Busqueda de Subestructura

778078

O=C(OCCO)c1cnc(Cl)c(Br)c1
Reaction #299587
DOI: 10.1039/C8SC04228D
O=C(Cl)c1cc(Br)cnc1Cl
Reaction #341137
5-bromo-2-chloropyridine-3-carbonyl chloride
Rendimiento 99.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc(Cl)c1Cl)c1cc(Br)cnc1Cl
Reaction #341138
5-bromo-2-chloro-N-(2,3-dichlorophenyl)pyridine-3-carboxamide
Rendimiento 79.1%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(Cl)c1cncc(Br)c1
Reaction #556507
5-bromo-nicotinic acid chloride hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)c2cncc(Br)c2)cc2oc(=O)[nH]c12
Reaction #556508
6-(5-bromo-pyridin-3-carbonyl)-4-methyl-3H-benzoxazol-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1cc(Br)cnc1Cl
Reaction #907389
DOI: 10.1039/C8SC04228D
O=C(Cl)c1cc(Br)cnc1Cl
Reaction #1035487
DOI: 10.1039/C8SC04228D
CON(C)C(=O)c1cc(Br)cnc1Cl
Reaction #1311888
DOI: 10.1039/C8SC04228D
O=C(OCCO)c1cnc(Cl)c(Br)c1
Reaction #1562934
title compound
Rendimiento 77.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1cc(Br)cnc1Cl
Reaction #1605691
5-bromo-2-chloropyridine-3-carbonyl chloride
Rendimiento 99.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc(Cl)c1Cl)c1cc(Br)cnc1Cl
Reaction #1605692
5-bromo-2-chloro-N-(2,3-dichlorophenyl)pyridine-3-carboxamide
Rendimiento 79.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc(Cl)c1Cl)c1cc(Br)cnc1Cl
Reaction #1650205
DOI: 10.1039/C8SC04228D
O=C(OCCO)c1cnc(Cl)c(Br)c1
Reaction #2005523
title compound
Rendimiento 77.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc(-n2c(=O)c(Cc3cccnc3)nc3cccnc32)c1)c1cncc(Br)c1
Reaction #2040600
4-[3-[(5-bromo-3-pyridyl)carbonylamino]phenyl]-2-(3-pyridylmethyl)-3-oxo-3,4-dihydropyrido[2,3-b]pyrazine
Rendimiento 54.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1cc(Br)cnc1Cl
Reaction #2158061
5-bromo-2-chloronicotinoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)c1cc(Br)cnc1Cl
Reaction #2158062
5-bromo-2-chloro-N-methoxy-N-methylnicotinamide
Rendimiento 71.4%DOI: 10.6084/m9.figshare.5104873.v1
Reaction #2316484
solid
Rendimiento 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNc1nc(Cl)ccc1NC(=O)c1cc(Br)cnc1Cl
Reaction #2316488
title compound
Rendimiento 75.1%DOI: 10.6084/m9.figshare.5104873.v1
CCNc1nc(F)ccc1NC(=O)c1cc(Br)cnc1Cl
Reaction #2316497
title compound
Rendimiento 99.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)nc(Cl)c1NC(=O)c1cc(Br)cnc1Cl
Reaction #2316511
title compound
Rendimiento 36.4%DOI: 10.6084/m9.figshare.5104873.v1
Página 1Siguiente