Teilstruktursuche

548251

C[C@@H](Cc1c(F)c(F)cc(F)c1F)N=[N+]=[N-]
Reaction #156518
(2S)-3-(2-Azidopropyl)-1,2,4,5-tetrafluorobenzene
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Cc1c(F)c(F)cc(F)c1F)Nc1cc[nH]c(=O)c1-c1nc2cc3c(cc2[nH]1)C(=O)N(C1CCN(C)CC1)C3=O
Reaction #156522
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Cc1c(F)c(F)cc(F)c1F)Nc1cc[nH]c(=O)c1-c1nc2cc3c(cc2[nH]1)C(=O)N(C1CCN(C)CC1)C3
Reaction #156523
title compound
Ausbeute 13.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Cc1c(F)c(F)cc(F)c1F)Nc1cc[nH]c(=O)c1-c1nc2cc3c(cc2[nH]1)C(=O)N(c1cccnc1)C3=O
Reaction #156528
(S)-2-(2-oxo-4-((1-(2,3,5,6-tetrafluorophenyl)propan-2-yl)amino)-1,2-dihydropyridin-3-yl)-6-(pyridin-3-yl)imidazo[4,5-f]isoindole-5,7(1H,6H)-dione
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Cc1c(F)c(F)cc(F)c1F)Nc1cc[nH]c(=O)c1-c1nc2cc3c(cc2[nH]1)C(=O)N(c1ccc(F)nc1)C3=O
Reaction #156530
(S)-6-(6-Fluoropyridin-3-yl)-2-(2-oxo-4-((1-(2,3,5,6-tetrafluorophenyl)propan-2-yl)amino)-1,2-dihydropyridin-3-yl)imidazo[4,5-f]isoindole-5,7(1H,6H)-dione
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c2c(cc3[nH]c(-c4c(NC(C)Cc5c(F)c(F)cc(F)c5F)cc[nH]c4=O)nc13)C(=O)N(C1CCN(C)CC1)C2=O
Reaction #156534
designed compound
Ausbeute 78.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c2c(cc3[nH]c(-c4c(NC(C)Cc5c(F)c(F)cc(F)c5F)cc[nH]c4=O)nc13)CN(C1CCN(C)CC1)C2=O
Reaction #156535
designed compound
Ausbeute 36.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c2c(cc3[nH]c(-c4c(NC(C)Cc5c(F)c(F)cc(F)c5F)cc[nH]c4=O)nc13)C(=O)N(C1CCN(C)CC1)C2
Reaction #156536
designed compound
Ausbeute 11.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c2c(cc3[nH]c(-c4c(NC(C)Cc5c(F)c(F)cc(F)c5F)cc[nH]c4=O)nc13)C(=O)N(CCN(C)C)C2=O
Reaction #156541
designed compound
Ausbeute 42.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c2c(cc3[nH]c(-c4c(NC(C)Cc5c(F)c(F)cc(F)c5F)cc[nH]c4=O)nc13)CN(CCN(C)C)C2=O
Reaction #156542
designed compound
Ausbeute 81.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c2c(cc3[nH]c(-c4c(NC(C)Cc5c(F)c(F)cc(F)c5F)cc[nH]c4=O)nc13)C(=O)N(CCN(C)C)C2
Reaction #156543
designed compound
Ausbeute 12.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(Cc1c(F)c(F)cc(F)c1F)Nc1cc[nH]c(=O)c1-c1nc2cc3c(cc2[nH]1)C(=O)N(C)C3=O
Reaction #156561
2-(4-(1-(2,3,5,6-Tetrafluorophenyl)propan-2-ylamino)-2-oxo-1,2-dihydropyridin-3-yl)-6-methylimidazo[4,5-f]isoindole-5,7(1H,6H)-dione
Ausbeute 75.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(Cc1c(F)c(F)cc(F)c1F)Nc1cc[nH]c(=O)c1-c1nc2cc3c(cc2[nH]1)CN(C)C3=O
Reaction #156562
6-Methyl-2-(2-oxo-4-(1-(2,3,5,6-tetrafluorophenyl)propan-2-ylamino)-1,2-dihydropyridin-3-yl)-6,7-dihydroimidazo[4,5-f]isoindole-5(1H)-one
Ausbeute 62.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Cc1c(F)c(F)cc(F)c1F)N=[N+]=[N-]
Reaction #1007644
(2S)-3-(2-Azidopropyl)-1,2,4,5-tetrafluorobenzene
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Cc1c(F)c(F)cc(F)c1F)Nc1cc[nH]c(=O)c1-c1nc2cc3c(cc2[nH]1)C(=O)N(C1CCN(C)CC1)C3=O
Reaction #1007648
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Cc1c(F)c(F)cc(F)c1F)Nc1cc[nH]c(=O)c1-c1nc2cc3c(cc2[nH]1)C(=O)N(C1CCN(C)CC1)C3
Reaction #1007649
title compound
Ausbeute 13.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Cc1c(F)c(F)cc(F)c1F)Nc1cc[nH]c(=O)c1-c1nc2cc3c(cc2[nH]1)C(=O)N(c1cccnc1)C3=O
Reaction #1007654
(S)-2-(2-oxo-4-((1-(2,3,5,6-tetrafluorophenyl)propan-2-yl)amino)-1,2-dihydropyridin-3-yl)-6-(pyridin-3-yl)imidazo[4,5-f]isoindole-5,7(1H,6H)-dione
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Cc1c(F)c(F)cc(F)c1F)Nc1cc[nH]c(=O)c1-c1nc2cc3c(cc2[nH]1)C(O)N(c1cccnc1)C3=O
Reaction #1007655
7-Hydroxy-2-(2-oxo-4-(((S)-1-(2,3,5,6-tetrafluorophenyl)propan-2-yl)amino)-1,2-dihydropyridin-3-yl)-6-(pyridin-3-yl)-6,7-dihydroimidazo[4,5-f]isoindol-5(1H)-one
Ausbeute 32.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Cc1c(F)c(F)cc(F)c1F)Nc1cc[nH]c(=O)c1-c1nc2cc3c(cc2[nH]1)C(=O)N(c1ccc(F)nc1)C3=O
Reaction #1007657
(S)-6-(6-Fluoropyridin-3-yl)-2-(2-oxo-4-((1-(2,3,5,6-tetrafluorophenyl)propan-2-yl)amino)-1,2-dihydropyridin-3-yl)imidazo[4,5-f]isoindole-5,7(1H,6H)-dione
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c2c(cc3[nH]c(-c4c(NC(C)Cc5c(F)c(F)cc(F)c5F)cc[nH]c4=O)nc13)C(=O)N(C1CCN(C)CC1)C2=O
Reaction #1007661
designed compound
Ausbeute 78.5%DOI: 10.6084/m9.figshare.5104873.v1
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