مشارك في 633 تفاعل

3182

CCOC(=O)c1ccc(NC(=O)c2ccccc2C)cc1
Reaction #3592
ethyl 4-[(2-methylbenzoyl)amino]benzoate
المردود 76.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc(N)c(Cl)c1
Reaction #3680
ethyl 3-chloro-4-aminobenzoate
المردود 73.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc(NN2CN(Nc3ccc(C(=O)OCC)cc3)CN(Nc3ccc(C(=O)OCC)cc3)C2)cc1
Reaction #4252
1,3,5-tris-(p-ethoxycarbonylanilino)-s-triazine
المردود 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCOC(=O)c1ccc(C2COC(OC)C2)cc1
Reaction #8295
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1ccc(N/C(=C2\C(=O)Nc3ccccc32)c2ccccc2)cc1
Reaction #53021
(Z)-3-[1-(4-ethoxycarbonyl-phenylamino)-1-phenyl-methylidene]-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)c1ccc2c(c1)C(SC)C(=O)N2
Reaction #72544
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1ccc(N)c(Cl)c1
Reaction #79432
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOC(=O)c1ccc(NC(=O)CC2CCc3cc(Br)cc4[nH]c(=O)c(=O)n2c34)cc1
Reaction #80780
title compound
المردود 47.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)c1ccc(NC(=O)C[C@H]2[C@H](C)Cc3cc(Br)cc4[nH]c(=O)c(=O)n2c34)cc1
Reaction #80814
title compound
المردود 82.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)c1ccc(NC(=O)c2ccccc2C)cc1
Reaction #83424
ethyl 4-[(2-methylbenzoyl)amino]benzoate
المردود 76.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)c1ccc(N)c(Cl)c1
Reaction #83501
ethyl 3-chloro-4-aminobenzoate
المردود 73.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCOC(=O)c1ccc(NC(=O)C(CCOC)n2cc(OC)c(-c3cc(Cl)ccc3C#N)cc2=O)cc1
Reaction #85049
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1cn(C(CC2CCOCC2)C(=O)Nc2ccc(C(=O)O)cc2)c(=O)cc1-c1cc(Cl)ccc1C#N
Reaction #85060
4-({2-[4-(5-Chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-(tetrahydro-2H-pyran-4-yl)propanoyl}amino)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)c1ccc(NC(=O)C(CC(F)F)n2cc(OC)c(-c3cc(Cl)ccc3C#N)cc2=O)cc1
Reaction #85075
Ethyl 4-({2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-4,4-difluorobutanoyl}amino)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)c1ccc(NC(=O)C(CC(F)(F)F)n2cc(OC)c(-c3cc(Cl)ccc3C#N)cc2=O)cc1
Reaction #85077
Ethyl 4-({2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-4,4,4-trifluorobutanoyl}amino)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)c1ccc(NC(=O)C(CC(C)F)n2cc(OC)c(-c3cc(Cl)ccc3C#N)cc2=O)cc1
Reaction #85080
Ethyl 4-({2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-4-fluoropentanoyl}amino)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)c1ccc(NC(=O)C(CC(CC)OC)n2cc(OC)c(-c3cc(Cl)ccc3C#N)cc2=O)cc1
Reaction #85145
Ethyl 4-({2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-4-methoxyhexanoyl}amino)-benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)c1ccc(NC(=O)C(CCO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)n2cc(OC)c(-c3cc(Cl)ccc3C#N)cc2=O)cc1
Reaction #85150
Ethyl 4-[(4-{[tert-butyl(diphenyl)silyl]oxy}-2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]butanoyl)amino]benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)c1ccc(NC(=O)C(CC2(C)CCOCC2)n2cc(OC)c(-c3cc(Cl)ccc3C#N)cc2=O)cc1
Reaction #85171
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)c1ccc(NC(=O)C(C[C@H]2CC[C@@H](OC)CC2)n2cc(OC)c(-c3cc(Cl)ccc3C#N)cc2=O)cc1
Reaction #85177
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
الصفحة 1التالي