Recherche de Sous-structure

566210

COc1ccccc1C(C)NCc1ccc(CN(Cc2nc3ccccc3[nH]2)C2CCCc3cccnc32)cc1
Reaction #7266
desired product
Rendement 31.2%DOI: 10.6084/m9.figshare.5104873.v1
c1cnc2c(c1)CCCC2N(Cc1ccc(CNc2cc[nH]n2)cc1)Cc1nc2ccccc2[nH]1
Reaction #7276
amine
Rendement 23.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(-c2ccc(F)cc2)oc2ncc(-c3cc(C(=O)NC4(c5ccccn5)CC4)ccc3Cl)cc12
Reaction #72365
methyl 5-(2-chloro-5-(1-(pyridin-2-yl)cyclopropylcarbamoyl)phenyl)-2-(4-fluorophenyl)furo[2,3-b]pyridine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(-c2ccc(F)cc2)oc2ncc(-c3cc(C(=O)NC4(c5ccccn5)CC4)ccc3C)cc12
Reaction #72370
methyl 2-(4-fluorophenyl)-5-(2-methyl-5-(1-(pyridin-2-yl)cyclopropylcarbamoyl)phenyl)furo[2,3-b]pyridine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NC(Cn1ccnc1)c1ccc(Cl)cn1
Reaction #82793
1-Azido-1-(5-chloro-2-pyridyl)-2-(1H-imidazol-1-yl)ethane
DOI: 10.6084/m9.figshare.5104873.v1
NC(Cn1ccnc1)c1ccc(Cl)cn1
Reaction #82794
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(NC(C)c2ccccn2)nc(NC2CCCCC2)c1C
Reaction #91452
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Cl)ncc1F)c1nc2ccn(C)c2cc1-c1ccnn1C
Reaction #162467
title compound
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Nc2cc(C3CC3)[nH]n2)c(Cl)cc1C#N)c1ccc(F)cn1
Reaction #163068
title compound
Rendement 52.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](N)c1ccc(F)cn1
Reaction #163118
(S)-1-(5-Fluoropyridin-2-yl)ethanamine
Rendement 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1c(-c2ccc(F)cc2)oc2ccc(-c3cc(C(=O)NC4(c5ccccn5)CC4)c(OC)cc3OCC(N)=O)cc12
Reaction #182748
DOI: 10.1039/C8SC04228D
CC(Nc1ncc(Cl)c(Nc2cc(C3CC3)[nH]n2)n1)c1ccc(F)cn1
Reaction #191989
DOI: 10.1039/C8SC04228D
NC(Cn1ccnc1)c1ccc(Cl)cn1
Reaction #196136
DOI: 10.1039/C8SC04228D
Cc1cc(Nc2nc(NC(C)c3ccc(F)cn3)nc(N3CCOCC3)c2[N+](=O)[O-])n[nH]1
Reaction #205214
DOI: 10.1039/C8SC04228D
CC(c1cccnc1)N1CCN(c2c(Br)cnc(N)c2[N+](=O)[O-])CC1
Reaction #207354
DOI: 10.1039/C8SC04228D
CCC(CC)N1C(=O)CCC(c2cccc(Cl)c2)C1c1ccc(Cl)cn1
Reaction #208425
DOI: 10.1039/C8SC04228D
NCCN1CCN(C(c2ccc(C(F)(F)F)cc2)c2ccccn2)CC1
Reaction #216956
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(-c2ccccn2)nn1C(C)c1ccccn1
Reaction #217012
1-(1-(2-pyridinyl)ethyl)-3-(2-pyridinyl)pyrazole-5-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1c2cccnc2C(N2C(=O)c3ccccc3C2=O)CCC1c1cccc(F)c1F
Reaction #230043
DOI: 10.1039/C8SC04228D
C=CCC1(C)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(C(CC(F)F)c2ccccn2)C1=O
Reaction #232797
DOI: 10.1039/C8SC04228D
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