Involved in 38 reactions

450441

C[C@H]1COc2c(N3CCN(C)CC3)c(F)cc3c(=O)c(C(=O)O)cn1c23.C[C@H]1COc2c(N3CCN(C)CC3)c(F)cc3c(=O)c(C(=O)O)cn1c23.O
Reaction #59651
levofloxacin hemihydrate
Yield 3079.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(C)C(=O)OCn1cc(COc2ccc(-n3cnnn3)nc2)nn1
Reaction #167823
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)COC(=O)C(C)O
Reaction #335794
isobutyl lactate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CC(=O)Nc1ccc(CCc2cnc3c(N)nc4cc(C)ccc4c3c2)cc1
Reaction #427510
N-(4-(2-(5-amino-8-methylbenzo[f][1,7]naphthyridin-2-yl)ethyl)phenyl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
COC(=O)c1ccc(C#Cc2cnc3c(N)nc4cc(C)ccc4c3c2)c(C)c1C
Reaction #427514
methyl methyl-4-((5-amino-8-methylbenzo[f][1,7]naphthyridin-2-yl)ethynyl)-3-methylbenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CCCCC=CC(C)(C)C(=O)O
Reaction #464816
2,2-dimethyl-3-octenoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
CC(=O)OCc1c(-c2cc(Nc3ccc(C4CCN(C)CC4)cn3)c(=O)n(C)n2)cccc1-n1ncc2cc(C(C)(C)C)cc(F)c2c1=O
Reaction #536890
2-(6-tert-butyl-8-fluoro-1-oxophthalazin-2(1H)-yl)-6-(1-methyl-5-(5-(1-methylpiperidin-4-yl)pyridin-2-ylamino)-6-oxo-1,6-dihydropyridazin-3-yl)benzyl acetate
Yield 75.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCP(=O)(O)CCCN
Reaction #663199
ethyl(3-aminopropyl)phosphinic acid
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CCOC(=O)CCc1ccc2c(c1)nc(N)c1ncc(C#Cc3ccc(OCOC)cc3C)cc12
Reaction #718356
ethyl 3-(5-amino-2-((4-(methoxymethoxy)-2-methylphenyl)ethynyl)-benzo[f][1,7]naphthyridin-8-yl)propanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
O=C(c1ccc(-c2ccc(OCc3ccccc3)cc2)nc1)N1CCN(Cc2ccc(F)cc2)CC1
Reaction #962245
Compound 17
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
CCOC(OCC)c1cn(C[Si](C)(C)C)nn1
Reaction #964558
crude title compound
Yield 81.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
CCOC(=O)Cn1cc([C@H](NS(=O)C(C)(C)C)c2ccc(OCC(F)(F)F)cn2)nn1
Reaction #964563
title compound
Yield 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
O=C(c1ccc(-c2ccc(OCc3ccccc3)cc2)nc1)N1CCN(Cc2ccc(F)cc2)CC1
Reaction #965054
Compound 17
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
CCCCC=CC(C)(C)C(=O)O
Reaction #1194895
2,2-dimethyl-3-octenoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_05
CC(=O)Nc1ccc(CCc2cnc3c(N)nc4cc(C)ccc4c3c2)cc1
Reaction #1346378
N-(4-(2-(5-amino-8-methylbenzo[f][1,7]naphthyridin-2-yl)ethyl)phenyl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_06
COC(=O)c1ccc(C#Cc2cnc3c(N)nc4cc(C)ccc4c3c2)c(C)c1C
Reaction #1346382
methyl methyl-4-((5-amino-8-methylbenzo[f][1,7]naphthyridin-2-yl)ethynyl)-3-methylbenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_06
O=CCC1CCCCc2noc(=O)n21
Reaction #1354402
title compound
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
CC(=O)OCc1c(-c2cc(Nc3ccc(C4CCN(C)CC4)cn3)c(=O)n(C)n2)cccc1-n1ncc2cc(C(C)(C)C)cc(F)c2c1=O
Reaction #1518382
2-(6-tert-butyl-8-fluoro-1-oxophthalazin-2(1H)-yl)-6-(1-methyl-5-(5-(1-methylpiperidin-4-yl)pyridin-2-ylamino)-6-oxo-1,6-dihydropyridazin-3-yl)benzyl acetate
Yield 75.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_01
COC(=O)c1ccc2c(C3CCCCC3)c(-c3ccccc3N)n(C[C@H](NC(=O)OC(C)(C)C)C(=O)O)c2c1
Reaction #1531818
3-[2-(2-aminophenyl)-3-cyclohexyl-6-(methoxycarbonyl)-1H-indol-1-yl]-N-(tert-butoxycarbonyl)alanine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_02
CC(=O)Nc1ccc(CCc2cnc3c(N)nc4cc(C)ccc4c3c2)cc1
Reaction #1566797
N-(4-(2-(5-amino-8-methylbenzo[f][1,7]naphthyridin-2-yl)ethyl)phenyl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
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