Teilstruktursuche

1207065

COC(=O)c1c(CN2CCN(C)CC2)nc(-c2ccccc2)nc1-c1cccc([N+](=O)[O-])c1
Reaction #4784
methyl 6-(4-methylpiperazin-1-ylmethyl)-4-(3-nitrophenyl)-2-phenyl-5-pyrimidinecarboxylate
Ausbeute 23.6%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1ccnc(NCCCN2CCN(c3cccc(Cl)c3)CC2)n1.Cl
Reaction #5436
base
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(N[C@H]1CN2CCC1CC2)c1cc2cccn2cn1
Reaction #53434
product
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(NC(=O)n2ccc3cc(Oc4ncnc5c4CNC5)ccc32)cc(C(F)(F)F)c1
Reaction #73355
5-(6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-4-yloxy)-indole-1-carboxylic acid (3-methoxy-5 trifluoromethyl-phenyl)-amide
DOI: 10.6084/m9.figshare.5104873.v1
CC1NCc2ncnc(Oc3ccc4c(ccn4C(=O)Nc4cccc(C(F)(F)F)c4)c3)c21
Reaction #73374
racemic 5-(5-Methyl-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-4-yloxy)-indole-1-carboxylic acid (3-trifluoromethyl-phenyl)-amide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc(C(F)(F)F)c1)n1ccc2cc(Oc3ncnc4c3CN(CCO)C4)ccc21
Reaction #73377
5-(6-(2-hydroxyethyl)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-4-yloxy)-N-(3-(trifluoromethyl)phenyl)-1H-indole-1-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(F)(F)F
Reaction #73378
TFA
Ausbeute 0.1%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)CN1Cc2ncnc(Oc3ccc4c(ccn4C(=O)Nc4cccc(C(F)(F)F)c4)c3)c2C1
Reaction #73379
5-(6-carbamoylmethyl-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-4-yloxy)-indole-1-carboxylic acid (3-trifluoromethyl-phenyl)-amide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CCN(Cc2cc(Oc3ccc4c(ccn4C(=O)Nc4ccc(F)c(C(F)(F)F)c4)c3)ncn2)CC1
Reaction #73392
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2nc([C@H](C)Nc3ccnc4[nH]cnc34)c(-c3cccc(F)c3)c(=O)n12
Reaction #86580
desired product
Ausbeute 10.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(Cl)ncn1)N1CCC2CCCCC21
Reaction #161692
(6-chloropyrimidin-4-yl)-(octahydroindol-1-yl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(Cl)ncn1)N1CCc2cc(Cl)ccc21
Reaction #161693
(5-chloro-2,3-dihydroindol-1-yl)-(6-chloropyrimidin-4-yl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(N2CCC(n3c(=O)[nH]c4ncccc43)CC2)ncn1)N1CCC2CCCCC21
Reaction #161810
1-{1-[6-(octahydroindole-1-carbonyl)-pyrimidin-4-yl]-piperidin-4-yl}-1,3-dihydroimidazo[4,5-b]pyridin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)CCN(C1CCN(c3cc(C(=O)N4CCc5ccccc54)ncn3)CC1)C(=O)N2
Reaction #161813
3-{1-[6-(2,3-dihydroindole-1-carbonyl)-pyrimidin-4-yl]-piperidin-4-yl}-7-methoxy-1,3,4,5-tetrahydro-1,3-benzodiazepin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(N2CCC(N3CCc4cc(Cl)ccc4NC3=O)CC2)ncn1)N1CCc2ccccc21
Reaction #161814
7-chloro-3-{1-[6-(2,3-dihydroindole-1-carbonyl)-pyrimidin-4-yl]-piperidin-4-yl}-1,3,4,5-tetrahydro-1,3-benzodiazepin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(N2CCC(n3c(=O)[nH]c4ncccc43)CC2)ncn1)N1CCc2cc(Cl)ccc21
Reaction #161815
1-{1-[6-(5-chloro-2,3-dihydroindole-1-carbonyl)-pyrimidin-4-yl]-piperidin-4-yl}-1,3-dihydro-imidazo[4,5-b]pyridin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(N2CCC(n3c(=O)[nH]c4ncccc43)CC2)ncn1)N1CCc2cc(Br)ccc21
Reaction #161816
1-{1-[6-(5-bromo-2,3-dihydro-indole-1-carbonyl)-pyrimidin-4-yl]-piperidin-4-yl}-1,3-dihydro-imidazo[4,5-b]pyridin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)CCN(C1CCN(c3cc(C(=O)N4CCC5CCCCC54)ncn3)CC1)C(=O)N2
Reaction #161834
7-methoxy-3-{1-[6-(octahydro-indol-1-carbonyl)-pyrimidin-4-yl]piperidin-4-yl}-1,3,4,5-tetra-hydro-1,3-benzodiazepin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(CNC(=O)c2nc3n(c(=O)c2O)CC2(CO)CCC3(NC(=O)C(=O)N(C)C)CC2)ccc1F
Reaction #162909
title compound
Ausbeute 55.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(CNC(=O)c2nc3n(c(=O)c2O)CC2(CC#N)CCC3(N(C)C(=O)C(=O)N(C)C)CC2)ccc1F
Reaction #162911
title compound
Ausbeute 19.3%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter