Recherche de Sous-structure

NCC(O)CN

CSc1nccc(C(=O)N2CC(OC(=O)C(C)(C)C)CN2C(=O)Cc2ccc(F)cc2)n1
Reaction #7754
desired product
Rendement 96.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccc(F)cc1)N1CC(O)CN1C(=O)OCc1ccccc1
Reaction #7757
2-[2-(4-fluorophenyl)acetyl]-4-hydroxy-pyrazolidine-1-carboxylic acid benzyl ester
Rendement 73.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Oc1ccc([N+](=O)[O-])cc1)OC1CN(C(=O)Cc2ccc(F)cc2)N(C(=O)OCc2ccccc2)C1
Reaction #7758
desired product
Rendement 86.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1CN(C(=O)Cc2ccc(F)cc2)N(C(=O)OCc2ccccc2)C1
Reaction #7763
desired product
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1CN(C(=O)Cc2ccc(F)cc2)N(C(=O)c2ccnc(SC)n2)C1
Reaction #7764
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COC1Cn2c(-c3ccnc(SC)n3)c(-c3ccc(F)cc3)c(=O)n2C1
Reaction #7765
desired product
Rendement 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(CCC)S(=O)(=O)C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](O)CNCc1cccc(CC)c1
Reaction #42337
N2-[(benzyloxy)carbonyl]-N1-{(1S,2R)-1-(3,5-difluorobenzyl)-3-[(3-ethylbenzyl)amino]-2-hydroxypropyl}-3-[(1-propylbutyl)sulfonyl]alaninamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)CNCc2cccc(CC)c2)cc(-c2ncc[nH]2)c1
Reaction #42342
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)CNCc2cccc(C(C)C)c2)cc(-c2nccs2)c1.Cl
Reaction #42366
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cccc(C2(NC[C@@H](O)[C@H](Cc3cc(F)cc(F)c3)NC(=O)c3cc(C)cc(CN(C)CCCC)c3)CC2)c1.Cl.Cl
Reaction #42390
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)Cc1cc(C)cc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)CNC2(c3ccccc3)CC2)c1.Cl.Cl
Reaction #42394
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cccc(C2(NC[C@@H](O)[C@H](Cc3cc(F)cc(F)c3)NC(=O)c3cc(CN(C)CCCC)cc(-c4ncco4)c3)CC2)c1.Cl.Cl
Reaction #42398
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCSc1cccc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)CNC2(c3cccc(CC)c3)CC2)c1
Reaction #42507
desired compound
Rendement 176.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)CNCc2cccc(CC)c2)cc(-c2nc(C)co2)c1
Reaction #42565
N1-{(1S,2R)-1-(3,5-difluorobenzyl)-3-[(3-ethylbenzyl)amino]-2-hydroxypropyl}-5-(4-methyl-1,3-oxazol-2-yl)-N3,N3-dipropylisophthalamide
Rendement 26.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C)C(=O)c1cc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)CNCc2cccc(CC)c2)cc(-c2ncco2)c1
Reaction #42574
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc(C2(NC[C@@H](O)[C@H](Cc3cc(F)cc(F)c3)NC(=O)CCCC(=O)O)CC2)c1
Reaction #42606
5-[((1S,2R)-1-(3,5-difluorobenzyl)-3-{[1-(3-ethylphenyl)cyclopropyl]amino}-2-hydroxypropyl)amino]-5-oxopentanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc(C2(NC[C@@H](O)[C@H](Cc3cc(F)cc(F)c3)NC(=O)CCC(=O)O)CC2)c1
Reaction #42607
4-[((1S,2R)-1-(3,5-difluorobenzyl)-3-{[1-(3-ethylphenyl)cyclopropyl]amino}-2-hydroxypropyl)amino]-4-oxobutanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N[C@@H](Cc2cc(F)cc(F)c2)[C@@H]([C@H]2C[C@H](O)CN2C(c2ccccc2)c2ccccc2)O1
Reaction #49215
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #49235
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)OC1CNN(C(=O)Cc2ccc(F)cc2)C1
Reaction #50961
desired product
Rendement 98.0%DOI: 10.6084/m9.figshare.5104873.v1
Page 1Suivant