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1429581

CCOC(=O)CNS(=O)(=O)c1ccc2cc(Cl)ccc2c1
Reaction #53315
title compound
Ausbeute 101.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)NC1(CN2CCN(S(=O)(=O)c3ccc4cc(Cl)ccc4c3)CC2=O)CCN(c2ccnc(C)c2)CC1
Reaction #191306
DOI: 10.1039/C8SC04228D
O=S([O-])c1ccc2cc(Cl)ccc2c1
Reaction #235559
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CN(C(=O)OC(C)(C)C)CCN1S(=O)(=O)c1ccc2cc(Cl)ccc2c1
Reaction #256315
DOI: 10.1039/C8SC04228D
COC(CNS(=O)(=O)c1ccc2cc(Cl)ccc2c1)OC
Reaction #261417
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCN(S(=O)(=O)c2ccc3cc(Cl)ccc3c2)CC1
Reaction #263182
DOI: 10.1039/C8SC04228D
O=C(O)CNS(=O)(=O)c1cc2ccc(Cl)cc2cc1Cl
Reaction #347414
objective compound
Ausbeute 80.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(S(=O)(=O)c2ccc3cc(Cl)ccc3c2)CC1
Reaction #365728
1-(tert-butoxycarbonyl)-4-(6-chloro-naphthalene-2-sulfonyl)piperazine
Ausbeute 91.7%DOI: 10.6084/m9.figshare.5104873.v1
O=S([O-])c1ccc2cc(Cl)ccc2c1.[Na+]
Reaction #433845
sodium 6-chloronaphth-2-ylsulphinate
Ausbeute 96.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CN(C(=O)OC(C)(C)C)CCN1S(=O)(=O)c1ccc2cc(Cl)ccc2c1
Reaction #439921
4-tert-Butoxycarbonyl-1-[(6-chloronaphthalen-2-yl)sulfonyl]-2-ethoxycarbonylpiperazine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C(C)(C)C1
Reaction #440010
4-(tert-Butoxycarbonyl)-1-[(6-chloronaphthalen-2-yl)sulfonyl]-2,2-dimethylpiperazine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(S(=O)(=O)c2ccc3cc(Cl)ccc3c2)CC1
Reaction #518706
1-boc-4-(6-Chloronaphthalen-2-ylsulfonyl)piperazine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NN1CCN(S(=O)(=O)c2ccc3cc(Cl)ccc3c2)CC1=O
Reaction #783096
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCN(S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C(C)(C)C1
Reaction #912003
DOI: 10.1039/C8SC04228D
CCOC(=O)CNS(=O)(=O)c1ccc2cc(Cl)ccc2c1
Reaction #913643
DOI: 10.1039/C8SC04228D
O=C(O)CNS(=O)(=O)c1cc2ccc(Cl)cc2cc1Cl
Reaction #923141
DOI: 10.1039/C8SC04228D
N#Cc1ccc(CN2CCN(S(=O)(=O)c3ccc4cc(Cl)ccc4c3)CC2=O)cc1
Reaction #1039680
DOI: 10.1039/C8SC04228D
CN(C)Cc1ccccc1-c1ccc(N2CCN(Cc3ccccc3)CC(NS(=O)(=O)c3ccc4cc(Cl)ccc4c3)C2=O)cc1
Reaction #1053650
sulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CN(C(=O)OC(C)(C)C)CCN1S(=O)(=O)c1ccc2cc(Cl)ccc2c1
Reaction #1148193
4-tert-Butoxycarbonyl-1-[(6-chloronaphthalen-2-yl)sulfonyl]-2-ethoxycarbonylpiperazine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CNS(=O)(=O)c1cc2ccc(Cl)cc2cc1Cl
Reaction #1171598
objective compound
Ausbeute 80.8%DOI: 10.6084/m9.figshare.5104873.v1
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