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559821

Nc1ccc(N2CCOCC2)nc1
Reaction #67599
6-Morpholinopyridin-3-amine
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(Nc2ccc(N3CCN(C)CC3)nc2)nc1Nc1ccc2oc(=O)[nH]c2c1
Reaction #67601
N4-(benzoxazolin-2-on-5-yl)-N2-[2-(4-methylpiperazin-1-yl)pyridin-5-yl]-5-methylpyrimidine-2,4-diamine
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(Nc3ncc(F)c(Nc4ccc5[nH]c(=O)[nH]c5c4)n3)cn2)CC1
Reaction #67602
N4-(Benzimidazolin-2-on-5-yl)-N2-[2-(4-methylpiperazin-1-yl)pyridin-5-yl]-5-fluoropyrimidine-2,4-diamine
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(Nc2ccc(N3CCN(C)CC3)nc2)nc1Nc1ccc2[nH]c(=O)oc2c1
Reaction #67603
6-(5-Methyl-2-(6-(4-methylpiperazin-1-yl)pyridin-3-ylamino)pyrimidin-4-ylamino)benzo[d]oxazol-2(3H)-one
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(N2CCOCC2)nc1
Reaction #69799
6-Morpholinopyridin-3-amine
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(Nc2ccc(N3CCN(C)CC3)nc2)nc1Nc1ccc2oc(=O)[nH]c2c1
Reaction #69801
N4-(benzoxazolin-2-on-5-yl)-N2-[2-(4-methylpiperazin-1-yl)pyridin-5-yl]-5-methylpyrimidine-2,4-diamine
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(Nc3ncc(F)c(Nc4ccc5[nH]c(=O)[nH]c5c4)n3)cn2)CC1
Reaction #69802
N4-(Benzimidazolin-2-on-5-yl)-N2-[2-(4-methylpiperazin-1-yl)pyridin-5-yl]-5-fluoropyrimidine-2,4-diamine
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(Nc2ccc(N3CCN(C)CC3)nc2)nc1Nc1ccc2[nH]c(=O)oc2c1
Reaction #69803
6-(5-Methyl-2-(6-(4-methylpiperazin-1-yl)pyridin-3-ylamino)pyrimidin-4-ylamino)benzo[d]oxazol-2(3H)-one
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(NC(=O)c3ccc(-c4cccc5ccccc45)c4nccnc34)cn2)CC1
Reaction #71358
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(NC(=O)c3ccc(-c4cncc5ccccc45)c4nccnc34)cn2)CC1
Reaction #71365
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(NC(=O)c3ccc(-c4csc5ccccc45)c4nccnc34)cn2)CC1
Reaction #71367
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cscc1-c1ccc(C(=O)Nc2ccc(N3CCN(C)CC3)nc2)c2nccnc12
Reaction #71374
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(C)c1-c1ccc(C(=O)Nc2ccc(N3CCN(C)CC3)nc2)c2nccnc12
Reaction #71379
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2ccc(NC(=O)c3ccc(-c4c(F)c(OC)cc(OC)c4F)c4nccnc34)cn2)CC1
Reaction #71391
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2ccc(NC(=O)c3ccc(-c4c(Cl)c(OC)cc(OC)c4Cl)c4cccnc34)cn2)CC1
Reaction #71481
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(N2CCOCC2)nc1
Reaction #84428
title compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(=O)n(-c2ccc(N3CCOCC3)nc2)c(C)n1
Reaction #84429
title compound
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(NC(=O)OCC(Cl)(Cl)Cl)cn2)CC1
Reaction #180807
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(N2CCOCC2)nc1)c1nc(-c2ccccc2)oc1Br
Reaction #192079
DOI: 10.1039/C8SC04228D
Cc1cnc(Nc2ccc(N3CCN(C)CC3)nc2)nc1Nc1ccc2oc(=O)[nH]c2c1
Reaction #198869
DOI: 10.1039/C8SC04228D
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