Busqueda de Subestructura

718800

Cc1cc(-c2ccc(CC(=O)Nc3ccc(I)cn3)cc2)ccn1
Reaction #245813
DOI: 10.1039/C8SC04228D
CCN1N(c2ccc(I)cn2)C(=O)CC1(C)C
Reaction #327669
1-ethyl-2-(5-iodo-pyridin-2-yl)-5,5-dimethyl-pyrazolidin-3-one
Rendimiento 28.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC(C)(C)C(=O)Nc1ccc(I)cn1
Reaction #378737
DOI: 10.1039/C8SC04228D
CC(C)(C)C(=S)Nc1ccc(I)cn1
Reaction #396591
DOI: 10.1039/C8SC04228D
COc1ccccc1Nc1ccc(NC(=O)C2(c3ccc4c(c3)OCO4)CC2)nc1
Reaction #425770
1-(benzo[d][1,3]dioxol-5-yl)-N-(5-(2-methoxyphenylamino)pyridin-2-yl)cyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C[C@H]2CCC[C@H]2N1c1ccc(I)cn1
Reaction #607975
title compound
Rendimiento 55.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C[C@H]2CCC[C@H]2N1c1ccc(C#Cc2ccccc2)cn1
Reaction #607976
title compound
Rendimiento 96.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C[C@H]2CCC[C@H]2N1c1ccc(C#Cc2cccc(F)c2)cn1
Reaction #607977
title compound
Rendimiento 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C[C@H]2CCC[C@H]2N1c1ccc(C#Cc2ccc(F)cc2)cn1
Reaction #607978
title compound
Rendimiento 77.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C[C@H]2CCC[C@H]2N1c1ccc(C#Cc2cc(F)ccc2F)cn1
Reaction #607979
title compound
Rendimiento 98.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccc(CC(=O)Nc3ccc(-c4cn[nH]c4)cn3)cc2)ccn1
Reaction #679325
N-(5-(1H-pyrazol-4-yl)pyridin-2-yl)-2-(4-(2-methylpyridin-4-yl)phenyl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)N(c2ccc(I)cn2)C1=O
Reaction #716389
1-(5-iodopyridin-2-yl)-3,3-dimethylpyrrolidine-2,5-dione
Rendimiento 86.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)N(c2ccc(I)cn2)C1O
Reaction #716390
(5-RS)-5-hydroxy-1-(5-iodo-pyridin-2-yl)-4,4-dimethyl-pyrrolidin-2-one
Rendimiento 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)N(c2ccc(I)cn2)C1
Reaction #716391
1-(5-iodopyridin-2-yl)-4,4-dimethylpyrrolidin-2-one
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #716393
solid
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CC1NC(C(=O)Nc2ccc(I)cn2)C(c2cccc(Cl)c2F)C1(C#N)c1ccc(Cl)cc1F
Reaction #749435
DOI: 10.1039/C8SC04228D
CC(C)(C)C(=O)Nc1ccc(I)cn1
Reaction #768299
DOI: 10.1039/C8SC04228D
Cc1cc(-c2ccc(CC(=O)Nc3ccc(-c4cn[nH]c4)cn3)cc2)ccn1
Reaction #782023
DOI: 10.1039/C8SC04228D
CC1(C)C(=O)N(c2ccc(I)cn2)C(=O)C1O[Si](c1ccccc1)(c1ccccc1)C(C)(C)C
Reaction #1035263
DOI: 10.1039/C8SC04228D
Cc1cc(-c2ccc(CC(=O)Nc3ccc(I)cn3)cc2)ccn1
Reaction #1123366
N-(5-iodopyridin-2-yl)-2-(4-(2-methylpyridin-4-yl)phenyl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1
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