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171862

O=C(c1ccc(-c2cnc3c(n2)N(Cc2c(F)ccc(F)c2Cl)CCN3)cc1)N1CCC(N2CCCC2)CC1
Reaction #167729
{4-[8-(2-chloro-3,6-difluorobenzyl)-5,6,7,8-tetrahydropyrazino[2,3-b]pyrazin-2-yl]phenyl}[4-(pyrrolidin-1-yl)piperidin-1-yl]methanone
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(C(=O)N3CCC(N4CCCC4)CC3)cc2)OC1(C)C
Reaction #167730
boronic acid
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(-c2cnc3c(c2)N(Cc2cc(Cl)ccc2Cl)C(=O)CN3)cc1)N1CCC(N2CCCC2)CC1
Reaction #245752
DOI: 10.1039/C8SC04228D
O=C(c1ccc(-c2cnc3c(c2)N(C(=O)Cc2cc(F)ccc2F)CCN3)cc1)N1CCC(N2CCCC2)CC1
Reaction #251684
DOI: 10.1039/C8SC04228D
O=C(c1ccc(-c2cnc3c(c2)N(Cc2c(Cl)cccc2Cl)C(=O)CN3)cc1)N1CCC(N2CCCC2)CC1
Reaction #299765
DOI: 10.1039/C8SC04228D
O=C(c1ccc(-c2cnc3c(c2)N(Cc2c(F)ccc(F)c2Cl)CCN3)cc1)N1CCC(N2CCCC2)CC1
Reaction #746555
title compound
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(-c2cnc3c(c2)N(C(=O)Cc2ccccc2)CCN3)cc1)N1CCC(N2CCCC2)CC1
Reaction #746565
title compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(-c2cnc3c(c2)N(C(=O)Cc2cc(F)ccc2F)CCN3)cc1)N1CCC(N2CCCC2)CC1
Reaction #746568
title compound
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(-c2cnc3c(c2)N(Cc2cc(Cl)ccc2C(F)(F)F)CCN3)cc1)N1CCC(N2CCCC2)CC1
Reaction #746571
title compound
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(-c2cnc3c(c2)N(Cc2cc(Cl)ccc2Cl)C(=O)CN3)cc1)N1CCC(N2CCCC2)CC1
Reaction #746594
title compound
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(-c2cnc3c(c2)N(Cc2cc(Cl)ccc2Cl)CCN3)cc1)N1CCC(N2CCCC2)CC1
Reaction #746595
title compound
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(-c2cnc3c(c2)N(Cc2c(Cl)cccc2Cl)C(=O)CN3)cc1)N1CCC(N2CCCC2)CC1
Reaction #746596
title compound
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(-c2cnc3c(c2)N(Cc2c(Cl)cccc2Cl)CCN3)cc1)N1CCC(N2CCCC2)CC1
Reaction #746597
title compound
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(-c2cnc3c(c2)N(Cc2cc(Cl)ccc2C(F)(F)F)CCN3)cc1)N1CCC(N2CCCC2)CC1
Reaction #908727
DOI: 10.1039/C8SC04228D
O=C(c1ccc(-c2cnc3c(c2)N(C(=O)Cc2ccccc2)CCN3)cc1)N1CCC(N2CCCC2)CC1
Reaction #1027189
DOI: 10.1039/C8SC04228D
O=C(c1ccc(-c2cnc3c(c2)N(Cc2c(F)ccc(F)c2Cl)CCN3)cc1)N1CCC(N2CCCC2)CC1
Reaction #1219478
DOI: 10.1039/C8SC04228D
O=C(c1ccc(-c2cnc3c(c2)N(Cc2c(Cl)cccc2Cl)CCN3)cc1)N1CCC(N2CCCC2)CC1
Reaction #1230055
DOI: 10.1039/C8SC04228D
O=C(c1ccc(-c2cnc3c(c2)N(Cc2cc(Cl)ccc2Cl)CCN3)cc1)N1CCC(N2CCCC2)CC1
Reaction #1648804
DOI: 10.1039/C8SC04228D
O=C(c1ccc(-c2cnc3c(c2)N(Cc2c(F)ccc(F)c2Cl)CCN3)cc1)N1CCC(N2CCCC2)CC1
Reaction #1906210
title compound
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(-c2cnc3c(c2)N(C(=O)Cc2ccccc2)CCN3)cc1)N1CCC(N2CCCC2)CC1
Reaction #1906220
title compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
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