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771962

O=C(Oc1ccccc1)OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1
Reaction #55351
2-(7-chloro-1,8-naphthyridin-2-yl)-3-phenoxycarbonyloxy-isoindolin-1-one
Ausbeute 80.7%DOI: 10.6084/m9.figshare.5104873.v1
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
—
Reaction #73803
base
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN(C(=O)N[C@@H](C)c2ccc(Cl)cc2)c2ccc(C3CCCCC3)cc2)cc1
Reaction #77823
4-[3-[1(S)-(4-Chlorophenyl)ethyl]1-(4-cyclohexylphenyl)ureidomethyl]benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccccc1CN(CCc1ccc(Cl)cc1)C1CCN(c2nnc(N)[nH]2)CC1
Reaction #88062
Methyl 2-(((1-(5-amino-4H-1,2,4-triazol-3-yl)piperidin-4-yl)(4-chlorophenethyl)amino)-methyl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #88063
solid
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Oc1ccccc1)OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1
Reaction #94608
2-(7-chloro-1,8-naphthyridin-2-yl)-3-phenoxycarbonyloxy-isoindolin-1-one
Ausbeute 80.7%DOI: 10.6084/m9.figshare.5104873.v1
CCN
Reaction #94609
ethylamine
DOI: 10.6084/m9.figshare.5104873.v1
CCCNC(=O)OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1
Reaction #94610
2-(7-chloro-1,8-naphthyridin-2-yl)-3-propylaminocarbonyloxy-isoindolin-1-one
Ausbeute 178.4%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)NC(=O)OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1
Reaction #94611
2-(7-Chloro-1,8-naphthyridin-2-yl)-3-sec-butylaminocarbonyloxy-isoindolin-1-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CC1)OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1
Reaction #94612
2-(7-chloro-1,8-naphthyridin-2-yl)-3-cyclopropylaminocarbonyloxy-isoindolin-1-one
Ausbeute 81.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCNC(=O)OC1c2cc(C(F)(F)F)ccc2C(=O)N1c1ccc2ccc(Cl)nc2n1
Reaction #94620
3-n-butylaminocarbonyloxy-2-(7-chloro-1,8-naphthyridin-2-yl)-5-trifluoromethyl-isoindolin-1-one
DOI: 10.6084/m9.figshare.5104873.v1
N[C@H]1CC[C@@H](Oc2ccc3nnc(-c4c(Cl)cccc4Cl)n3c2)c2ccccc21
Reaction #162795
title compound
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(NC(=O)N[C@H]2CC[C@@H](Oc3ccc4nnc(-c5c(Cl)cccc5Cl)n4c3)c3ccccc32)n(CCO)n1
Reaction #162796
title compound
Ausbeute 14.3%DOI: 10.6084/m9.figshare.5104873.v1
N[C@H]1CC[C@@H](Oc2ccc3nnc(-c4ccccc4Cl)n3c2)c2ccccc21
Reaction #162800
title compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(NC(=O)N[C@H]2CC[C@@H](Oc3ccc4nnc(-c5ccccc5Cl)n4c3)c3ccccc32)n(CCO)n1
Reaction #162801
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(NC(=O)N[C@H]2CC[C@@H](Oc3ccc4nnc(-c5c(Cl)cccc5Cl)n4c3)c3ccccc32)n(CCCO)n1
Reaction #162809
title compound
Ausbeute 77.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)NC2COCc3ccccc32)cn1
Reaction #170368
title compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCc1ccc(Nc2ccc(C(F)(F)F)cc2NC(=O)c2cc(Cl)c(Cl)cc2C(=O)O)cc1
Reaction #205019
DOI: 10.1039/C8SC04228D
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