quinolinone

CCC#CCn1c(=O)ccc2c(Cl)cccc21
Reaction #1605
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1c(=O)ccc2c(Cl)cccc21
Reaction #1673
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1c(=O)ccc2c(Cl)cccc21
Reaction #2178
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1c(=O)ccc2c(Cl)cccc21
Reaction #2219
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1c(=O)ccc2c(Cl)cccc21
Reaction #2277
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC(NC(C)C)C(O)c1ccc(OC(=O)C2CCCCC2)c2[nH]c(=O)ccc12
Reaction #56057
8-cyclohexylcarbonyloxy-5-(1-hydroxy-2-isopropylaminobutyl)carbostyril
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCC(NC(C)C)C(O)c1ccc(OC(=O)C2CCCCC2)c2c1CCC(=O)N2
Reaction #56059
8-cyclohexylcarbonyloxy-5-(1-hydroxy-2-isopropylaminobutyl)-3,4-dihydrocarbostyril
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCC(NC(C)C)C(O)c1ccc(OC(=O)c2ccc(C)cc2)c2c1CCC(=O)N2
Reaction #56060
5-(1-hydroxy-2-isopropylaminobutyl)-8-p-methylbenzoyloxy-3,4-dihydrocarbostyril
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
O=c1ccc2ccccc2n1CC1OCCO1
Reaction #67967
1-(1,3-dioxolan-2-ylmethyl)quinolin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=c1ccc2ccccc2n1CCCCl
Reaction #202266
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1ccc(Br)c([N+](=O)[O-])c1
Reaction #260333
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1ccc2ncccc2c1
Reaction #272444
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=c1ccc2ccccc2n1CCCCCl
Reaction #274273
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=c1ccc2ccccc2n1CCCCCCl
Reaction #286992
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)NC1CCN(CCn2c(=O)ccc3ccccc32)CC1
Reaction #342512
product
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
O=c1ccc2ccccc2[nH]1
Reaction #342684
quino- lone
Ausbeute 198.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_10
CC(=O)OC(=O)c1ccccc1
Reaction #365157
benzoyl acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CC(C)(C)OC(=O)NC1CCN(CCn2c(=O)ccc3ccccc32)CC1
Reaction #391718
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=c1[nH]c2cccc3c2n1CC(N(CC1CC1)CC1CC1)C3
Reaction #414668
5-[bis(cyclopropylmethyl)amino]-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
O=c1ccc2ccccc2[nH]1
Reaction #445666
6-(α-pyridiniumacetyl)carbostyril chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_08
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