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1346679

O=C(NC1CCC(Oc2ccc(F)cc2)CC1)NC12CC3CC(CC(C3)C1)C2
Reaction #176310
DOI: 10.1039/C8SC04228D
COc1ccc(C(OC2CN(C(=O)NC34CC5CC(CC(C5)C3)C4)C2)c2ccccc2C(F)(F)F)cc1
Reaction #198974
DOI: 10.1039/C8SC04228D
Cn1c(COc2ccc(CC3SC(=O)NC3=O)cc2)nc2ccc(Oc3cccc(NC(=O)NC45CC6CC(CC(C6)C4)C5)c3)cc21
Reaction #202254
DOI: 10.1039/C8SC04228D
CN1CCN(CCCNc2ncc3cc(-c4c(Cl)cccc4Cl)c(NC(=O)NC45CC6CC(CC(C6)C4)C5)nc3n2)CC1
Reaction #227104
DOI: 10.1039/C8SC04228D
Cn1c(COc2ccc(CC3SC(=O)NC3=O)cc2)nc2ccc(Oc3cccc(NC(=O)NC45CC6CC(CC(C6)C4)C5)c3)cc21
Reaction #499526
title compound
Выход 13.9%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Cn1c(COc2ccc(CC3SC(=O)NC3=O)cc2)nc2ccc(Oc3ccc(CCNC(=O)NC45CC6CC(CC(C6)C4)C5)cc3)cc21
Reaction #499531
title compound
Выход 152.9%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(COc2ccc(CC3SC(=O)NC3=O)cc2)nc2ccc(Oc3ccc4cccc(NC(=O)NC56CC7CC(CC(C7)C5)C6)c4c3)cc21
Reaction #499539
title compound
Выход 67.3%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1c(Cl)ccc(NC(=O)NC23CC4CC(CC(C4)C2)C3)c1O
Reaction #519787
desired product
Выход 56.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCNC(=O)NC12CC3CC(CC(C3)C1)C2
Reaction #531856
4-(3-adamantan-1-yl-ureido)butyric acid
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC12CC3CC(CC(C3)C1)C2)N[C@H]1CC[C@H](O)CC1
Reaction #531867
trans-1-(4-Hydroxy-cyclohexyl)-3-tricyclo[3.3.1.13,7]decan-1-yl-urea
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC12CC3CC(CC(C3)C1)C2)N[C@H]1CC[C@@H](Oc2ccc(F)cc2)CC1
Reaction #531872
cis-1-[4-(4-Fluoro-phenoxy)-cyclohexyl]-3-tricyclo[3.3.1.13,7]decan-1-yl-urea
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2cc(-c3ccc4c(c3)CN(C(=O)NC35CC6CC(CC(C6)C3)C5)CC4)nc(N)n2)CC1
Reaction #536548
N-1-Adamantyl-7-[2-amino-6-(4-methylpiperazin-1-yl)pyrimidin-4-yl]-3,4-dihydroisoquinoline-2(1H)-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
O=c1sn(C23CC4CC(CC(C4)C2)C3)c(=O)n1Cc1ccccc1
Reaction #578875
2-(1-adamantyl)-4-benzyl-[1,2,4]thiadiazolidine-3,5-dione
DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc(-n2nc(CCCNC(=O)NC34CC5CC(CC(C5)C3)C4)cc2-c2ccccc2)cc1
Reaction #595792
titled compound
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(Oc2ccc(NC(=O)NC34CC5CC(CC(C5)C3)C4)cc2)ccn1
Reaction #659422
Compound 2287
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(C(OC2CN(C(=O)NC34CC5CC(CC(C5)C3)C4)C2)c2ccccc2C(F)(F)F)cc1
Reaction #765185
DOI: 10.1039/C8SC04228D
NS(=O)(=O)c1c(Cl)ccc(NC(=O)NC23CC4CC(CC(C4)C2)C3)c1O
Reaction #768933
DOI: 10.1039/C8SC04228D
O=C(NC12CC3CC(CC(C3)C1)C2)N1CC(OC(c2ccc(F)cc2)c2ccccc2C(F)(F)F)C1
Reaction #897276
DOI: 10.1039/C8SC04228D
CN1CCN(c2cc(-c3ccc4c(c3)CN(C(=O)NC35CC6CC(CC(C6)C3)C5)CC4)nc(N)n2)CC1
Reaction #914260
DOI: 10.1039/C8SC04228D
Cc1ccc(C(OC2CN(C(=O)NC34CC5CC(CC(C5)C3)C4)C2)c2ccccc2C(F)(F)F)cc1
Reaction #922330
DOI: 10.1039/C8SC04228D
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