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1171586

CCCN(CCC)CC(=O)N1c2cc(F)c(F)cc2-n2c(nn(CCN3CCN(C)CC3)c2=O)-c2cccnc21
Reaction #209863
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc(F)cc1Nc1ccccn1
Reaction #330123
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(F)cc1Nc1ccccn1
Reaction #330124
title compound
Ausbeute 108.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)OC(C)(C)C)C(=O)Nc1ccc(F)cc1Nc1ccccn1
Reaction #330125
{(S)-1-[4-fluoro-2-(pyridin-2-ylamino)phenylcarbamoyl]ethyl}carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1ncnc2[nH]cnc12)C(=O)Nc1ccc(F)cc1Nc1ccccn1
Reaction #330126
title compound
Ausbeute 97.1%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(F)cc1Nc1ccc(F)cn1
Reaction #330177
title compound
Ausbeute 7.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(F)cc1Nc1ccc(F)cn1
Reaction #330178
title compound
Ausbeute 96.9%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)OC(C)(C)C)C(=O)Nc1ccc(F)cc1Nc1ccc(F)cn1
Reaction #330179
{(S)-1-[4-fluoro-2-(5-fluoropyridin-2-ylamino)phenylcarbamoyl]ethyl}carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(F)cc1Nc1ccccn1
Reaction #330186
title compound
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(F)cc1Nc1ccccn1
Reaction #330187
(5-fluoro-2-nitrophenyl)pyridin-2-yl-amine
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(F)cc1Nc1ccccn1
Reaction #330188
title compound
Ausbeute 101.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)OC(C)(C)C)c1nc2ccc(F)cc2n1-c1ccccn1
Reaction #330189
title compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)OC(C)(C)C)c1nc2ccc(F)cc2n1-c1ccccn1
Reaction #330190
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](COCc1ccccc1)c1nc2ccc(F)cc2n1-c1ccccn1
Reaction #330197
title compound
Ausbeute 53.4%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(F)c(Br)c1Nc1ccccn1
Reaction #330236
title compound
Ausbeute 60.5%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(F)c(Br)c1Nc1ccccn1
Reaction #330237
title compound
Ausbeute 75.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)OC(C)(C)C)c1nc2ccc(F)c(Br)c2n1-c1ccccn1
Reaction #330238
title compound
Ausbeute 56.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(F)ccc([N+](=O)[O-])c1Nc1ccccn1
Reaction #330241
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(F)ccc(N)c1Nc1ccccn1
Reaction #330242
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(F)ccc2nc([C@H](C)NC(=O)OC(C)(C)C)n(-c3ccccn3)c12
Reaction #330243
title compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
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