Substructure Search

3253

c1ccc2ncc(C34CCCN3CCC4)cc2c1
Reaction #3382
solid
Yield 48.5%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(O)(c2cnc3ccccc3c2)CC1
Reaction #5063
expected product
Yield 53.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc2ccccc2c1
Reaction #7231
3-methoxyquinoline
Yield 6.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)OC(C)(C)C)C(=O)c1cnc2ccccc2c1
Reaction #41430
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2ncc(Nc3cc4c5c(c3)[C@@H]3CNCC[C@@H]3N5CCOC4)cc2c1
Reaction #51548
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2cnc3ccccc3c2)CC1
Reaction #61456
title product
DOI: 10.6084/m9.figshare.5104873.v1
COC(OC)C(=O)c1cnc2ccccc2c1
Reaction #63023
title product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(Cc1ccc2c(c1)OCCO2)C1CCN(CCn2c(=O)c(Br)cc3ccccc32)CC1
Reaction #68158
tert-butyl (2,3-dihydro-1,4-benzodioxin-6-ylmethyl)(1-(2-(3-bromo-2-oxoquinolin-1(2H)-yl)ethyl)piperidin-4-yl)carbamate
Yield 66.9%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1c(Br)cc2ccccc2n1CCN1CCC(NCc2ccc3c(c2)OCCO3)CC1
Reaction #68159
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-3-bromoquinolin-2(1H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(CN3CCCC4(CCN(c5cnc6ccccc6c5)CC4)C3=O)c3ccccc32)cc1
Reaction #69852
title compound
Yield 72.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C)ccc1Nc1cnc2ccccc2c1
Reaction #70341
Ethyl 5-methyl-2-(quinolin-3-ylamino)benzoate
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc2ccccc2c1
Reaction #73099
quinoline-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2ncc(Nc3cc4c5c(c3)[C@@H]3CNCC[C@@H]3N5CCOC4)cc2c1
Reaction #75830
title compound
DOI: 10.6084/m9.figshare.5104873.v1
OCCC#Cc1cnc2ccccc2c1
Reaction #81917
oil
Yield 136.9%DOI: 10.6084/m9.figshare.5104873.v1
Oc1c(Br)cnc2ccccc12
Reaction #156226
title compound
Yield 71.3%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2ccccc2cc1Br
Reaction #156227
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=O)C(C)(C)C(=O)N(C)c2cc(OCCCn3c(=O)c(Br)cc4ccccc43)ccc21
Reaction #156241
title compound
Yield 51.1%DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=O)C(C)(C)C(=O)N(C)c2cc(OCCCn3c(=O)c(-c4ccccc4)cc4ccccc43)ccc21
Reaction #156243
title compound
Yield 68.4%DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccnc2ccccc12
Reaction #159823
4-Hydroxyquinoline
DOI: 10.6084/m9.figshare.5104873.v1
[O-][n+]1cc(Br)cc2ccccc21
Reaction #161679
3-bromoquinoline-1-oxide
DOI: 10.6084/m9.figshare.5104873.v1
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