Substructure Search

15559

O=C1CCCN1CCCNc1c([N+](=O)[O-])cnc2cc(Br)ccc12
Reaction #9491
1-[3-(7-bromo-3-nitroquinolin-4-ylamino)propyl]pyrrolidin-2-one
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCc1nc2cnc3cc(Br)ccc3c2n1CCCN1CCCC1=O
Reaction #9492
1-{3-[7-bromo-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]propyl}pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCN1CCCNc1c([N+](=O)[O-])cnc2ccc(Br)cc12
Reaction #9493
1-[3-(6-bromo-3-nitroquinolin-4-ylamino)propyl]pyrrolidin-2-one
Yield 87.8%DOI: 10.6084/m9.figshare.5104873.v1
COCCc1nc2cnc3ccc(Br)cc3c2n1CCCN1CCCC1=O
Reaction #9494
1-{3-[8-bromo-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]propyl}pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc2cnc3cc(-c4ccccc4)ccc3c2n1CCCN1CCCC1=O
Reaction #9507
1-[3-(2-ethoxymethyl-7-phenyl-1H-imidazo[4,5-c]quinolin-1-yl)propyl]pyrrolidin-2-one
Yield 56.7%DOI: 10.6084/m9.figshare.5104873.v1
COCCc1nc2cnc3cc(-c4ccccc4)ccc3c2n1CCCN1CCCC1=O
Reaction #9508
1-{3-[2-(2-methoxyethyl)-7-phenyl-1H-imidazo[4,5-c]quinolin-1-yl]propyl}pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)N(C2CCCN(C(N)=O)CC2)CC1COc1ccc(C#N)cn1
Reaction #44483
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCS(=O)(=O)c1ccc2cc(Cl)ccc2c1)N1CCC(N2CCCC2=O)CC1
Reaction #48493
title compound
Yield 39.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCN1CCCC1=O)[C@@H]1CCCN1C(=O)OCc1ccccc1
Reaction #93118
(S)-1-benzyloxycarbonyl-N-[3-(2-oxo-pyrrolidinyl)propyl]-2-pyrrolidine carboxamide
Yield 29.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCN1CCCC1=O)[C@@H]1CCCN1
Reaction #93119
(S)-N-[3-(2-oxo-1-pyrrolidinyl)propyl]-2-pyrrolidinecarboxamide
Yield 71.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1c[nH]cn1)C(=O)N1CCC[C@H]1C(=O)NCCCN1CCCC1=O)OCc1ccccc1
Reaction #93120
Nα -benzyloxycarbonyl-L-histidyl-N-[3-(2-oxo-1-pyrrolidinyl)-propyl]-L-prolinamide
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #93639
B7
DOI: 10.6084/m9.figshare.5104873.v1
N[C@H]1CCC[C@@H](N2CCCC2=O)C1
Reaction #162155
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCN1CCCN1CCN(c2cccc(Cl)c2)CC1
Reaction #182092
DOI: 10.1039/C8SC04228D
CCN(CCCN1CCCC1=O)Cc1cccc(OC)c1-c1cccc(CC(=O)OC)c1
Reaction #182146
DOI: 10.1039/C8SC04228D
CCc1ccc(N2CCN(CCCN3CCCC3=O)CC2)cc1
Reaction #197953
DOI: 10.1039/C8SC04228D
COC(=O)c1sc(C2=CCCCC2)cc1NC1CCN2C(=O)CCC2C1
Reaction #199372
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(N2CCC(Cc3c(Cl)cc(-c4ccc(C(=O)N5CCC(C(F)(F)F)CC5)cc4)cc3Cl)C2=O)CC1
Reaction #207990
DOI: 10.1039/C8SC04228D
COC1CCC(N2CCC(Nc3ncnc4ccc(C(F)(F)F)cc34)C2=O)C(CNC(C)=O)C1
Reaction #213776
DOI: 10.1039/C8SC04228D
CC1(N2CCC(N3C(=O)CC4CCCCC43)CC2)CCN(C(=O)C2CC2)CC1
Reaction #223042
DOI: 10.1039/C8SC04228D
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