Recherche de Sous-structure

CNCCNC

CC[C@@H]1C(=O)N(C)c2cnc(-c3ccncc3CN)nc2N1C1CCCC1
Reaction #73132
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-c3ccncc3CNC(C)=O)nc2N1C1CCCC1
Reaction #73139
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-c3ccncc3CNC(=O)c3ccccc3)nc2N1C1CCCC1
Reaction #73140
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-c3ccncc3CNS(C)(=O)=O)nc2N1C1CCCC1
Reaction #73141
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-c3ccncc3CNS(=O)(=O)c3ccccc3)nc2N1C1CCCC1
Reaction #73142
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N(C(=O)CN(C)C)S(=O)(=O)c2ccc3c(ccn3C)c2)cc(OC)c1OC
Reaction #78400
desired product
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCN(CCC(=O)Nc2cccc(-c3nc(Nc4ccc5[nH]ncc5c4)c4ccccc4n3)c2)CC1
Reaction #89831
N-(3-(4-(1H-indazol-5-ylamino)quinazolin-2-yl)phenyl)-3-(4-isopropylpiperazin-1-yl)propanamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nc(-c3ccc(-c4ccccc4)c(F)c3)nc(Nc3ccc4[nH]ncc4c3)c2cc1OCCN1CCN(C)CC1
Reaction #89891
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nc(-c3cccc(-c4ccccc4)c3)nc(Nc3ccc4[nH]ncc4c3)c2cc1OCCN1CCN(C)CC1
Reaction #89903
2-[(3-phenyl)phenyl)-N-(1H-indazol-5-yl)-7-methoxy-6-(2-(4-methylpiperazin-1-yl)ethoxy)quinazolin-4-amine
Rendement 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(C)[nH]c(=O)c1CNC(=O)c1cc(-c2ccc(N3CCN(C)CC3)nc2)cc2c1c(C)nn2C(C)C
Reaction #172687
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2nc(N3CCOCC3)c3cc(CN4CCN(S(C)(=O)=O)CC4)sc3n2)cnc1C
Reaction #174619
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CCC(N2CC(NC(=O)CNc3nn(C)c4ccc(C(O)C(F)(F)F)cc34)C2)CC1
Reaction #174933
DOI: 10.1039/C8SC04228D
O=C(c1ccc(-c2cnc3c(c2)N(Cc2cc(Cl)ccc2C(F)(F)F)CCN3)cc1)N1CCN(c2cccc(C(F)(F)F)c2)CC1
Reaction #177157
DOI: 10.1039/C8SC04228D
O=C(c1cccc(-c2cnc3c(c2)N(Cc2cc(Cl)ccc2C(F)(F)F)CCN3)c1)N1CCN(c2ccccc2)CC1
Reaction #200822
DOI: 10.1039/C8SC04228D
CC(C)NC(=O)CN1CCN(C(=O)c2cccc(-c3cnc4c(c3)N(Cc3cc(Cl)ccc3C(F)(F)F)CCN4)c2)CC1
Reaction #203223
DOI: 10.1039/C8SC04228D
Cc1ccc(S(=O)(=O)N2CCNC(=O)C2CC(=O)NC2CCCc3cc(-c4ccccc4-c4nc(C)no4)ccc32)cc1
Reaction #208130
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #208932
DOI: 10.1039/C8SC04228D
COC(=O)C1(CCCN2CCN(c3ccccc3)CC2)Sc2cc(Cl)ccc2OCC1=O
Reaction #209818
DOI: 10.1039/C8SC04228D
CN1CCN(C(=O)c2ccc(C(c3cc(F)ccc3F)S(=O)(=O)c3ccc(Cl)cc3)nc2)CC1
Reaction #212987
DOI: 10.1039/C8SC04228D
CCN1CCN(c2ccc(Nc3ncc4scc(-c5ccccc5C(F)(F)F)c4n3)cn2)CC1
Reaction #213790
DOI: 10.1039/C8SC04228D
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