Ähnlichkeitssuche

406422

CC(C)(C)OC(=O)N1CCC2(CC1)CN(C1CCc3cc(-c4ncccn4)ccc31)C2
Reaction #177527
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2(CC1)CN(C1CCc3cc(-c4cnc(C(N)=O)cn4)ccc31)C2
Reaction #210408
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2(CC1)CN(C1CCc3cc(-n4nccn4)ccc31)C2
Reaction #229005
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2(CC1)CN(C1CCc3cc(-c4cnc(C#N)cn4)ccc31)C2
Reaction #244239
DOI: 10.1039/C8SC04228D
CCc1cnc(-c2ccc3c(c2)CCC3N2CC3(CCN(C(=O)OC(C)(C)C)CC3)C2)nc1
Reaction #299109
DOI: 10.1039/C8SC04228D
Cl
Reaction #400591
DOI: 10.1039/C8SC04228D
Cc1ccc(CC(=O)N2CCC3(CC2)CN(C2CCc4cc(-c5ncccn5)ccc42)C3)c(C(=O)O)c1
Reaction #757139
DOI: 10.1039/C8SC04228D
COc1ccc(CC(=O)N2CCC3(CC2)CN(C2CCc4cc(-c5ncccn5)ccc42)C3)cc1
Reaction #766401
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2(CC1)CN(C1CCc3cc(-c4ncccn4)ccc31)C2
Reaction #774908
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2(CC1)CN(C1CCc3cc(Br)ccc31)C2
Reaction #888053
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2(CC1)CN(C1CCc3cc(-c4ccc(C(N)=O)nc4)ccc31)C2
Reaction #1324961
DOI: 10.1039/C8SC04228D
O=C(Cc1ccc(C2CC2)cc1)N1CCC2(CC1)CN(C1CCc3cc(-c4ncccn4)ccc31)C2
Reaction #1651687
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2(CC1)CN([C@@H]1CCc3cc(Br)ccc31)C2
Reaction #2000633
desired product
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cnc(-c2ccc3c(c2)CC[C@H]3N2CC3(CCN(C(=O)OC(C)(C)C)CC3)C2)nc1
Reaction #2000634
desired product ( 3-1b )
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cnc(-c2ccc3c(c2)CC[C@H]3N2CC3(CCNCC3)C2)nc1.Cl.Cl
Reaction #2000635
light yellow solid ( 3-1c )
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2(CC1)CN([C@@H]1CCc3cc(-c4ncccn4)ccc31)C2
Reaction #2000636
title compound
Ausbeute 78.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.c1cnc(-c2ccc3c(c2)CC[C@@H]3N2CC3(CCNCC3)C2)nc1
Reaction #2000637
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccc3c(c2)CCC3N2CC3(CCNCC3)C2)ncn1.Cl.Cl
Reaction #2000638
2-[5-(6-methyl-pyrimidin-4-yl)-indan-1-yl]-2,7-diaza-spiro[3.5]nonane-dihydrochloride
Ausbeute 99.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccc3c(c2)CCC3N2CC3(CCNCC3)C2)ncn1.Cl.Cl
Reaction #2000639
2-[5-(6-methyl-pyrimidin-4-yl)-indan-1-yl]-2,7-diaza-spiro[3.5]nonane-dihydrochloride
Ausbeute 102.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2(CC1)CN([C@@H]1CCc3cc(-c4ccc(C(N)=O)cc4)ccc31)C2
Reaction #2000640
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
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