Busqueda de Subestructura

1385439

O=C(O)c1ccncc1Nc1ccc(Cl)cc1Cl
Reaction #67777
desired product
Rendimiento 72.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Br)ccc1Nc1cnccc1C(=O)O
Reaction #67778
desired product
Rendimiento 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(I)ccc1Nc1cnccc1C(=O)O
Reaction #67779
desired product
Rendimiento 59.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc[n+]([O-])cc1F
Reaction #67786
3-fluoroisonicotinic acid 1-oxide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Br)ncc1Nc1ccc(I)cc1F
Reaction #67787
2-Bromo-5-(2-fluoro-4-iodo-phenylamino)-isonicotinic acid
Rendimiento 59.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Br)ncc1F
Reaction #67789
methyl 2-bromo-5-fluoroisonicotinate
Rendimiento 81.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(C)ncc1F
Reaction #67790
Methyl 5-fluoro-2-methylisonicotinate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)O)c(Nc2ccc(I)cc2F)cn1
Reaction #67791
5-[(2-fluoro-4-iodophenyl)amino]-2-methylisonicotinic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(-c2ccccc2)ncc1F
Reaction #67793
5-fluoro-2-phenylisonicotinic acid
Rendimiento 58.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(-c2ccccc2)ncc1Nc1ccc(I)cc1F
Reaction #67794
5-[(2-fluoro-4-iodophenyl)amino]-2-phenylisonicotinic acid
Rendimiento 56.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccncc1Nc1ccc(I)cc1Cl
Reaction #67796
3-[(2-chloro-4-iodophenyl)amino]isonicotinic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Nc2cnccc2C(=O)O)cc1
Reaction #67878
desired product
Rendimiento 13.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccncc1Nc1ccc(SC(F)(F)F)cc1
Reaction #67879
desired product
Rendimiento 10.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccncc1Nc1ccc(OC(F)(F)F)cc1
Reaction #67880
desired product
Rendimiento 9.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CCC(Oc2ccc3c(c2)CCC(c2ccccc2)O3)CC1)c1ccncc1F
Reaction #88058
title compound
Rendimiento 68.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1ccnc(Cl)c1F
Reaction #88221
tert-butyl N-(2-chloro-3-fluoro-4-pyridyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccncc1NCc1ccccc1F
Reaction #91310
title compound
Rendimiento 10.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccncc1NCc1cccc(F)c1
Reaction #91311
title compound
Rendimiento 33.2%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CNc2cnccc2C(=O)O)cc1
Reaction #91314
title compound
Rendimiento 18.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2cnccc2C(=O)O)cc1
Reaction #91316
title compound
Rendimiento 26.0%DOI: 10.6084/m9.figshare.5104873.v1
Página 1Siguiente