Recherche de Sous-structure

5064

N=C(N)NCc1ccccc1CN(Cc1nc2ccccc2[nH]1)C1CCCc2cccnc21
Reaction #9020
desired product
Rendement 92.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N=C(NCc1ccc(CN(Cc2nc3ccccc3[nH]2)C2CCCc3cccnc32)cc1)NC(=O)OC(C)(C)C
Reaction #9021
N′,N″-di-t-butoxycarbonyl-N-(4-{[(1H-benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydroquinolin-8-yl)-amino]-methyl}-benzyl)-guanidine
Rendement 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(Nc3c(Cl)cncc3Cl)cc(=O)oc2c1OCCCCCNC(=N)N
Reaction #48981
1-(5-(4-(3,5-dichloropyridin-4-ylamino)-7-methoxy-2-oxo-2H-chromen-8-yloxy)pentyl)guanidine
DOI: 10.6084/m9.figshare.5104873.v1
NSOOc1ccc(-n2nc(C(N)=O)c3c2-c2cc([N+](=O)[O-])ccc2CC3)cc1
Reaction #51255
solid
Rendement 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nn(-c2ccc(OOSN)cc2)c2c1CCc1ccc(N)cc1-2
Reaction #51256
title compound
Rendement 85.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nn(-c2cccc(S(N)(=O)=O)c2)c2c1CCc1ccc([N+](=O)[O-])cc1-2
Reaction #51260
Ethyl 1-[3-(aminosulfonyl)phenyl]-8-nitro-4,5-dihydro-1H-benzo[g]indazole-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Cn1ncc2ccc3c(c21)O[C@@H](CN=[N+]=[N-])CO3)NC(=O)OC(C)(C)C
Reaction #59646
oil
Rendement 89.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](N[S@](=O)C(C)(C)C)c1ccn(-c2ccc(Cl)cc2)n1
Reaction #85720
(R)—N—((R)-1-(1-(4-chlorophenyl)-1H-pyrazol-3-yl)ethyl)-2-methylpropane-2-sulfinamide
Rendement 49.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](N)c1ccn(-c2ccc(Cl)cc2)n1
Reaction #85721
product
Rendement 83.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](N[S@](=O)C(C)(C)C)c1ccn(-c2ccc(Cl)cc2)n1
Reaction #85722
(R)—N—((R)-1-(1-(4-chlorophenyl)-1H-pyrazol-3-yl)ethyl)-2-methylpropane-2-sulfinamide
Rendement 45.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1nc2ccccc2n2ncc(C(=O)O)c12
Reaction #94051
4-Ethoxypyrazolo[1,5-a]quinoxaline-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2ccc3ncc(Cc4cc5cccnc5cc4C(F)(F)F)n3n2)cn1
Reaction #156390
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)/N=C(/NCc1cccc(OCC2CCCCC2)c1)NC(=O)OC(C)(C)C
Reaction #161615
(Z)-tert-butyl(tert-butoxycarbonylamino)(3-(cyclohexylmethoxy)benzylamino)methylenecarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N=C(NC(=O)OC(C)(C)C)N[C@@H]1CCC[C@H](Nc2nc(Cl)ncc2F)C1
Reaction #162221
tert-butyl (tert-butoxycarbonylamino)((1R,3S)-3-(2-chloro-5-fluoropyrimidin-4-ylamino)cyclohexylamino)methylenecarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(Cc2cnn(Cc3ccc(OC)cc3)c2)c2cccc(NC(=O)c3cnc4ccccn34)c12
Reaction #166495
product
Rendement 64.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2cc(C(F)(F)F)n3ncc(C#Cc4ccc(N)nc4)c3n2)ccc1C(F)(F)F
Reaction #177553
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2nc3ccc(C)cn3c2CC(=O)c2c(C)nn(C)c2C)cc1
Reaction #182874
DOI: 10.1039/C8SC04228D
COCCCn1ncc2ccc(CC(CC(NC(=O)OC(C)(C)C)C(O)CC(COCc3ccccc3)C(C)C)C(C)C)cc21
Reaction #199099
DOI: 10.1039/C8SC04228D
COc1nc2cc(-c3ccc4ncc5c(c4c3)n(-c3cn(C)nc3C)c(=O)n5C)cnc2n1C
Reaction #201261
DOI: 10.1039/C8SC04228D
CC(C)COc1ccc(-n2cc(C(=O)O)cn2)cc1C#N
Reaction #204046
DOI: 10.1039/C8SC04228D
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