c1c(c(C(N)=O)nn1-c1ccc(OOSN)cc1)CC2
Reaction #51259
8-(acetylamino)-1-{4-[(aminothio)peroxy]phenyl}-4,5-dihydro-1H-benzo[g]indazole-3-carboxamide
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OC/C=C/Cl)nc(Oc2cc(C(F)(F)F)nn2C)c1
Reaction #51596
title compound
Ausbeute 52.3%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(/C=C/C(=O)O)cn1
Reaction #58960
(2E)-3-(1-methyl-1H-pyrazol-4-yl)acrylic acid
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCSCCC(F)(F)F)Nc1cn(-c2cccnc2)nc1Cl
Reaction #84020
solid
Ausbeute 53.3%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C(=O)CCSCCC(F)(F)F)c1cn(-c2cccnc2)nc1Cl
Reaction #84021
oil
Ausbeute 66.4%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C(=O)CCSCCC(F)(F)F)c1cn(-c2cccnc2)nc1Cl
Reaction #84022
N-(3-chloro-1-(pyridin-3-yl)-1H-pyrazol-4-yl)-N-ethyl-3-((3,3,3-trifluoropropyl)thio)propanamide
DOI: 10.6084/m9.figshare.5104873.v1
CCN(C(=O)CCSCCC(F)(F)F)c1cn(-c2cccnc2)nc1Cl
Reaction #85380
N-(3-Chloro-1-(pyridin-3-yl)-1H-pyrazol-4-yl)-N-ethyl-3-((3,3,3-trifluoropropyl)thio)propanamide
DOI: 10.6084/m9.figshare.5104873.v1
CCN(C(=O)CCSCCC(F)(F)F)c1cn(-c2cccnc2)nc1Cl
Reaction #85381
solid
Ausbeute 86.5%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C(=O)CCSCCC(F)(F)F)c1cn(-c2cccnc2)nc1Cl
Reaction #85382
desired product
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCSCCC(F)(F)F)Nc1cn(-c2cccnc2)nc1Cl
Reaction #91104
solid
Ausbeute 53.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1ncc(CC(=O)O)c1C(F)(F)F
Reaction #169410
title compound
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c(CNC(=O)c2cc(Br)cc3c2cnn3C(C)C)c(=O)[nH]1
Reaction #172599
title compound
Ausbeute 87.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c(CNC(=O)c2cc(-c3ccc(N4CCNCC4)nc3)cc3c2cnn3C(C)C)c(=O)[nH]1
Reaction #172606
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c(CNC(=O)c2cc(-c3cnn(C)c3)cc3c2cnn3C(C)C)c(=O)[nH]1
Reaction #172609
title compound
Ausbeute 77.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c(CNC(=O)c2cc(-c3ccc(N(C)C)nc3)cc3c2cnn3C(C)C)c(=O)[nH]1
Reaction #172621
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c(CNC(=O)c2cc(-c3ccc(C(F)(F)F)nc3)cc3c2cnn3C(C)C)c(=O)[nH]1
Reaction #172622
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c(CNC(=O)c2cc(-c3cccc(CN(C)C)c3)cc3c2cnn3C(C)C)c(=O)[nH]1
Reaction #172623
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter