5-bromo-2-chloro-pyrimidine

COc1cccc(Oc2c(NS(=O)(=O)c3ccc(C(C)(C)C)cc3)ncnc2OCCOc2ncc(Br)cn2)c1
Reaction #2366
N-[-6-{2-(5-bromopyrimidin-2-yloxy)ethoxy}-5-(3-methoxyphenoxy)pyrimidin-4-yl]-4-tert-butylbenzenesulfonamide
Yield 84.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCc1nc(NS(=O)(=O)c2ccc(C(C)(C)C)cc2)c(-c2ccc(C)cc2)c(OCCOc2ncc(Br)cn2)n1
Reaction #2387
4-tert-butyl-N-[6-{2-(5-bromopyrimidin-2-yloxy)ethoxy}-5-(4-methylphenyl)-2-n-propylpyrimidin-4-yl]benzenesulfonamide
Yield 91.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(-c2c(NS(=O)(=O)c3ccc(C(C)(C)COc4ncc(Br)cn4)cc3)ncnc2OCCOc2ncc(Br)cn2)cc1
Reaction #2395
4-[2-(5-bromopyrimidin-2-yloxy)-1,1-dimethylethyl]-N-{6-[2-(5-bromopyrimidin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamide
Yield 33.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(-c2c(NS(=O)(=O)c3ccc(C(C)(C)C)cc3)ncnc2OCCOc2ncc(Oc3ncc(Br)cn3)cn2)cc1
Reaction #2396
4-tert-butyl-N-{6-[2-(5-(5-bromopyrimidin-2-yloxy)pyrimidin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamide
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(-c2c(N)ncnc2OCCOc2ncc(Br)cn2)cc1
Reaction #2402
6-[2-(5-bromopyrimidin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-amine
Yield 91.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Clc1ncc(-c2ccco2)cn1
Reaction #2416
2-chloro-5-(2-furyl)pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Clc1ncc(-c2ccsc2)cn1
Reaction #2417
2-chloro-5-(3-thienyl)pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1ccc(Oc2ncc(Br)cn2)c(Cl)c1
Reaction #4608
4-(5-bromo-2-pyrimidinyloxy)-3-chloroaniline
Yield 62.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COc1ccccc1Oc1c(NS(=O)(=O)Nc2ccc(C(C)C)cc2)nc(-c2ccncc2)nc1OCCOc1ncc(Br)cn1
Reaction #10348
4-i-propyl-phenyl sulfamic acid-[6-[2-(5-bromo-pyrimidin-2-yloxy)-ethoxy]-5-(o-methoxy-phenoxy)-2-(4-pyridyl)-pyrimidin-4-yl]-amide
Yield 71.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc(NS(=O)(=O)Nc2ncnc(OCCOc3ncc(Br)cn3)c2-c2ccc(C)cc2)cc1
Reaction #10353
4-methyl-phenyl sulfamic acid-[6-[2-(5-bromo-pyrimidin-2-yloxy)-ethoxy]-5-(p-tolyl)-4-pyrimidinyl]-amide
Yield 52.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(Cl)c(Oc2c(NS(=O)(=O)NCc3ccccc3)ncnc2OCCOc2ncc(Br)cn2)c1
Reaction #10362
Benzylsulfamic acid [6-[2-(5-bromo-pyrimidin-2-yloxy)-ethoxy]-5-(2-chloro-5-methoxy-phenoxy)-pyrimidin-4-yl]-amide
Yield 48.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(COc1ncc(Br)cn1)OCC
Reaction #43341
title compound
Yield 94.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)O.O=C(O)N1CCCC[C@H]1CNc1ncc(Br)cn1
Reaction #46379
title compound
Yield 141.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)O.O=C(O)N1CCC[C@H]1CNc1ncc(Br)cn1
Reaction #46380
title compound
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #49147
solid
Yield 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CCN(c2ncc(Br)cn2)CC1
Reaction #57279
title compound
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CN1CCN(c2ncc(Br)cn2)CC1
Reaction #57280
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Brc1cnc(OC2CCC2)nc1
Reaction #68839
5-Bromo-2-cyclobutoxy-pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Brc1cnc(NC2CCC2)nc1
Reaction #68840
5-Bromo-N-cyclobutylpyrimidin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCC(C)Nc1ncc(Br)cn1
Reaction #68841
5-Bromo-N-sec-butylpyrimidin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Page 1Next