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1373347

O=C(OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1)N1CCN(C(=O)C2CCCCC2)CC1
Reaction #55357
2-(7-Chloro-1,8-naphthyridin-2-yl)-3-(4-cyclohexylcarbonylpiperazin-1-yl)carbonyloxy-isoindolin-1-one
Ausbeute 69.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1)N1CCN(C(=O)C(F)(F)F)CC1
Reaction #55358
2-(7-Chloro-1,8-naphthyridin-2-yl)-3-(4-trifluoroacetylpiperazin-1-yl)carbonyloxy-isoindolin-1-one
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)OC2c3cc(Cl)ccc3C(=O)N2c2ccc3ccc(Cl)nc3n2)CC1
Reaction #346832
3-(4methylpiperazin-1-yl)carbonyloxy-5-chloro- 2-(7-chloro-1,8-naphthyridin-2-yl)isoindolin-1-one
Ausbeute 59.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1)N1CCNCC1
Reaction #346834
2-(7-chloro-1,8-naphthyridin-2-yl)-3-(piperazin-1-yl)carbonyloxy-isoindolin-1-one
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)OC2c3cc(Cl)ccc3C(=O)N2c2ccc3ccc(Cl)nc3n2)CC1
Reaction #415453
3-(4-methylpiperazin-1-yl)carbonyloxy- 5-chloro-2-(7-chloro-1,8-naphthyridin-2-yl)isoindolin-1-one
Ausbeute 59.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1)N1CCNCC1
Reaction #415456
2-(7-chloro-1,8-naphthyridin-2-yl)-3-(piperazin-1-yl)carbonyloxy-isoindolin-1-one
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)OC2c3ccc(C(F)(F)F)cc3C(=O)N2c2ccc3ccc(Cl)nc3n2)CC1
Reaction #415470
2-(7-chloro1,8-naphthyridin-2-yl)-3-(4-methyl-piperazinyl)carbonyloxy-6-trifluoromethyl-1-isoindolinone
Ausbeute 73.5%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)OC2c3cc(Cl)ccc3C(=O)N2c2ccc3ccc(Cl)nc3n2)CC1
Reaction #1627756
DOI: 10.1039/C8SC04228D
O=C(OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1)N1CCNCC1
Reaction #2230304
DOI: 10.1039/C8SC04228D