部分構造検索

1351688

CCC(Oc1ccc(C(C)(C)CC)cc1C(C)(C)CC)C(=O)N1C(=O)COc2cc(NC(=O)Nc3ccc(C(F)(F)F)cc3)c(O)cc21
Reaction #62983
( h )
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(C(F)(F)F)cc1)Nc1cccc(-c2nn3c(c2-c2ccncc2)SCC3)c1
Reaction #66352
1-[3-(7-pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazol-6-yl)-phenyl]-3-(4-trifluoromethyl-phenyl)-urea
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(C(F)(F)F)cc1)Nc1cccc(-c2nn3ccsc3c2-c2ccncc2)c1
Reaction #66372
oil
収率 97.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1csc2c(-c3ccncc3)c(-c3cccc(NC(=O)Nc4ccc(C(F)(F)F)cc4)c3)nn12
Reaction #66374
7-pyridin-4-yl-6-{3-[3-(4-trifluoromethyl-phenyl)-ureido]-phenyl}-pyrazolo[5,1-b]thiazole-3-carboxylic acid ethyl ester
収率 61.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(C(F)(F)F)cc1)Nc1cccc(-c2n[nH]cc2-c2ccncc2)c1
Reaction #74092
desired product
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2cc(-c3ccnc(NC(C)(C)C)c3)c(-c3cccc(NC(=O)Nc4ccc(C(F)(F)F)cc4)c3)n2)cc1
Reaction #74117
title compound
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2cc(-c3ccnc(NC(C)(C)C)c3)c(-c3cccc(NC(=O)Nc4ccc(C(F)(F)F)cc4)c3)n2)cc1
Reaction #74137
title compound
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CNc1cc(-c2cn(Cc3ccc(OC)cc3)nc2-c2cccc(NC(=O)Nc3ccc(C(F)(F)F)cc3)c2)ccn1
Reaction #74144
title compound
収率 63.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2cc(-c3ccnc(N)n3)c(-c3cccc(NC(=O)Nc4ccc(C(F)(F)F)cc4)c3)n2)cc1
Reaction #74155
title compound
収率 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccc(OC)c(COC(=O)Nc2ccc(C(F)(F)F)cc2)c1)C(=O)OC
Reaction #174541
DOI: 10.1039/C8SC04228D
COc1cc2nccc(Oc3ccc(NC(=O)Nc4ccc(C(F)(F)F)cc4)cc3)c2cc1OC
Reaction #174638
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(C(F)(F)F)cc1)Nc1nc(OCC(F)(F)F)cc(C(F)(F)F)n1
Reaction #174941
DOI: 10.1039/C8SC04228D
CC1C(=O)N(CCCC(=O)N2CCC3(CC3)C(O)C2)CCN1C(=O)Nc1ccc(C(F)(F)F)cc1
Reaction #176558
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(C(F)(F)F)cc1)NC(Cc1ccc(C(F)(F)F)cc1)C(O)c1ccc(F)cc1
Reaction #182609
DOI: 10.1039/C8SC04228D
COc1cc2ncnc(Sc3cccc(NC(=O)Nc4ccc(C(F)(F)F)cc4)c3)c2cc1OC
Reaction #187684
DOI: 10.1039/C8SC04228D
N#Cc1c(Oc2cc(NC(=O)Nc3ccc(C(F)(F)F)cc3)c(F)cc2Cl)ccc2nc(NC(=O)C3CC3)sc12
Reaction #190321
DOI: 10.1039/C8SC04228D
Cn1c2c(c(-c3cccc(NC(=O)Nc4ccc(C(F)(F)F)cc4)c3)c1-c1ccnc(N)n1)C(=O)N(C(=O)OC(C)(C)C)CC2
Reaction #190810
DOI: 10.1039/C8SC04228D
NC(=O)N(c1ccc(C(F)(F)F)cc1)c1nc(Cl)cc(Cl)n1
Reaction #199719
DOI: 10.1039/C8SC04228D
Cn1c(COc2ccc(CC3SC(=O)NC3=O)cc2)nc2ccc(OCCc3ccc(C(C)(C)C)c(NC(=O)Nc4ccc(C(F)(F)F)cc4)c3)cc21
Reaction #205613
DOI: 10.1039/C8SC04228D
NC(=O)c1[nH]c2cnccc2c1-c1ccc(NC(=O)Nc2ccc(C(F)(F)F)cc2)cc1
Reaction #208808
DOI: 10.1039/C8SC04228D
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