Substructure Search

CNc1ccc(F)cc1

CCOC(=O)[C@@H](C)Nc1ccc(F)c(F)c1F
Reaction #8543
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1COc2c(ccc(F)c2F)N1
Reaction #8577
title compound
Yield 66.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1COc2c(ccc(F)c2F)N1
Reaction #8578
title compound
Yield 79.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1COc2c(ccc(F)c2F)N1
Reaction #8579
title compound
Yield 99.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN1c2ccc(F)c(F)c2OC[C@@H]1C)C(=O)OCC
Reaction #8580
title compound
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN1c2ccc(F)c(F)c2OC[C@@H]1C)C(=O)OCC
Reaction #8581
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1COc2c(ccc(F)c2F)N1C(=O)C=NO
Reaction #10434
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CCN(Cc2cc(Oc3ccc4c(ccn4C(=O)Nc4ccc(F)c(C(F)(F)F)c4)c3)ncn2)CC1
Reaction #73392
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCN(C(=O)c1ccc2c(c1)nc(CNc1ccc(C(=N)N)cc1)n2C)c1ccc(F)cc1.Cl
Reaction #78669
1-Methyl-2-[N-(4-amidinophenyl)aminomethyl]benzimidazol-5-yl-carboxylic acid-N-(4-fluorophenyl)-N-(2-ethoxycarbonylethyl)amide hydrochloride
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(N2CCOCC2)ccc1F
Reaction #84404
title compound
Yield 57.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(=O)n(-c2cc(N3CCOCC3)ccc2F)c(C)n1
Reaction #84405
title compound
Yield 69.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Nc1cc(N2CCN(C(=O)[C@H]3CCCCN3)CC2)ccc1F)c1ccc(Cl)cc1Cl
Reaction #162316
desired product
Yield 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(c2ccc(F)c(-c3nc4cc(C)ccc4n3C(=O)OC(C)(C)C)c2)CC1
Reaction #164263
title compound
Yield 99.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(c2ccc(F)c(-c3nc4cc(Cl)ccc4n3C(=O)OC(C)(C)C)c2)CC1
Reaction #164265
title compound
Yield 24.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(O)C1CCN(c2ccc(F)c(-c3nc4cc(Cl)ccc4[nH]3)c2)CC1
Reaction #164266
title compound
Yield 138.1%DOI: 10.6084/m9.figshare.5104873.v1
NC1=NC2(c3cc(NC(=O)c4ccc(F)cn4)ccc3F)CN(c3ncc(F)cn3)CC2CS1
Reaction #164773
title compound
Yield 186.9%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NC1=N[C@@]2(c3cc(NC(=O)c4ccc(F)cn4)ccc3F)CN(c3ncc(F)cn3)C[C@H]2CS1
Reaction #164776
title compound
Yield 38.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc(C(=O)Nc2ccc(F)c([C@]34CN(c5ncc(F)cn5)C[C@H]3CSC(N)=N4)c2)cn1.Cl
Reaction #164777
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#Cc1ccc(C(=O)Nc2ccc(F)c([C@]34CN(c5ncc(F)cn5)C[C@H]3CSC(N)=N4)c2)nc1
Reaction #164780
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NC1=N[C@@]2(c3cc(NC(=O)c4ncc(F)cc4F)ccc3F)CN(c3ncc(F)cn3)C[C@H]2CS1
Reaction #164781
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Page 1Next