بحث البنية الفرعية

NC(=O)c1ccc(O)cc1

COc1ccc(C(=O)NC(CC(C)C)C(=O)O)c(SSc2cc(OC)ccc2C(=O)NC(CC(C)C)C(=O)O)c1
Reaction #3349
title compound
المردود 69.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1ccc(Oc2cc3nc(-c4nccs4)[nH]c3cc2Oc2ccccc2S(C)(=O)=O)cc1
Reaction #41517
5-(4-Dimethylcarbamoyl-phenoxy)-6-(2-methanesulfonyl-phenoxy)-2-thiazol-2-yl-1H-benzimidazole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)c2ccc(OC3CCN(C)CC3)c(C(F)(F)F)c2)cc1Nc1nccc(-c2cccnc2)n1
Reaction #42074
4-(1-methylpiperidin-4-yloxy)-3-trifluoromethyl-N-{4-methyl-3-[4-(3-pyridyl)pyrimidin-2-ylamino]phenyl}benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CCn1ccc(NC(=O)c2cc(Oc3ccc(C(=O)N4CCC4)cc3)cc(O[C@@H](C)CO)c2)n1
Reaction #48806
product
المردود 73.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(NC(=O)c2cc(Oc3ccc(C(=O)N4CCC4)cc3F)cc(O[C@@H](C)CO)c2)s1
Reaction #48841
desired compound
المردود 11.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nn(C)c2c(=O)[nH]c(-c3cc(C(=O)N4CCN(C)CC4)ccc3OCC)nc12
Reaction #50212
title compound
المردود 25.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)N2CCOc3ccc(C4=NNC(=O)CC4)cc32)cc1OC
Reaction #63461
6-(3,4-Dihydro-4-(3,4-dimethoxyphenylcarbonyl)-1,4(2H)-benzoxazin-6-yl)-2,3,4,5-tetrahydropyridazin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)Nc2nc(C)c(C(=O)NCc3ccccc3)s2)cc1
Reaction #73635
title compound
المردود 10.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)c(C(N)=O)cc1CNC(=O)C(F)(F)F
Reaction #87648
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)c(C(=O)N=C=O)cc1CNC(=O)C(F)(F)F
Reaction #87649
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)cc1CNC(=O)C(F)(F)F
Reaction #87650
desired product
المردود 24.5%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #158169
solid
المردود 32.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC1CN(c2ccc(C(F)(F)F)cc2)CC2(CCN(C(=O)c3ccc(OC(C)C)c(C)c3)CC2)O1
Reaction #160237
(4-isopropoxy-3-methylphenyl)(2-(methoxymethyl)-4-(4-(trifluoromethyl)phenyl)-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)methanone
المردود 10.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1csc(NC(=O)c2cc(OC)c(OC)cc2O)n1
Reaction #165884
same compound ( 5a )
المردود 55.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1csc(NC(=O)c2cc(OC)c(OC)cc2O)n1
Reaction #165885
title compound ( 5a )
المردود 84.9%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)c1ccc2c(c1)-c1sc(C(=O)N(C)c3ccccc3Cl)cc1CCO2
Reaction #171762
300
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)c2ccc3c(c2)-c2sc(C(=O)N(C)c4ccc(Cl)cc4Cl)cc2CCO3)C[C@H](C)N1
Reaction #171825
360
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCO)c1ccc2c(c1)-c1sc(-c3nncn3-c3ccc(F)cc3F)cc1CCO2
Reaction #171829
375
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCO)c1ccc2c(c1)-c1sc(-c3ncnn3-c3ccc(F)cc3F)cc1CCO2
Reaction #171832
398
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1ccc2c(c1)-c1sc(C(=O)N(C)c3ccc(F)cc3F)cc1CO2
Reaction #171874
N2-(2,4-difluorophenyl)-N2,N8,N8-trimethyl-4H-thieno[3,2-c]chromene-2,8-dicarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي