部分構造検索

794738

CCc1nn(Cc2cccc(O[C@@H]3CCN(C(=O)OC(C)(C)C)C[C@H]3F)n2)c2cccc(NC(=O)c3cnc4ccccn34)c12
Reaction #166487
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CO.ClCCl.[NH4+].[OH-]
Reaction #166488
DCM MeOH NH4OH
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cccc(OC3CCNCC3)n2)c2cccc(NC(=O)c3cnc4ccccn34)c12
Reaction #166489
desired product
収率 20.2%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2sc(-c3ccc(Cl)cc3)cc2cnn1Cc1cccc(OC2CCNCC2)n1
Reaction #188310
DOI: 10.1039/C8SC04228D
O=c1c2sc(-c3ccc(Cl)cc3)cc2ncn1Cc1cccc(OC2CCNCC2)n1
Reaction #199018
DOI: 10.1039/C8SC04228D
CN1CCC(Oc2cccc(Cn3ncc4cc(-c5ccc(Cl)cc5)sc4c3=O)n2)CC1
Reaction #750818
DOI: 10.1039/C8SC04228D
O=C(NC1CCN(Cc2ccncc2)CC1)c1cccc(OC2CCN(c3ccc(C(F)(F)F)cc3)CC2)n1
Reaction #792697
N-(1-(pyridin-4-ylmethyl)piperidin-4-yl)-6-(1-(4-(trifluoromethyl)phenyl)piperidin-4-yloxy)picolinamide
収率 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2cccc(Cn3ncc4cc(-c5ccc(Cl)cc5)sc4c3=O)n2)CC1
Reaction #894928
DOI: 10.1039/C8SC04228D
O=C(NC1CCN(Cc2ccncc2)CC1)c1cccc(OC2CCN(c3ccc(C(F)(F)F)cc3)CC2)n1
Reaction #1133693
N-(1-(pyridin-4-ylmethyl)piperidin-4-yl)-6-(1-(4-(trifluoromethyl)phenyl)piperidin-4-yloxy)picolinamide
収率 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2nc([C@H](C)Nc3ncnc4[nH]cnc34)cc3cccc(Cl)c23)CC1
Reaction #1138968
(S)—N-(1-(8-chloro-1-(1-isopropylpiperidin-4-yloxy)isoquinolin-3-yl)ethyl)-9H-purin-6-amine
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(Oc2cccc(CN)n2)CC1
Reaction #1220252
DOI: 10.1039/C8SC04228D
CC(C)N1CCC(Oc2nc([C@H](C)Nc3ncnc4[nH]cnc34)cc3cccc(Cl)c23)CC1
Reaction #1483800
(S)—N-(1-(8-chloro-1-(1-isopropylpiperidin-4-yloxy)isoquinolin-3-yl)ethyl)-9H-purin-6-amine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CCN(Cc2ccncc2)CC1)c1cccc(OC2CCN(c3ccc(C(F)(F)F)cc3)CC2)n1
Reaction #1730670
N-(1-(pyridin-4-ylmethyl)piperidin-4-yl)-6-(1-(4-(trifluoromethyl)phenyl)piperidin-4-yloxy)picolinamide
収率 25.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CCN(Cc2ccncc2)CC1)c1cccc(OC2CCN(c3ccc(C(F)(F)F)cc3)CC2)n1
Reaction #2213999
DOI: 10.1039/C8SC04228D
CN1CCC(Oc2cccc(CN)n2)CC1
Reaction #2326519
1-{6-[(1-Methylpiperidin-4-yl)oxy]pyridin-2-yl}methanamine
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(Oc2cccc(Cn3cnc4cc(-c5ccc(Cl)cc5)sc4c3=O)n2)CC1
Reaction #2326520
desired compound
収率 33.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2cccc(Cn3ncc4cc(-c5ccc(Cl)cc5)sc4c3=O)n2)CC1
Reaction #2326545
tert-Butyl 4-[(6-{[2-(4-chlorophenyl)-7-oxothieno[2,3-d]pyridazin-6(7H)-yl]methyl}pyridin-2-yl)oxy]piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2sc(-c3ccc(Cl)cc3)cc2cnn1Cc1cccc(OC2CCNCC2)n1
Reaction #2326546
2-(4-Chlorophenyl)-6-{[6-(piperidin-4-yloxy)pyridin-2-yl]methyl}thieno[2,3-d]pyridazin-7(6H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(Oc2cccc(Cn3ncc4cc(-c5ccc(Cl)cc5)sc4c3=O)n2)CC1
Reaction #2326547
2-(4-Chlorophenyl)-6-({6-[(1-methylpiperidin-4-yl)oxy]pyridin-2-yl}methyl)thieno[2,3-d]pyridazin-7(6H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2cccc(Cn3cnc4cc(-c5ccc(Cl)cc5)sc4c3=O)n2)CC1
Reaction #2326555
title compound
DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ