Recherche de Sous-structure

484

Clc1ccnc(Nc2ncco2)c1
Reaction #415
Rendement 0.5%
Clc1ccnc(Nc2ncco2)c1
Reaction #416
Rendement 7.7%
CCOC(=O)c1c(Cl)c(C)c(=O)n(C)c1Br
Reaction #44227
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)c(C)c(=O)n(C)c1C#C[Si](C)(C)C
Reaction #44228
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccnc(Br)c1Cl
Reaction #48917
2-bromo-3,4-dichloropyridine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2cc(Br)ncc2[N+](=O)[O-])cc1
Reaction #68930
title compound
Rendement 77.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(CNc2cc(Br)ncc2[N+](=O)[O-])CC1
Reaction #232180
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1c(Cl)cc(Br)nc1Br
Reaction #296866
DOI: 10.1039/C8SC04228D
CCOc1ccc2c(Cl)cc(Br)nc2c1
Reaction #299408
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(CNc2cc(Br)ncc2[N+](=O)[O-])CC1
Reaction #471810
tert-butyl 4-((2-bromo-5-nitropyridin-4-ylamino)methyl)piperidine-1-carboxylate
Rendement 98.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(COc2cc(Br)ncc2[N+](=O)[O-])CC1
Reaction #471832
tert-butyl 4-((2-bromo-5-nitropyridin-4-yloxy)methyl)piperidine-1-carboxylate
Rendement 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC(CNc2cc(Br)ncc2[N+](=O)[O-])C1
Reaction #471837
tert-butyl 3-((2-bromo-5-nitropyridin-4-ylamino)methyl)piperidine-1-carboxylate
Rendement 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1c(Cl)ccnc1Br
Reaction #494795
103a
Rendement 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(F)c2c(=O)n(-c3nccc(Cl)c3C=O)ncc2c1
Reaction #494796
103b
Rendement 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)c(C)c(=O)n(C)c1Br
Reaction #509073
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)c(C)c(=O)n(C)c1C#C[Si](C)(C)C
Reaction #509074
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)c(C)c(=O)n(C)c1Br
Reaction #509981
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)c(C)c(=O)n(C)c1C#C[Si](C)(C)C
Reaction #509982
desired product
DOI: 10.6084/m9.figshare.5104873.v1
OCc1c(Cl)ccnc1Br
Reaction #607504
(2-bromo-4-chloropyridin-3-yl)methanol
Rendement 99.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OCc1c(Cl)ccnc1Br
Reaction #607505
2-bromo-3-(((tert-butyldimethylsilyl)oxy)methyl)-4-chloropyridine
Rendement 99.0%DOI: 10.6084/m9.figshare.5104873.v1
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