Ähnlichkeitssuche

71004

CN1CCN(c2ccc(Nc3ncc(-c4ccc(C(N)=O)c(F)c4)n4ccnc34)cc2)CC1
Reaction #235715
DOI: 10.1039/C8SC04228D
CN1CCN(c2ccc(Nc3ccc(-c4ccc(C(N)=O)c(F)c4)n4ncnc34)cc2)CC1
Reaction #257233
DOI: 10.1039/C8SC04228D
Cc1ccc(C(=O)O)cc1-c1nc(N2CCC(N3CCC(C)CC3)CC2)nc2c1ccc(=O)n2-c1c(F)cccc1F
Reaction #310231
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(COc2ccc(Nc3ncc(-c4ccc(C(N)=O)c(F)c4)n4ccnc34)cc2)CC1
Reaction #376870
DOI: 10.1039/C8SC04228D
—
Reaction #485061
solid
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(B2OC(C)(C)C(C)(C)O2)ccc1OC(F)F
Reaction #508913
2-Difluoromethoxy-N-methyl-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(B2OC(C)(C)C(C)(C)O2)ccc1OC(F)F
Reaction #508914
desired product
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #520753
solid
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(-c2ccc(C)nc2)ccc1Cl
Reaction #544049
title compound
Ausbeute 31.5%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(B2OC(C)(C)C(C)(C)O2)ccc1OC(F)F
Reaction #600181
2-Difluoromethoxy-N-methyl-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(B2OC(C)(C)C(C)(C)O2)ccc1OC(F)F
Reaction #600182
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(B2OC(C)(C)C(C)(C)O2)ccc1OC(F)F
Reaction #687461
2-Difluoromethoxy-N-methyl-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(B2OC(C)(C)C(C)(C)O2)ccc1OC(F)F
Reaction #687462
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1nc(-c2ccc(Cl)c(C(=O)OC)c2)cnc1N
Reaction #733873
methyl 5-{5-amino-6-[(methylamino)carbonyl]pyrazin-2-yl}-2-chlorobenzoate
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(c2nc3cc(-c4ccc(C(N)=O)c(Cl)c4)ccc3o2)CC1
Reaction #797317
titled compound
Ausbeute 13.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(=O)N1CCC(c2nc3cc(-c4ccc(C(N)=O)c(Cl)c4)ccc3o2)CC1
Reaction #797329
titled compound
Ausbeute 16.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(c2ccc3oc(-c4ccc(C(N)=O)c(F)c4)nc3c2)CC1
Reaction #797366
titled compound
Ausbeute 6.8%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1nc(-c2ccc(Cl)c(C(=O)OC)c2)cnc1N
Reaction #909826
DOI: 10.1039/C8SC04228D
Cc1cc(-c2cnnc(Cn3ccnc3C)c2)ccc1Cl.Cl
Reaction #979083
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(Nc3ccc(-c4ccc(C(N)=O)c(F)c4)n4ncnc34)cc2)CC1
Reaction #1098456
title compound
Ausbeute 18.4%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter