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C1CCN(C1)CCCCl

FC(F)(F)c1ccc([C@]23C[C@H]2CN(CCCCl)C3)cc1
Reaction #40930
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(-c2cn(CCCN3C[C@@H]4C[C@]4(c4ccc(C(F)(F)F)cc4)C3)c(=O)[nH]c2=O)n1.Cl.Cl
Reaction #41056
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1-c1cn(CCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)c(=O)[nH]c1=O.Cl
Reaction #41057
title compound
Ausbeute 62.5%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc([C@]23C[C@H]2CN(CCCCl)C3)cc1
Reaction #47938
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(C(F)(F)F)ccc1[C@]12C[C@H]1CN(CCCCl)C2
Reaction #47948
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)O)ccc1OCCCN1CCCC1.Cl
Reaction #51056
3-methoxy-4-(3-pyrrolidin-1-ylpropoxy)benzoic acid hydrochloride
Ausbeute 77.3%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2c(c1)cnn2-c1ccc(OCCCN2CCCC2)cc1
Reaction #173206
DOI: 10.1039/C8SC04228D
ClCCCN1CCCC1
Reaction #173740
DOI: 10.1039/C8SC04228D
CN(C)CC1(c2cccc(OCCCN3CCCC3)c2)CCOCC1
Reaction #178028
DOI: 10.1039/C8SC04228D
O=C1CCCN1CCCN1CCN(c2cccc(Cl)c2)CC1
Reaction #182092
DOI: 10.1039/C8SC04228D
Fc1ccc(Nc2ncnc3ccc(OCCCN4CCCC4)cc23)cc1Cl
Reaction #185569
DOI: 10.1039/C8SC04228D
ClCC1CN2CCCC2CO1
Reaction #196228
DOI: 10.1039/C8SC04228D
CCc1ccc(N2CCN(CCCN3CCCC3=O)CC2)cc1
Reaction #197953
DOI: 10.1039/C8SC04228D
c1ccc2[nH]ncc2c1
Reaction #205182
DOI: 10.1039/C8SC04228D
Cc1cc(CO)n(-c2ccc(OCCCN3CCCC3)cc2)n1
Reaction #206893
DOI: 10.1039/C8SC04228D
Cc1ccc2c(n1)N(CCCN1CCCC1)c1ccccc1N(C)C2=O
Reaction #208354
DOI: 10.1039/C8SC04228D
c1ccc2c(-c3ccc(OCCCN4CCCC4)cc3)c3c(nc2c1)CCCC3
Reaction #213108
DOI: 10.1039/C8SC04228D
N#CC1(c2cccc(OCCCN3CCCC3)c2)CCOCC1
Reaction #213519
DOI: 10.1039/C8SC04228D
O=C(CCl)CN1CCCC1=O
Reaction #222400
DOI: 10.1039/C8SC04228D
Ic1ccc(OCCCN2CCCC2)cc1
Reaction #227678
DOI: 10.1039/C8SC04228D
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