子结构搜索

117189

Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)c(C(F)(F)F)c2)cc1N
Reaction #42057
objective compound
收率 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2ccc(C(=O)Nc3ccc(C)c(Nc4nccc(-c5cncc(Br)c5)n4)c3)cc2C(F)(F)F)CC1
Reaction #42061
4-(4-ethylpiperazin-1-ylmethyl)-3-trifluoromethyl-N-{3-[4-(5-bromopyridin-3-yl)pyrimidin-2-ylamino]-4-methylphenyl}benzamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)c(C(F)(F)F)c2)cc1Nc1cc(-c2cncnc2)ccn1
Reaction #42062
4-(4-methylpiperazin-1-ylmethyl)-3-trifluoromethyl-N-{4-methyl-3-[4-(5-pyrimidinyl)pyridin-2-ylamino]phenyl}benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2ccc(C(=O)Nc3ccc(C)c(Nc4cc(-c5cncnc5)ccn4)c3)cc2C(F)(F)F)CC1
Reaction #42063
4-(4-ethylpiperazin-1-ylmethyl)-3-trifluoromethyl-N-{4-methyl-3-[4-(5-pyrimidinyl)pyridin-2-ylamino]phenyl}benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2ccc(C(=O)Nc3ccc(C)c(Nc4cc(-c5cccnc5)ccn4)c3)cc2C(F)(F)F)CC1
Reaction #42064
objective compound
收率 22.4%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)O.Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)c(C(F)(F)F)c2)cc1Nc1cc(-c2cccnc2)ccn1
Reaction #42065
objective compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)c(C(F)(F)F)c2)cc1Nc1cc(-c2cccnc2)ncn1
Reaction #42066
4-(1-methylpiperazin-4-ylmethyl)-3-trifluoromethyl-N-{4-methyl-3-[6-(3-pyridyl)pyrimidin-4-ylamino]phenyl}benzamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)c(C(F)(F)F)c2)cc1Nc1cc(-c2cncnc2)ncn1
Reaction #42067
4-(1-methylpiperazin-4-ylmethyl)-3-trifluoromethyl-N-{4-methyl-3-[6-(5-pyrimidinyl)pyrimidin-4-ylamino]phenyl}benzamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)c2ccc(CN3CCN(CCF)CC3)c(C(F)(F)F)c2)cc1Nc1nccc(-c2cncnc2)n1
Reaction #42068
objective compound
收率 55.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)c2ccc(CN3CCN(C(=O)OC(C)(C)C)CC3)c(C(F)(F)F)c2)cc1Nc1nccc(-c2cncc(Br)c2)n1
Reaction #42069
4-[4-(t-butoxycarbonyl)piperazin-1-ylmethyl]-3-trifluoromethyl-N-{3-[4-(5-bromopyridin-3-yl)pyrimidin-2-ylamino]-4-methylphenyl}benzamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)c2ccc(CN3CCN(C(=O)OC(C)(C)C)CC3)c(C(F)(F)F)c2)cc1Nc1cc(-c2cccnc2)ccn1
Reaction #42070
4-[4-(t-butoxycarbonyl)piperazin-1-ylmethyl]-3-trifluoromethyl-N-{4-methyl-3-[4-(3-pyridyl)pyridin-2-ylamino]phenyl}benzamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)c(C(F)(F)F)c2)cc1Nc1nc(-c2ccncc2)cs1
Reaction #42073
objective compound
收率 82.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)c(C(F)(F)F)c2)cc1Nc1cc(-c2cccnc2)ccn1
Reaction #174427
DOI: 10.1039/C8SC04228D
CCN1CCN(Cc2ccc(C(=O)Nc3ccc(C)c(Nc4cc(-c5cncnc5)ccn4)c3)cc2C(F)(F)F)CC1
Reaction #194753
DOI: 10.1039/C8SC04228D
Cc1ccc(NC(=O)c2ccc(CN3CCN(C(=O)OC(C)(C)C)CC3)c(C(F)(F)F)c2)cc1Nc1nccc(-c2cncc(Br)c2)n1
Reaction #209698
DOI: 10.1039/C8SC04228D
Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)c(C(F)(F)F)c2)cc1Nc1cc(-c2cccnc2)ncn1
Reaction #272619
DOI: 10.1039/C8SC04228D
Cc1ccc(NC(=O)c2ccc(CN3CCN(C(=O)OC(C)(C)C)CC3)c(C(F)(F)F)c2)cc1Nc1nccc(-c2cncnc2)n1
Reaction #280130
DOI: 10.1039/C8SC04228D
Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)c(C(F)(F)F)c2)cc1N
Reaction #295311
DOI: 10.1039/C8SC04228D
Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)c(C(F)(F)F)c2)cc1Nc1nccc(-c2cncnc2)n1
Reaction #299687
DOI: 10.1039/C8SC04228D
CCN1CCN(Cc2ccc(C(=O)Nc3ccc(C)c(Nc4nccc(-c5cncc(Br)c5)n4)c3)cc2C(F)(F)F)CC1
Reaction #372372
DOI: 10.1039/C8SC04228D
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