Substructure Search

O=Cc1cc2ccccc2nc1Cl

O=C1c2cc3c(cc2-c2c1c(Cl)nc1ccccc21)OCO3
Reaction #3245
title compound
Yield 59.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c3c(c(Cl)nc2c1)C(=O)c1ccccc1-3
Reaction #3248
title compound
Yield 73.4%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCNc1nc2cc(F)ccc2c2c1C(=O)c1ccccc1-2.Cl.Cl
Reaction #3251
title compound
Yield 68.6%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCOc1nc2ccccc2c2c1C(=O)c1cc3c(cc1-2)OCO3
Reaction #3255
title compound
Yield 68.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc2ccccc2nc1Cl
Reaction #4881
white crystals
Yield 62.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc2ccccc2nc1Cl
Reaction #5219
2-chloro-3-quinolinecarboxaldehyde
Yield 92.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)c2c1c(Cl)nc1ccccc21
Reaction #5225
4-Chloro-furo[3,4-c]quinoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OCc2c1c(Cl)nc1ccccc21
Reaction #5226
4-Chloro-furo[3,4-c]quinolin-3(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OCc2c1cnc1ccccc21
Reaction #5227
Furo[3,4-c]quinolin-3(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc2ccccc2nc1Cl
Reaction #6321
2-chloro-3-quinolinecarboxaldehyde
Yield 92.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2cc(C(=O)O)c(-c3ccccc3)nc2c1
Reaction #8443
7-Methoxy-2-phenyl-quinoline-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc2ccc(SCc3ccc(OC)cc3)cc2nc1OC
Reaction #62603
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2cc(F)c(F)cc2nc1Cl
Reaction #83632
3-ethoxycarbonyl-6,7-difluoro-2-chloroquinoline
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2cc(F)c(F)cc2nc1N(C)CCC#N
Reaction #83633
3-ethoxycarbonyl-6,7-difluoro-2-(N-methyl-N-β-cyanoethylamino)quinoline
Yield 100.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(Cl)c(C#N)cc2c1
Reaction #84104
product
Yield 38.0%DOI: 10.6084/m9.figshare.5104873.v1
OCc1cc2cc(Br)ccc2nc1Cl
Reaction #156249
(6-bromo-2-chloroquinolin-3-yl)methanol
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc2cccc(F)c2nc1Cl
Reaction #162533
1-(2-chloro-8-fluoroquinolin-3-yl)ethanone
Yield 72.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)c1cc2cccc(F)c2nc1Cl
Reaction #162534
(R)-1-(2-chloro-8-fluoroquinolin-3-yl)ethanol
Yield 73.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)c1cc2ccc(F)cc2nc1Cl
Reaction #162539
1-(2-chloro-7-fluoroquinolin-3-yl)-ethanol
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc2ccc(F)cc2nc1Cl
Reaction #162540
1-(2-chloro-7-fluoroquinolin-3-yl)ethanone
Yield 81.5%DOI: 10.6084/m9.figshare.5104873.v1
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