Recherche de Sous-structure

46

Cc1ncc([N+](=O)[O-])cc1Nc1nccc(-c2cccnc2)n1
Reaction #732
Rendement 18.9%
Cc1ncc([N+](=O)[O-])cc1Nc1nccc(-c2cccnc2)n1
Reaction #733
Rendement 21.2%
Nc1cccc2c(O)ncc(Br)c12
Reaction #10686
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(O)c2cccc(N)c12
Reaction #10687
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cccc2cncc(Br)c12
Reaction #10690
title compound
Rendement 55.9%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc[nH]c2cc(Br)cnc12
Reaction #68648
7-bromo-1,5-naphthyridin-4(1H)-one
Rendement 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccnc2cc(Br)cnc12
Reaction #68649
3-bromo-8-chloro-1,5-naphthyridine
Rendement 14.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2ncc([N+](=O)[O-])cc2Br)c1
Reaction #70269
3-bromo-2-(3-methoxyphenyl)-5-nitropyridine
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc(Br)c(Br)c1
Reaction #70272
expected product
Rendement 73.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2ncc([N+](=O)[O-])cc2Br)c1
Reaction #70273
3-Bromo-2-(3-methoxyphenyl)-5-nitropyridine
Rendement 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)N1CCC(CC(=O)N2CCN(C3c4ccc(Cl)cc4CCc4cc(Br)cnc43)CC2)CC1
Reaction #75628
title compound
Rendement 84.8%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(OC2CCOCC2)nc1
Reaction #85825
white solid
Rendement 79.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(Nc2nc3c(Br)cccn3n2)cc1
Reaction #86047
methyl 4-(8-bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamino)benzoate
Rendement 68.7%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOCn1c2cnc(C#N)cc2c2cccnc21
Reaction #88525
title compound
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(C)(COc2c(Br)cnc3[nH]c4cnc(C#N)cc4c23)CC1
Reaction #88546
title compound
Rendement 38.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)n1c2cncc(O)c2c2cc(Br)cnc21
Reaction #88613
title compound
Rendement 17.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2cncc3c2c2cc(Br)cnc2n3C(=O)OCc2ccccc2)CC1
Reaction #88614
title compound
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Br)c(C(=O)N2CCC[C@@H](C)[C@H]2CN2C(=O)c3ccccc3C2=O)n1
Reaction #89389
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ncccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CN2C(=O)c3ccccc3C2=O)n1
Reaction #89390
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]1(N2C(=O)c3ccc(CNC(=O)c4ccc(Br)cn4)cc3C2=O)CCC(=O)NC1=O
Reaction #91686
5-bromo-N-[[2-[(3S)-3-methyl-2,6-dioxopiperidin-3-yl]-1,3-dioxoisoindolin-5-yl]methyl]picolinamide
Rendement 57.0%DOI: 10.6084/m9.figshare.5104873.v1
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