1,4-dibromobenzene

COC(=O)CN1CCN(c2ccc(Br)cc2)CC1
Reaction #571
Выход 0.0%750 AstraZeneca ELN dataset
CC1CN(c2ccc(Br)cc2)C1
Reaction #602
Выход 84.7%750 AstraZeneca ELN dataset
CCOC(=O)C1CCN(c2ccc(Br)cc2)CC1
Reaction #614
Выход 59.1%750 AstraZeneca ELN dataset
COC(=O)C1CCN(c2ccc(Br)cc2)C1
Reaction #615
Выход 29.1%750 AstraZeneca ELN dataset
COC(=O)C1CCN(c2ccc(Br)cc2)C1
Reaction #616
Выход 31.6%750 AstraZeneca ELN dataset
OC1(c2ccc(Br)cc2)CCC1
Reaction #9329
3-1
Выход 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CN1C[C@H]2CCN(c3ccc(Br)cc3)[C@H]2C1
Reaction #41230
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1C[C@H]2CCN(c3ccc(Br)cc3)[C@H]2C1
Reaction #41247
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
OC1(c2ccc(Br)cc2)CCC1
Reaction #48042
1-(4-bromophenyl)-cyclobutanol
Выход 34.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Brc1ccc(-c2ccccn2)cc1
Reaction #51197
title product
Выход 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C(c1ccc(Br)cc1)c1ccccn1
Reaction #64173
4-[2-pyridylcarbonyl]bromobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Brc1ccc(-n2c3ccccc3c3ccccc32)cc1
Reaction #70062
9-(4-bromophenyl)-9H-carbazole
Выход 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(NCCCc1ccc(Br)cc1)OCc1ccccc1
Reaction #76650
N-[3-(4-bromophenyl)propyl](phenylmethoxy)carboxamide
Выход 54.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
C[Si](C)(C)c1ccc(Br)cc1
Reaction #92899
p-bromotrimethylsilylbenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
COC(=O)NC(C(=O)N1CCCC1c1ncc(-c2ccc(-c3ccc(Br)cc3)cc2)[nH]1)C(C)C
Reaction #158895
(1-{2-[5-(4′-bromo-biphenyl-4-yl)-1H-imidazol-2-yl]-pyrrolidine-1-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester
Выход 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)NC(C(=O)N1CCCC1c1ncc(C#Cc2ccc(Br)cc2)[nH]1)C(C)C
Reaction #159028
(1-{2-[5-(4-Bromo-phenylethynyl)-1H-imidazol-2-yl]-pyrrolidine-1-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester
Выход 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)Nc1ccc(-c2ccc(Br)cc2)cc1
Reaction #159035
(4′-Bromo-biphenyl-4-yl)-carbamic acid tert-butyl ester
Выход 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)NC(C(=O)N1CCCC1c1ncc(-c2ccc(-c3ccc(Br)cc3)cc2)[nH]1)C(C)C
Reaction #166850
(1-{2-[5-(4′-bromo-biphenyl-4-yl)-1H-imidazol-2-yl]-pyrrolidine-1-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester
Выход 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)NC(C(=O)N1CCCC1c1ncc(C#Cc2ccc(Br)cc2)[nH]1)C(C)C
Reaction #166978
(1-{2-[5-(4-Bromo-phenylethynyl)-1H-imidazol-2-yl]-pyrrolidine-1-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester
Выход 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)Nc1ccc(-c2ccc(Br)cc2)cc1
Reaction #166985
(4′-Bromo-biphenyl-4-yl)-carbamic acid tert-butyl ester
Выход 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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