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8675

O=C1c2ccccc2C(=O)N1CCCl
Reaction #5368
N-(2-chloroethyl)-phthalimide
Ausbeute 65.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCSc1cccc2nccn12
Reaction #5546
desired product
Ausbeute 61.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCSc1ccccn1
Reaction #6180
desired compound
Ausbeute 46.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCOc1ccncc1
Reaction #6244
desired compound
Ausbeute 3.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C1CCN(CCN2C(=O)c3ccccc3C2=O)CC1
Reaction #10543
title compound
Ausbeute 54.4%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccnc(SCCN2C(=O)c3ccccc3C2=O)n1
Reaction #63075
4-amino-2-(2-phthalimidoethylthio)pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCn1cc2c(-c3ccccc3)c(-c3ccncc3)c(-c3ccccc3)nc2n1
Reaction #70879
title compound
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCBr
Reaction #73912
2-(2-bromoethyl)isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CCN1C(=O)c2ccccc2C1=O)OCC
Reaction #73913
diethyl 2-(1,3-dioxoisoindolin-2-yl)ethylphosphonate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2ncnc(N3CCC(n4c(=O)c5cc([N+](=O)[O-])ccc5n(CCN5C(=O)c6ccccc6C5=O)c4=O)CC3)c2cc1OC
Reaction #83319
Compound 33
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCN1CCN(c2n[nH]c3ccccc23)CC1
Reaction #83974
N-[2-[4-(1H-indazol-3-yl)-1-piperazinyl]ethyl]phthalimide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCSc1ccc(O)c([N+](=O)[O-])c1
Reaction #174507
DOI: 10.1039/C8SC04228D
O=C1c2ccccc2C(=O)N1CCN1CCN(c2cccc3ccccc23)CC1
Reaction #177907
DOI: 10.1039/C8SC04228D
O=C1c2ccccc2C(=O)N1CCBr
Reaction #183562
DOI: 10.1039/C8SC04228D
CC1C(Nc2cnn(CCN3C(=O)c4ccccc4C3=O)c(=O)c2Br)CC2CC1C2(C)C
Reaction #184796
DOI: 10.1039/C8SC04228D
O=C1c2ccccc2C(=O)N1CCN1CCN(c2n[nH]c3cc(F)ccc23)CC1
Reaction #203973
DOI: 10.1039/C8SC04228D
O=C1c2ccccc2C(=O)N1CCN1CCN(C(c2ccccc2)c2cccnc2)CC1
Reaction #206974
DOI: 10.1039/C8SC04228D
O=C1c2ccccc2C(=O)N1CCN1CCN2c3ccc(Cl)cc3Cc3ccccc3[C@@H]2C1
Reaction #216924
title compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCN1CCN2c3ccccc3Cn3cccc3[C@@H]2C1
Reaction #216925
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCN1CCN2c3ccc(F)cc3Cc3ccccc3[C@@H]2C1
Reaction #216926
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
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