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802264

CN1CCN(C(=O)c2ccc(-c3cnc4c(n3)N(Cc3c(F)ccc(F)c3Cl)CCN4)cc2)CC1
Reaction #167723
{4-[8-(2-chloro-3,6-difluorobenzyl)-5,6,7,8-tetrahydropyrazino[2,3-b]pyrazin-2-yl]phenyl}(4-methylpiperazin-1-yl)methanone
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(C(=O)c2ccc(-c3cnc4[nH]cc(-c5ccc(C(N)=O)cc5)c4c3)cc2)CC1
Reaction #172234
title compound
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)c2ccc(-c3cnc4c(c3)N(C(=O)c3cc(F)ccc3F)CCN4)cc2)CC1
Reaction #179029
DOI: 10.1039/C8SC04228D
CC(c1cc(F)c(F)cc1F)N1CCNc2ncc(-c3ccc(C(=O)N4CCN(C)CC4)cc3)cc21
Reaction #192209
DOI: 10.1039/C8SC04228D
CN1CCN(C(=O)c2ccc(-c3cnc4c(c3)N(Cc3cc(F)ccc3F)C(=O)C(C)(C)N4)cc2)CC1
Reaction #225800
DOI: 10.1039/C8SC04228D
CN1CCN(C(=O)c2ccc(-c3cnc4c(c3)N(Cc3cc(F)c(F)cc3F)CCN4)cc2)CC1
Reaction #237176
DOI: 10.1039/C8SC04228D
CCN1CCN(C(=O)c2ccc(-c3cnc4cccc(Br)c4n3)cc2C)CC1
Reaction #303914
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)c2ccc(-c3cnc4c(c3)N(Cc3c(F)ccc(F)c3Cl)CCN4)cc2)CC1
Reaction #368571
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCN(C(=O)c2ccc(-c3cnc4[nH]cc(-c5ccc(C(N)=O)cc5)c4c3)cc2)CC1
Reaction #420358
title compound
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)c2ccc(-c3cnc4c(c3)N(Cc3cc(F)c(F)cc3F)C(=O)CN4)cc2)CC1
Reaction #746546
title compound
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)c2ccc(-c3cnc4c(c3)N(Cc3cc(F)c(F)cc3F)CCN4)cc2)CC1
Reaction #746547
title compound
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)c2ccc(-c3cnc4c(c3)N(C(=O)c3cc(F)ccc3F)CCN4)cc2)CC1
Reaction #746549
title compound
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)c2ccc(-c3cnc4c(c3)N(Cc3cc(F)ccc3F)C(=O)C(C)(C)N4)cc2)CC1
Reaction #746553
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)c2ccc(-c3cnc4c(c3)N(Cc3cc(F)ccc3F)CC(C)(C)N4)cc2)CC1
Reaction #746554
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)c2ccc(-c3cnc4c(c3)N(Cc3c(F)ccc(F)c3Cl)CCN4)cc2)CC1
Reaction #746559
title compound
Ausbeute 17.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)c2ccc(-c3cnc4c(c3)N(Cc3cc(Cl)ccc3Cl)CCN4)cc2)CC1
Reaction #746583
title compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(c1cc(F)c(F)cc1F)N1CCNc2ncc(-c3ccc(C(=O)N4CCN(C)CC4)cc3)cc21
Reaction #746591
title compound
Ausbeute 2.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)c2ccc(-c3cnc4c(c3)C(O)CCN4)cc2)CC1
Reaction #746636
title compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCN(C(=O)c2ccc(-c3cncc(Br)c3)cc2)CC1
Reaction #1023620
DOI: 10.1039/C8SC04228D
CC(C)CNC(=O)c1cc(Cl)c(CC2CCN(C3CCc4n[nH]cc4C3)C2=O)c(Cl)c1
Reaction #1101026
3,5-Dichloro-N-isobutyl-4-[2-oxo-1-(4,5,6,7-tetrahydro-2H-indazol-5-yl)-pyrrolidin-3-ylmethyl]-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
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