部分構造検索

18999

N#Cc1c(F)cccc1Oc1ccc(N)cc1Cl
Reaction #44697
2-(4-Amino-2-chlorophenoxy)-6-fluorobenzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(F)ccc1CCn1ccn2c(=O)cc(-c3ccncn3)nc12
Reaction #62028
1-[2-(4-Fluoro-2-methoxy-phenyl)-ethyl]-7-(pyrimidin-4-yl)-1H-imidazo[1,2-a]pyrimidin-5-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccncc1)c1ccc(OCc2ccc3ccccc3n2)c(F)c1F
Reaction #62129
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2ccncc2)c(-c2ccc(OCc3ccc4ccccc4n3)c(F)c2F)n1
Reaction #62130
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN(c2nncs2)S(=O)(=O)c2cc(Cl)c(Oc3cc(F)c(C(F)(F)F)cc3-c3ccnnc3)cc2F)c(OC)c1
Reaction #74548
5-chloro-N-(2,4-dimethoxybenzyl)-2-fluoro-4-[5-fluoro-2-pyridazin-4-yl-4-(trifluoromethyl)phenoxy]-N-1,3,4-thiadiazol-2-ylbenzenesulfonamide
収率 23.0%DOI: 10.6084/m9.figshare.5104873.v1
Oc1cc(F)c(C(F)(F)F)cc1-c1ccnnc1
Reaction #74676
product
収率 62.5%DOI: 10.6084/m9.figshare.5104873.v1
C#CCN1C(=O)COc2cc(F)c(NN=CC(=O)C(F)(F)F)cc21
Reaction #76759
7-fluoro-6-trifluoroacetylmethylidenhydrazino-4-propargyl-2H-1,4-benzoxazin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc2c(c1)Oc1cc(F)c(Br)cc1N=C2
Reaction #175748
DOI: 10.1039/C8SC04228D
COc1ccc(NC(=O)c2c[nH]c3cccc(O)c23)c(F)c1
Reaction #179271
DOI: 10.1039/C8SC04228D
N#Cc1ccc(OCCCC2CCN(CCCOc3ccc(C#N)c(F)c3)CC2)cc1
Reaction #179532
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)c1cc(Cl)c(Oc2cnc(C3CC3)c(Cl)c2)cc1F
Reaction #184362
DOI: 10.1039/C8SC04228D
Fc1cc(OC(F)(F)C(F)F)cc(C(Cc2ccccc2)(NC2=NC3CCCC3O2)c2ccc(Cl)cn2)c1
Reaction #185246
DOI: 10.1039/C8SC04228D
CCC(CC(O)(C=Nc1cc(F)cc2[nH]c(=O)ccc12)C(F)(F)F)c1ccc(F)c(C)c1OC
Reaction #190833
DOI: 10.1039/C8SC04228D
COc1cn(-c2cc3c(cc2F)OC(F)(F)C(F)(F)O3)nc(-c2ccnn2-c2ccccc2)c1=O
Reaction #209625
DOI: 10.1039/C8SC04228D
COc1cc(F)c(N2C[C@@H](C)N[C@@H](C)C2)cc1N
Reaction #217596
title compound ( D18 )
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(F)c1Oc1cc(CN2CCN(C)CC2)ccc1NC(=O)Nc1nccs1
Reaction #219154
1-[2-(2-Fluoro-6-methoxy-phenoxy)-4-(4-methyl-piperazin-1-ylmethyl)-phenyl]-3-thiazol-2-yl-urea
収率 667.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(F)ccc1CCn1ccn2c(=O)cc(-c3ccncn3)nc12
Reaction #225143
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(C(C)NC(=O)c2cc(Cl)ccc2Oc2cc(F)cc(F)c2)cc1
Reaction #226279
DOI: 10.1039/C8SC04228D
COc1cc(F)c(F)cc1-c1ccc(OCc2cccc3[nH]ccc23)cc1
Reaction #233732
DOI: 10.1039/C8SC04228D
N#CC(=Cc1ccccc1)C(=O)Oc1c(F)c(F)c(F)c(F)c1F
Reaction #234773
DOI: 10.1039/C8SC04228D
1 ページ次のページ